Free
Meeting Abstracts  |   July 1996
Stimulation of α2Adrenoceptors Dilates the Rat Middle Cerebral Artery
Author Notes
  • (Bryan, Suresh) Associate Professor of Anesthesiology.
  • (Eichler) Technician, Department of Anesthesiology.
  • (Swafford) Associate Professor of Anesthesiology.
  • (Johnson) Assistant Professor of Anesthesiology.
  • (Childres) Professor and Chairman, Department of Anesthesiology.
  • Received from the Department of Anesthesiology, Baylor College of Medicine, Houston, Texas. Submitted for publication January 27, 1995. Accepted for publication February 13, 1996. Supported by National Institutes of Health grant PO1-NS27616. Presented at the annual meeting of the Society for Neuroscience, Miami Beach, Florida, November 13-18, 1994.
  • Address reprint requests to Dr. Bryan: Department of Anesthesiology, Baylor College of Medicine, One Baylor Plaza, Room 434D, Houston, Texas 77030.
Article Information
Meeting Abstracts   |   July 1996
Stimulation of α2Adrenoceptors Dilates the Rat Middle Cerebral Artery
Anesthesiology 7 1996, Vol.85, 82-90. doi:
Anesthesiology 7 1996, Vol.85, 82-90. doi:
Key words: Animals: rats. Artery: cerebral. Gases: nitric oxide. Heart: endothelium. Proteins: G proteins. Receptors: alpha2-adrenergic. Toxins: pertussis.
alpha2-ADRENOCEPTOR agonists, such as clonidine and dexmedetomidine, are useful adjuncts for general anesthesia. Although these agents are more widely used in veterinary than in human anesthesia practice, their potential for use with humans is rapidly becoming recognized. These agents are of interest primarily because of their ability to reduce the requirement for both inhalation and intravenous anesthetics. However, other important actions include anxiety reduction, sedation, analgesia, hemodynamic stabilization, as well as antisialagogic and antiemetic properties. [1] .
As a result of their usefulness in the practice of anesthesiology, the effects of these agonists on the cerebrovascular circulation is an important issue. Previous studies support the idea that alpha2adrenoceptor agonists constrict cerebral arteries and thus decrease cerebral blood flow. [2-6] Dexmedetomidine produced a biphasic contraction in isolated rings of dog middle cerebral artery (MCA). [2] However, the contraction at the larger doses may have been caused by stimulation of alpha1adrenoceptors by dexmedetomidine because it was not blocked by the alpha2adrenoceptor antagonist, atipamezole. [2] Measurement of cerebral blood flow after the administration of clonidine or dexmedetomidine indicates that stimulation of alpha2adrenoceptors decreased cerebral blood flow in anesthetized dogs and cats without a concomitant decrease in the cerebral metabolic rate for oxygen. [3-6] The decrease in cerebral blood flow after the administration of alpha2adrenoceptor agonists may be due, at least in part, to neurally mediated mechanisms produced by altered activity of the locus ceruleus. [6] .
The vasoactive response of alpha adrenoceptor stimulation in cerebral arteries appears to be species dependent. [7] Constriction of cerebral arteries in dogs and cats by norepinephrine is mediated primarily through stimulation of alpha2adrenoceptors, whereas in rats, monkeys, and humans the constriction is mediated through alpha1adrenoceptors. [7] Given the heterogeneity of the alpha adrenoceptor response with different species, it is possible that the direct effects of alpha2adrenoceptor agonists are different for species other than the dog and cat.
Many of the studies involving alpha2adrenoceptors in cerebral arteries were conducted before the realization that endothelium was important in the contraction/relaxation state of the vessel (for review see Edvinsson et al. [7]). For many of these studies, it is not known if the endothelium was preserved during the preparation and investigation of the arteries. As a consequence, alpha2adrenoceptor function involving the endothelium could have been missed or overlooked. In many peripheral vessels, alpha2adrenoceptor stimulation can elicit a dilation or relaxation that requires intact endothelium. [8-11] Furthermore, the constrictor effect of alpha2adrenoceptor on smooth muscle often can mask this vasodilatory effect involving the endothelium. [12,13] In the current study, we tested the hypothesis that cerebral arteries, specifically the rat MCA, like peripheral vessels has an associated alpha2adrenoceptor dilatory function that requires intact endothelium. We show that stimulation of alpha2adrenoceptors in the MCA from the rat produced a dilation. The dilation required intact endothelium and involved nitric oxide and a pertussis toxin-sensitive G protein.
Methods and Materials
The experimental protocol was approved by the Animal Protocol Review Committee at Baylor College of Medicine. Experiments were conducted on approximately 98 MCAs from 49 male Long Evans rats weighing between 270 and 350 g. All rats were housed in the animal holding facility and were allowed free access to food and water before their use.
Harvesting Middle Cerebral Arteries
Rats were placed in a methyl methacrylate polymer anesthetic chamber with 0.25 ml isoflurane and carefully watched. Each rat was decapitated on loss of the righting reflex and lack of a response to tail pinch. The brain was immediately removed and placed in cold physiologic saline solution (PSS; see later for composition). Both the left and right MCAs were carefully removed beginning at the circle of Willis and continuing lateral and dorsal for approximately 5 or 6 mm. A section of the harvested MCA approximately 1 mm long and lying between branch points was mounted as described later.
Arteriograph and Mounting the Middle Cerebral Arteries
We used a relatively new technique for studying isolated vessels. This method may be more physiologically relevant than other in vitro methods because the MCAs were pressurized and luminally perfused. [14] The MCAs were placed in an arteriograph (Living Systems, Burlington, VT) and a micropipet was inserted into each end of the MCA segment. [14,15] The ends of the MCAs were secured to the micropipets with 9-O nylon sutures. After securing the proximal end of each MCA, the lumen was gently perfused with PSS to remove blood and other contents from the lumen before securing the distal end. The arteriograph consisted of two independent chambers: one for each MCA harvested from a single rat. Each MCA was bathed in PSS, which was continually circulated from a reservoir where the solution was equilibrated with a gas consisting of 20% Oxygen2and 5% CO2in a balance of Nitrogen2[14] (Figure 1). The PSS was heated before entering the chamber to maintain a bath temperature of 37 degrees C.
Figure 1. A diagram of the arteriograph for mounting middle cerebral arteries from the rat. The gauge on the tubing at right represents a flow meter for measuring perfusion of physiologic saline through the lumen of the artery; the two remaining gauges on either side of the artery represent pressure transducers for measuring the perfusion pressure across the micropipets and the middle cerebral artery. Transmural pressure could be set by raising the two reservoirs to a height above the middle cerebral artery. Luminal perfusion could be adjusted independently of the transmural pressure by providing a perfusion pressure (Delta P).
Figure 1. A diagram of the arteriograph for mounting middle cerebral arteries from the rat. The gauge on the tubing at right represents a flow meter for measuring perfusion of physiologic saline through the lumen of the artery; the two remaining gauges on either side of the artery represent pressure transducers for measuring the perfusion pressure across the micropipets and the middle cerebral artery. Transmural pressure could be set by raising the two reservoirs to a height above the middle cerebral artery. Luminal perfusion could be adjusted independently of the transmural pressure by providing a perfusion pressure (Delta P).
Figure 1. A diagram of the arteriograph for mounting middle cerebral arteries from the rat. The gauge on the tubing at right represents a flow meter for measuring perfusion of physiologic saline through the lumen of the artery; the two remaining gauges on either side of the artery represent pressure transducers for measuring the perfusion pressure across the micropipets and the middle cerebral artery. Transmural pressure could be set by raising the two reservoirs to a height above the middle cerebral artery. Luminal perfusion could be adjusted independently of the transmural pressure by providing a perfusion pressure (Delta P).
×
Luminal or transmural pressure was maintained at 85 mmHg by raising reservoirs, connected to the micropipets, to the appropriate height above each MCA (Figure 1); luminal perfusion was adjusted to 100 micro liter/min by setting the two reservoirs at different heights. With micropipets equally matched for resistance, the transmural pressure was midway between the pressures generated by the PSS in the two reservoirs; i.e., the sum of Delta P/2 and the pressure generated by the output reservoir (Figure 1). The transmural pressure and the luminal perfusion could be controlled independently. Pressure transducers located between the micropipets and the reservoirs provided a measure of perfusion pressure (Figure 1). A flow meter (#11, Gilmont Instruments, Barrington, IL) connected to the tubing leading to the output reservoir measured luminal flow. The luminal perfusate was gassed in the reservoir. In addition, the luminal perfusate traveled through gas-permeable tubing (Silastic) in the bath before perfusing the lumen of the MCAs to ensure that it was properly gassed and equilibrated to 37 degrees C. In one study, the MCAs were pressurized without having a luminal flow by occluding the outflow tubing. Samples of PSS from the bath were analyzed for partial pressure of oxygen, partial pressure of carbon dioxide, and pH using a Corning model 178 analyzer (Medfield, NY).
Vessels were magnified using an inverted microscope equipped with a video camera and monitor. Outside diameters of the MCAs were measured directly from the video monitor.
General Experimental Outline and Design
Middle cerebral arteries were allowed at least 1 h to stabilize before experiments were conducted. During this time, the diameters decreased to approximately 75% of the initial diameter after pressurization. This development of spontaneous tone was indicative of a healthy artery. For dose-response relaxations, the MCAs were preconstricted by the abluminal addition 10 sup -6 M serotonin. Although dexmedetomidine is the agonist most commonly used for alpha2adrenoceptor studies in the anesthesia literature, we choose UK14,304 as the alpha2agonist for the current studies. We wanted to be consistent with previous studies in peripheral vessels that showed that stimulation of alpha2adrenoceptors by UK14,304 elicited an endothelium-mediated dilation. [10-12,16-18] UK14,304 is a recognized selective agonist for alpha2adrenoceptors having an 1,800-fold greater affinity for the alpha2adrenoceptor than for the alpha1adrenoceptor. [19] Rauwolscine and idazoxan, which are selective antagonists important in the pharmacologic definition of alpha2adrenoceptors, [19] were used to determine the selectivity of UK14,304. UK14,304 does have some affinity for imidazoline receptors; the selectivity for the of alpha2adrenoceptors is 100-fold greater than for imidazoline receptors. [20] .
UK14,304 was cumulatively added to the extraluminal bath at the appropriate concentration. After each dose of UK14,304, an interval of 5 min was allowed before the diameter of the vessel was measured. Antagonists were added 30 min before any study was performed; pertussis toxin (100 ng/ml) was added 2 h before the UK14,304 dose-response curve. [11] In studies where the alpha adrenoceptor antagonists, phentolamine and rauwolscine, were used, the concentration of serotonin applied was 3 x 10 sup -6 M or 10 sup -5 M. Because phentolamine and rauwolscine are weak serotonin antagonists, the concentration of serotonin had to be increased to obtain the same degree of contraction as in the absence of these antagonists. In other studies, the diameters of the MCAs were already decreased by the addition of N-nitro-L-arginine methyl ester (L-NAME) or removal of the endothelium before the addition of serotonin. The addition of 10 sup -6 M serotonin produced even more constriction in the artery. We previously demonstrated that this added constriction did not affect the response to UK14,304. [21] .
Two UK14,304 dose-response curves were obtained for each MCA. In some MCAs, control dose-response curves were followed by a dose-response after the experimental condition (endothelium removal, blocker, etc.). In other MCAs, which served as time controls, two consecutive dose-response curves were run. In studies where the experimental condition could be reversed (i.e., with or without luminal flow), the control and experimental curves were randomized as to the order for each MCA.
After the first dose-response curve, the bath was washed with fresh PSS and the MCA was allowed 30 min to recover before performing the second dose-response curve. Although two MCAs were harvested from each rat, each MCA was used in a different experimental protocol.
In one study, the endothelium was removed by forcing 8 ml air through the lumen of the vessels. [22] Care was taken to ensure that pressure did not exceed 85 mmHg during this process. Removal of the endothelium was confirmed by the absence of a dilation to the addition of 10 sup -5 M acetylcholine.
Reagents and Drugs
UK14,304 (5-bromo-N-(4,5-dihydro-1H-imidazol-2-yl)-6-quinoxalinamine), prazosin, idazoxan, rauwolscine, and S-nitroso-N-acetylpenicillamine were obtained from Research Biochemicals (Natick, MA). L-NAME [NG-nitro-L-arginine methyl ester], L- and D-arginine, phentolamine, serotonin, and pertussis toxin were obtained from Sigma Chemical (St. Louis, MO). Reagents were dissolved in either PSS or distilled water with the following exceptions: 0.25 mg UK14,304 was dissolved in dimethyl sulfoxide/distilled water (0.25 ml/11.15 ml), 8.8 mg S-nitroso-N-acetylpenicillamine was dissolved in dimethyl sulfoxide/water (0.53 ml/2.5 ml), and 21 mg prazosin was dissolved in 5 ml methanol. Dimethyl sulfoxide alone did not change the diameter of the MCAs at the above concentrations for UK14,304 and S-nitroso-N-acetylpenicillamine. In the prazosin studies, the methanol vehicle was added to the control group. Pertussis toxin was in solution (50 micro gram/ml in 50% glycerol, 50 mM Tris, 10 mM glycine, 0.5 M NaCl, pH 7.5) when purchased and was added directly to the bath.
The PSS comprised the following (in mM) [15] : NaCl 119, NaHCO324, KCl 4.7, KH2PO41.18, MgSO41.17, CaCl21.6, glucose 5.5, and EDTA 0.026.
Statistics
Data are expressed as the mean+/-the standard error of the mean with n representing the number of MCAs. Values for the MCAs presented represent the diameters before the addition of serotonin. For comparison of responses to UK14,304, a repeated-measures analysis of variance was used followed by the Fisher test for multiple comparisons when appropriate. The acceptable level of significance was defined as P < 0.05.
Results
The resting outside diameter for MCAs in one study was 239+/- 13 micro meter (n = 8); the resting diameter in the remainder of the studies did not differ statistically from the above value. The abluminal pH level was 7.332+/-0.004 (n = 25), partial pressure of carbon dioxide was 35.0+/-0.5 mmHg (n = 26), and partial pressure of oxygen was 144+/-1 mmHg (n = 25). In preliminary studies, PSS was collected from the input micropipet to determine if the luminal perfusate was correctly gassed (see Arteriograph and Mounting the MCAs in Methods and Materials for the technique of gassing the luminal PSS). There were no significant differences in gasses or pH level between the luminal and abluminal PSS. The mean input and output pressures (n = 25) across the two micropipets and MCAs were 87.1+/-0.2 and 82.9+/-0.2 mmHg, respectively. When the MCAs were preconstricted with 10 sup -6 M serotonin, the vessels constricted approximately 20%. MCAs constricted with serotonin without the addition of UK14,304 were stable (i.e., no significant change in diameter, n = 28) over 30 min. The time required for the UK14,304 dose-response curve was 25 min.
In the first study, we determined the response of abluminally applied UK14,304 in MCAs with flow (100 micro liter/min) and without flow through the lumen (Figure 2(A)). Luminal flow was stopped by occluding the outflow tubing distal to the micropipet and pressure transducer. Regardless of whether or not there was luminal flow, transmural pressure was maintained at 85 mmHg. Two dose-response curves were conducted on each MCA. In half of the arteries (four) the dose-response curve was conducted with flow through the lumen followed by the dose-response curve without flow; the order was reversed for the remaining four MCAs. The response to UK14,304 with "flow" or "no flow" was independent of the order for the concentration-response curves. Therefore, the data were combined for the graphs in Figure 2(A). The mean dilation (% diameter change) at a concentration of 10 sup -4 M UK14,304 in MCAs with and without flow was 11.4+/-1.6% and 9.7+/-1.6% (n = 8 MCAs), respectively. There was no significant difference in the dilations produced by UK14,304 in MCAs with flow or without flow. For the remainder of the studies described later, MCAs were maintained with a luminal flow of 100 micro liter/min.
Figure 2. (A) The percent change in the diameter of the rat middle cerebral artery with increasing concentrations of UK14,304 in MCAs with flow (100 micro liter/min) and without flow (diameter 239+/-13 micro meter, n = 8 middle cerebral arteries). The transmural pressure was maintained at 85 mmHg in all middle cerebral arteries. There was no significant difference in the dilation produced by UK14,304 in middle cerebral arteries with flow or without flow. (B) The percent change in diameter for two consecutive UK14,304 dose-response curves (diameter 233 +/-8 micro meter, n = 6 middle cerebral arteries). There was no significant difference in the dilation produced by UK14,304 between the first (control 1) and second (control 2) curves.
Figure 2. (A) The percent change in the diameter of the rat middle cerebral artery with increasing concentrations of UK14,304 in MCAs with flow (100 micro liter/min) and without flow (diameter 239+/-13 micro meter, n = 8 middle cerebral arteries). The transmural pressure was maintained at 85 mmHg in all middle cerebral arteries. There was no significant difference in the dilation produced by UK14,304 in middle cerebral arteries with flow or without flow. (B) The percent change in diameter for two consecutive UK14,304 dose-response curves (diameter 233 +/-8 micro meter, n = 6 middle cerebral arteries). There was no significant difference in the dilation produced by UK14,304 between the first (control 1) and second (control 2) curves.
Figure 2. (A) The percent change in the diameter of the rat middle cerebral artery with increasing concentrations of UK14,304 in MCAs with flow (100 micro liter/min) and without flow (diameter 239+/-13 micro meter, n = 8 middle cerebral arteries). The transmural pressure was maintained at 85 mmHg in all middle cerebral arteries. There was no significant difference in the dilation produced by UK14,304 in middle cerebral arteries with flow or without flow. (B) The percent change in diameter for two consecutive UK14,304 dose-response curves (diameter 233 +/-8 micro meter, n = 6 middle cerebral arteries). There was no significant difference in the dilation produced by UK14,304 between the first (control 1) and second (control 2) curves.
×
(Figure 2)(B) shows the mean changes for two consecutive UK14,304 dose-response curves conducted on six MCAs. This study demonstrated that repeated dose-response curves could be conducted on a single MCA without having the response change from the first to second curve. Consequently, in the remaining studies, except where noted, we compared the second dose-response curve (experimental condition) to the first curve, which served as a control. Throughout the remaining studies, time controls were conducted at intervals to ensure that this relationship between the first and second curves remained constant.
(Figure 3) shows the results of studies that determined the receptor type stimulated by the agonist, UK14,304. Prazosin (10 sup -6 M), a selective alpha1antagonist, was without effect (n = 6 MCAs, Figure 3(A)) while phentolamine (10 sup -6 M), a nonselective alpha antagonist, completely abolished the dilation produced by the abluminal application of UK14,304 (n = 8 MCAs, Figure 3(B)). Idazoxan (10 sup -6 M), a selective alpha2antagonist, significantly attenuated the dilation (n = 7 MCAs, Figure 3(C)). Rauwolscine, a selective alpha2antagonist, abolished the dilation at a concentration of 10 sup -5 M (n = 5 MCAs, Figure 3(D)), but at a concentration of 10 sup -6 M (n = 6 MCAs) only affected the dilations at the greatest UK14,304 concentrations (data not shown). Addition of idazoxan produced a 7% decrease in the resting diameter of the MCAs (P = 0.02); no other antagonist had an effect.
Figure 3. The effects of (A) 10 sup -6 M prazosin, a selective alpha1-antagonist (diameter 262+/-14 micro meter, n = 6 middle cerebral arteries); (B) 10 sup -6 M phentolamine, a nonselective alpha-antagonist (diameter 251+/-13 micro meter, n = 8 middle cerebral arteries); (C) 10 sup -6 M idazoxan, a selective alpha2-antagonist (241+/-7 micro meter, n = 7 middle cerebral arteries); and (D) 10 sup -5 M rauwolscine, a selective alpha2-antagonist (diameter 240+/-4 micro meter, n = 5 middle cerebral arteries), on the dilations of rat middle cerebral arteries produced by UK14,304 *P < 0.05 compared to control.
Figure 3. The effects of (A) 10 sup -6 M prazosin, a selective alpha1-antagonist (diameter 262+/-14 micro meter, n = 6 middle cerebral arteries); (B) 10 sup -6 M phentolamine, a nonselective alpha-antagonist (diameter 251+/-13 micro meter, n = 8 middle cerebral arteries); (C) 10 sup -6 M idazoxan, a selective alpha2-antagonist (241+/-7 micro meter, n = 7 middle cerebral arteries); and (D) 10 sup -5 M rauwolscine, a selective alpha2-antagonist (diameter 240+/-4 micro meter, n = 5 middle cerebral arteries), on the dilations of rat middle cerebral arteries produced by UK14,304 *P < 0.05 compared to control.
Figure 3. The effects of (A) 10 sup -6 M prazosin, a selective alpha1-antagonist (diameter 262+/-14 micro meter, n = 6 middle cerebral arteries); (B) 10 sup -6 M phentolamine, a nonselective alpha-antagonist (diameter 251+/-13 micro meter, n = 8 middle cerebral arteries); (C) 10 sup -6 M idazoxan, a selective alpha2-antagonist (241+/-7 micro meter, n = 7 middle cerebral arteries); and (D) 10 sup -5 M rauwolscine, a selective alpha2-antagonist (diameter 240+/-4 micro meter, n = 5 middle cerebral arteries), on the dilations of rat middle cerebral arteries produced by UK14,304 *P < 0.05 compared to control.
×
(Figure 4) shows the response to UK14,304 in control MCAs and in MCAs after the endothelium was removed by forcing air through the lumen of the vessels. [22] Integrity of the endothelium was evaluated with acetylcholine (10 sup -5 M), which produced a dilation of 24+/-5% (n = 5). After removal of the endothelium, the dilation elicited by acetylcholine and UK14,304 was abolished (n = 7 MCAs).
Figure 4. The response to UK14,304 in control middle cerebral arteries and in middle cerebral arteries after the endothelium was removed by forcing 8 ml of air through the lumen of the vessels. The resting diameters were 254+/-6 micro meter and 212+/-16 micro meter (n = 7) for middle cerebral arteries with and without endothelium, respectively. *P < 0.05 compared to control.
Figure 4. The response to UK14,304 in control middle cerebral arteries and in middle cerebral arteries after the endothelium was removed by forcing 8 ml of air through the lumen of the vessels. The resting diameters were 254+/-6 micro meter and 212+/-16 micro meter (n = 7) for middle cerebral arteries with and without endothelium, respectively. *P < 0.05 compared to control.
Figure 4. The response to UK14,304 in control middle cerebral arteries and in middle cerebral arteries after the endothelium was removed by forcing 8 ml of air through the lumen of the vessels. The resting diameters were 254+/-6 micro meter and 212+/-16 micro meter (n = 7) for middle cerebral arteries with and without endothelium, respectively. *P < 0.05 compared to control.
×
Inhibition of nitric oxide synthase with 10 sup -5 M L-NAME completely abolished any dilation produced by UK14,304 (Figure 5). The inhibition was reversed with the addition of 10 sup -3 M L-arginine, the substrate for nitric oxide synthase, but not by the inactive isomer, D-arginine (10 sup -3 M). Two studies are shown in Figure 5. The first study using eight MCAs is represented by the filled symbols; the second study using eight MCAs is represented by the open symbols. For the studies using arginine, the concentration-response curves were conducted in the presence of L-NAME in four randomly selected MCAs using 10 sup -3 M L-arginine followed by 10 sup -3 M D-arginine. In the remaining MCAs, D-arginine curves in the presence of L-NAME were obtained first followed by L-arginine. The responses to the arginine isomers were independent of the order in which the curve was obtained; i.e., the response of the MCAs to UK14,304 in the presence of L-NAME and L-arginine was independent of whether the concentration-response curve was obtained before or after the curve with D-arginine. The same held true for D-arginine. Therefore, the data were combined for all L-arginine curves and combined for all D-arginine curves.
Figure 5. The effects of 10 sup -5 M N-nitro-L-arginine methyl ester (L-NAME), a nitric oxide synthase inhibitor, on the dilation produced by UK14,304. The open symbols show the effects of L-NAME plus 10 sup -3 M L-arginine (L-arg), the substrate for nitric oxide synthase; or L-NAME plus 10 sup -3 M D-arginine (D-arg), the inactive isomer of L-arg, on the dilation produced by UK14,304. The closed symbols represent eight middle cerebral arteries and the open symbols represent eight middle cerebral arteries where two concentration-response curves were obtained for each middle cerebral artery. Diameters of the middle cerebral arteries: control 250+/-4 micro meter; after L-NAME 220+/-8 micro meter (P < 0.05 compared to control); after L-NAME + L-arg 245+/-8 micro meter; after L-NAME + D-arg 229+/-5 micro meter (P < 0.05 compared to L-NAME + L-arg). *P < 0.05 compared to control; #P < 0.05 compared to the L-NAME + L-arg group.
Figure 5. The effects of 10 sup -5 M N-nitro-L-arginine methyl ester (L-NAME), a nitric oxide synthase inhibitor, on the dilation produced by UK14,304. The open symbols show the effects of L-NAME plus 10 sup -3 M L-arginine (L-arg), the substrate for nitric oxide synthase; or L-NAME plus 10 sup -3 M D-arginine (D-arg), the inactive isomer of L-arg, on the dilation produced by UK14,304. The closed symbols represent eight middle cerebral arteries and the open symbols represent eight middle cerebral arteries where two concentration-response curves were obtained for each middle cerebral artery. Diameters of the middle cerebral arteries: control 250+/-4 micro meter; after L-NAME 220+/-8 micro meter (P < 0.05 compared to control); after L-NAME + L-arg 245+/-8 micro meter; after L-NAME + D-arg 229+/-5 micro meter (P < 0.05 compared to L-NAME + L-arg). *P < 0.05 compared to control; #P < 0.05 compared to the L-NAME + L-arg group.
Figure 5. The effects of 10 sup -5 M N-nitro-L-arginine methyl ester (L-NAME), a nitric oxide synthase inhibitor, on the dilation produced by UK14,304. The open symbols show the effects of L-NAME plus 10 sup -3 M L-arginine (L-arg), the substrate for nitric oxide synthase; or L-NAME plus 10 sup -3 M D-arginine (D-arg), the inactive isomer of L-arg, on the dilation produced by UK14,304. The closed symbols represent eight middle cerebral arteries and the open symbols represent eight middle cerebral arteries where two concentration-response curves were obtained for each middle cerebral artery. Diameters of the middle cerebral arteries: control 250+/-4 micro meter; after L-NAME 220+/-8 micro meter (P < 0.05 compared to control); after L-NAME + L-arg 245+/-8 micro meter; after L-NAME + D-arg 229+/-5 micro meter (P < 0.05 compared to L-NAME + L-arg). *P < 0.05 compared to control; #P < 0.05 compared to the L-NAME + L-arg group.
×
Pertussis toxin (100 ng/ml) completely abolished the dilation produced by UK14,304 (Figure 6, n = 6 MCAs). For this study we show the time controls (open symbols), because 2 h elapsed between the control curve and the curve in the presence of pertussis toxin.
Figure 6. The effects of pertussis toxin (100 ng/ml for 2 h) on the dilation produced by UK14,304. The closed symbols represent six middle cerebral arteries and the open symbols represent six middle cerebral arteries where two concentration response curves were obtained for each middle cerebral artery. Time controls (control 1 and time control) are included in this figure because 2 h elapsed between the control 1 curve and the curve in the presence of pertussis toxin. Diameters of middle cerebral arteries control 1 238+/-13 micro meter; time control 232+/-17 micro meter; control 2 239+/-12 micro meter; pertussis toxin 245+/-17 micro meter. *P < 0.05 compared to control 2.
Figure 6. The effects of pertussis toxin (100 ng/ml for 2 h) on the dilation produced by UK14,304. The closed symbols represent six middle cerebral arteries and the open symbols represent six middle cerebral arteries where two concentration response curves were obtained for each middle cerebral artery. Time controls (control 1 and time control) are included in this figure because 2 h elapsed between the control 1 curve and the curve in the presence of pertussis toxin. Diameters of middle cerebral arteries control 1 238+/-13 micro meter; time control 232+/-17 micro meter; control 2 239+/-12 micro meter; pertussis toxin 245+/-17 micro meter. *P < 0.05 compared to control 2.
Figure 6. The effects of pertussis toxin (100 ng/ml for 2 h) on the dilation produced by UK14,304. The closed symbols represent six middle cerebral arteries and the open symbols represent six middle cerebral arteries where two concentration response curves were obtained for each middle cerebral artery. Time controls (control 1 and time control) are included in this figure because 2 h elapsed between the control 1 curve and the curve in the presence of pertussis toxin. Diameters of middle cerebral arteries control 1 238+/-13 micro meter; time control 232+/-17 micro meter; control 2 239+/-12 micro meter; pertussis toxin 245+/-17 micro meter. *P < 0.05 compared to control 2.
×
Because removal of the endothelium, addition of L-NAME, or addition of pertussis toxin completely blocked the UK14,304-induced dilation, it was important to determine if the vascular smooth muscle could still respond to elevations in nitric oxide in the above experimental paradigms. The response of the smooth muscle to additions of S-nitroso-N-acetylpenicillamine (10 sup -4 M), an exogenous nitric oxide donor, was not altered by the experimental perturbations (Figure 7).
Figure 7. The effects of removal of endothelium (denuded, n = 6), or with the administration of L-NAME (n = 7) and pertussis toxin (n = 6) on the dilations produced by 10 sup -4 M S-nitroso-N-acetylpenicillamine, an exogenous nitric oxide donor.
Figure 7. The effects of removal of endothelium (denuded, n = 6), or with the administration of L-NAME (n = 7) and pertussis toxin (n = 6) on the dilations produced by 10 sup -4 M S-nitroso-N-acetylpenicillamine, an exogenous nitric oxide donor.
Figure 7. The effects of removal of endothelium (denuded, n = 6), or with the administration of L-NAME (n = 7) and pertussis toxin (n = 6) on the dilations produced by 10 sup -4 M S-nitroso-N-acetylpenicillamine, an exogenous nitric oxide donor.
×
Discussion
We report four new findings regarding alpha2adrenoceptors and cerebral arteries. The first finding involves an observation: (1) stimulation of alpha2adrenoceptors on preconstricted rat middle cerebral arteries produced a dilation. The next three findings involve aspects of the mechanism of dilation: (2) the dilation required intact endothelium, (3) the dilation involved nitric oxide, and (4) a pertussis toxin-sensitive G protein was part of the signal transduction process.
In rat MCAs preconstricted with serotonin, the addition of UK14,304 to the extraluminal bath produced a dose-dependent dilation that was not influenced by the absence or presence of flow through the lumen (100 micro liter/min; Figure 2(A)). The importance of conducting the dose-response curve during the different flow states involves shear forces produced by the flow of the PSS through the lumen of the vessel. Changes in shear stress produced by luminal flow affects the contractile state of arteries by endothelial and nonendothelial mechanisms. [23] Changes in the contractile state could alter the dilations produced by stimulation of various receptor systems; however, in the case of alpha2adrenoceptors, flow (and thus shear stress) did not appear to alter the dose-dependent dilation.
Pharmacologic studies reveal that the UK14,304-mediated dilations were elicited by stimulation of alpha2adrenoceptors (Figure 3). We can rule out the involvement of alpha1adrenoceptors because the dilations produced by UK14,304 were not affected by prazosin, a selective alpha1antagonist (Figure 3(A)), and were respectively blocked and attenuated by rauwolscine (Figure 3(D)) and idazoxan (Figure 3(C)), selective alpha2antagonists. Although UK14,304 is a selective alpha2agonist, it does have imidazoline binding properties and could possibly dilate the MCAs through an imidazoline receptor. [24,25] The dilations produced by UK14,304 were blocked by phentolamine, a nonselective alpha-antagonist, and by idazoxan; both of these compounds also can antagonize imidazoline receptors. However, the involvement of imidazoline receptors can be ruled out because the dilations were completely blocked by rauwolscine, a selective alpha2antagonist without imidazoline effects. [26] Furthermore, the selective imidazoline agonist, moxonidine, [25] and the proposed endogenous imidazoline agonist, agmatine, [27] both produced a small contraction in the rat MCA; no dilations were observed (unpublished). Taken together, the results of our pharmacologic studies indicate that the vasodilatory agonist, UK14,304, stimulated alpha2adrenoceptors.
Dilations mediated by alpha2adrenoceptors have been reported for canine and porcine coronary arteries and canine femoral arteries. [8-11] Conversely, cerebral arteries from dogs and cats constrict when exposed to norepinephrine apparently through alpha2adrenoceptors. [7] Comparisons of various studies of cerebrovascular effects of alpha2adrenoceptor stimulation are complicated by the different species used, [7] different pharmacologic agents, which may have slightly different actions, and the different vessels used.
The in vivo administration of the alpha2adrenoceptor agonist, dexmedetomidine, at doses that reduced the anesthetic requirement, decreased cerebral blood flow in dogs anesthetized with either isoflurane or halothane. [3-5] In pentobarbital-anesthetized cats, clonidine, a less specific and less potent alpha2adrenoceptor agonist, decreased cerebral blood flow when measured with the tracer133Xenon, but had no effect when the tracer85Krypton was used. [6] In two of these studies, cerebral blood flow decreased in spite of an increase in mean arterial blood pressure after administration of dexmedetomidine [4,5] whereas in the other two studies blood pressure was unchanged after administration of the dexmedetomidine [3] or clonidine. [6] In the human, clonidine decreased cerebral blood flow. [28,29] Although mean arterial blood pressure decreased in these latter studies, the calculated resistance was reported to increase. The reduction in cerebral blood flow produced by the administration of alpha2adrenoceptor agonists could be due, at least in part, to neural mechanisms secondary to altered activity of the locus ceruleus or the sympathetic nervous system. [6,30] Thus, the change in cerebral blood flow may be more complicated than simply a direct effect on arteries. Furthermore, the above studies used different agonists than that used in the current study, which may have different pharmacologic actions.
Our results support the idea that alpha2agonists dilate rat middle cerebral arteries. The dilation requires intact endothelium and appears to involve nitric oxide. These conclusions are based on the results showing that removal of the endothelium and inhibition of nitric oxide synthase with L-NAME abolished the dilation to UK14,304 (Figure 4and Figure 5). After the inhibition of nitric oxide synthase with L-NAME, the response could be restored by the addition of L-arginine, the precursor for the enzyme nitric oxide synthase, but not the inactive isomer, D-arginine (Figure 5). This reversal of the inhibition provides evidence that L-NAME is acting specifically on a pathway involving L-arginine further implicating nitric oxide as a key factor in the dilation produced by UK14,304.
Our data indicate that pertussis toxin abolished the dilation to UK14,304. Pertussis toxin inactivates specific G proteins by adenosine diphosphate ribosylation of the alpha-subunit of the protein. [31] Pertussis toxin is known to inactivate several classes of G proteins including the Gi and Go. [31] The Go protein is the primary G protein found in the brain but is present in limited amounts outside the central nervous system. [32] It is not known if the Go protein is found in cerebral vessels. However, a well-accepted fact is that alpha2adrenoceptors are coupled to the Gi protein. [31,33] Little is known about the link between Gi protein activation and the resulting relaxation other than it is a key element in the alpha2adrenoceptor-mediated dilations. [11] Further studies will be needed to elucidate the G protein role in alpha2adrenoceptor dilations.
We had originally thought that the dilations mediated by UK14,304 conformed to the "classical model" where the alpha2adrenoceptors were located on the endothelium (see [21]). When stimulated, these alpha2adrenoceptors would activate nitric oxide synthase to synthesize nitric oxide. The nitric oxide formed in the endothelium would diffuse to the vascular smooth muscle and stimulate the synthesis of cyclic 3',5' guanosine monophosphate by activating soluble guanylate cyclase. Cyclic 3',5' guanosine monophosphate would produce the relaxation of the vascular smooth muscle through a number of different processes. In recent studies, [21] we provided evidence that dilations produced by alpha2adrenoceptor stimulation likely works through another mechanism that we have termed the "permissive model." In this model, the basal release of nitric oxide, which occurs even in nonstimulated conditions, permits the vasodilation to occur. Abolishing the basal release of nitric oxide by either removing the endothelium or inhibiting its synthesis with L-NAME would inhibit the vasodilation. The alpha2adrenoceptors appear to be located on the vascular smooth muscle and the direct activation of the receptor by UK14,304 produce the relaxation. In this later model, nitric oxide acts only in a permissive or modulatory role and is not the active vasodilator. [21] .
We have shown that stimulating alpha2adrenoceptors in the rat MCA with UK14,304 produced a dose-dependent dilation. This dilation required intact endothelium and involved nitric oxide and a pertussis toxin-sensitive G protein. Whether cerebral arteries in the human have a similar alpha2adrenoceptor-mediated dilatory response will have to be determined.
REFERENCES
Maze M, Tranquilli W: Alpha-2 adrenoceptor agonists: Defining the role in clinical anesthesia. ANESTHESIOLOGY 1991; 74:581-605.
Coughlan MG, Lee JG, Bosnjak ZJ, Schmeling WT, Kampine JP, Warltier DC: Direct coronary and cerebral vascular responses to dexmedetomidine. ANESTHESIOLOGY 1992; 77:998-1006.
Karlsson BR, Forsman M, Roald OK, Heier MS, Steen PA: Effect of dexmedetomidine, a selective and potent alpha sub 2 -agonist, on cerebral blood flow and oxygen consumption during halothane anesthesia in dogs. Anesth Analg 1990; 71:125-9.
Zornow MH, Fleischer JE, Scheller MS, Nakakimura K, Drummond JC: Dexmedetomidine, an alpha sub 2 -adrenergic agonist, decreases cerebral blood flow in the isoflurane-anesthetized dog. Anesth Analg 1990; 70:624-30.
McPherson RW, Kirsch JR, Traystman RJ: Inhibition of nitric oxide synthase does not affect alpha sub 2 -adrenergic-mediated cerebral vasoconstriction. Anesth Analg 1994; 78:67-72.
Kanawaiti IS, Yaksh TL, Anderson RE, Marsh RW: Effect of clonidine on cerebral blood flow and the response to arterial CO sub 2. J Cereb Blood Flow Metab 1986; 6:358-65.
Edvinsson L, Mackenzie ET, McCulloch J: Cerebral Blood Flow and Metabolism. New York, Raven, 1993, pp 183-230.
Cocks TM, Angus JA: Endothelium-dependent relaxation of coronary arteries by noradrenaline and serotonin. Nature 1983; 305:627-30.
Angus JA, Cocks TM, Satoh K: The alpha adrenoceptors on endothelial cells. Fed Proc 1986; 45:2355-9.
Miller VM, Flavahan NA, Vanhoutte PM: Pertussis toxin reduces endothelium-dependent and independent responses to alpha-2 adrenergic stimulation in systemic canine arteries and veins. J Pharmacol Exp Ther 1991; 257:290-3.
Flavahan NA, Flavahan A, Shimokawa H, Vanhoutte PM: Pertussis toxin inhibits endothelium-dependent relaxations to certain agonists in porcine coronary arteries. J Physiol (Lond) 1989; 408:549-60.
Matsuda H, Kuon E, Holtz J, Busse R: Endothelium-mediated dilations contribute to the polarity of the arterial wall in vasomotion induced by alpha-2 adrenergic agonists. J Cardiovasc Pharmacol 1985; 7:680-8.
Vinet R, Brieva C, Pinardi G, Penna M: Modulation of a-adrenergic-induced contractions by endothelium-derived relaxing factor in rat aorta. Gen Pharmacol 1991; 22:137-42.
Halpern W, Kelley M: In vitro methodology for resistance arteries. Blood Vessels 1991; 28:245-51.
Osol G, Laher I, Cipolla M: Protein kinase C modulates basal myogenic tone in resistance arteries from the cerebral circulation. Circ Res 1991; 68:359-67.
Vanhoutte PM, Miller VM: Alpha sub 2 -adrenoceptors and endothelium-derived relaxing factor. Am J Med 1989; 87:1S-5S.
Bockman CS, Jeffries WB, Abel PW: Binding and functional characterization of alpha-2 adrenergic receptor subtypes on pig vascular endothelium. J Pharmacol Exp Ther 1993; 267:1126-33.
Liao JK, Homcy CJ: The release of endothelium-derived relaxing factor via alpha sub 2 -adrenergic receptor activation is specifically mediated by G sub ia2. J Biol Chem 1993; 268:19528-33.
Ruffolo RR, Nichols AJ, Stadel JM, Hieble JP: Pharmacologic and therapeutic applications of alpha sub 2 -adrenoceptor subtypes. Annu Rev Pharmacol Toxicol 1993; 32:243-79.
Ernsberger P, Westbrooks KL, Christen MO, Schafer SG: A second generation of centrally acting antihypertensive agents act on putative I sub 1 -imidazoline receptors. J Cardiovasc Pharmacol 1992; 20:S1-10.
Bryan RM, Jr, Steenberg ML, Eichler MY, Johnson TD, Swafford MWG, Suresh MS: Permissive role of NO in alpha sub 2 -adrenoceptor-mediated dilations in rat cerebral arteries. Am J Physiol Heart Circ Physiol 1995; 269:H1171-74.
Fredricks KT, Liu Y, Rusch NJ, Lombard JH: Role of endothelium and arterial Potassium sup + channels in mediating hypoxic dilation of middle cerebral arteries. Am J Physiol Heart Circ Physiol 1994; 267:H580-6.
Bevan JA, Henrion D: Pharmacological implications of the flow-dependence of vascular smooth muscle tone. Annu Rev Pharmacol Toxicol 1994; 34:173-90.
Dominiak P: Historic aspects in the identification of the I sub 1 receptor and the pharmacology of imidazolines. Cardiovasc Drugs Ther 1994; 8:21-6.
Ernsberger P, Haxhiu MA, Graff LM, Collins LA, Dreshaj I, Grove DL, Graves ME, Schafer SG, Christen MO: A novel mechanism of action for hypertension control: Moxonidine as a selective I sub 1 -imidazoline agonist. Cardiovasc Drugs Ther 1994; 1(suppl 8):27-41.
Hieble JP, Ruffolo RR: Imidazoline receptors: Historical perspective. Fundam Clin Pharmacol 1992; 6:7s-13s.
Li G, Regunathan S, Barrow CJ, Eshraghi J, Cooper R, Reis DJ: Agmatine: An endogenous clonidine-displacing substance in the brain. Science 1994; 263:966-9.
Bertel O, Conen D, Radu EW, Muller J, Lang C, Dubach UC: Nifedipine in hypertensive emergencies. Br Med J 1983; 286:19-21.
James IM, Larbi E, Zaimis E: The effect of acute intravenous administration of clonidine (ST155) on cerebral blood flow in man. Br J Pharmacol 1970; 39:198P-9P.
Edvinsson L, Mackenzie ET, Robert J, Young AR: Cerebrovascular response to haemorrhagic hypotension in anaesthetized cats. Effects of alpha adrenoceptor antagonists. Acta Physiol Scand 1985; 123:317-23.
Yost CS: G proteins: Basic characteristics and clinical potential for the practice of anesthesia. Anesth Analg 1993; 77:822-34.
Asano T, Sembra R, Kamiya N: G sub o, a GTP-binding protein: Immunochemical and immunohistochemical localization in the rat. J Neurochem 1988; 50:1164-9.
Ruffolo RR, Nichols AJ, Stadel JM, Hieble JP: Structure and function of alpha adrenoceptors. Pharmacol Rev 1991; 43:475-505.
Figure 1. A diagram of the arteriograph for mounting middle cerebral arteries from the rat. The gauge on the tubing at right represents a flow meter for measuring perfusion of physiologic saline through the lumen of the artery; the two remaining gauges on either side of the artery represent pressure transducers for measuring the perfusion pressure across the micropipets and the middle cerebral artery. Transmural pressure could be set by raising the two reservoirs to a height above the middle cerebral artery. Luminal perfusion could be adjusted independently of the transmural pressure by providing a perfusion pressure (Delta P).
Figure 1. A diagram of the arteriograph for mounting middle cerebral arteries from the rat. The gauge on the tubing at right represents a flow meter for measuring perfusion of physiologic saline through the lumen of the artery; the two remaining gauges on either side of the artery represent pressure transducers for measuring the perfusion pressure across the micropipets and the middle cerebral artery. Transmural pressure could be set by raising the two reservoirs to a height above the middle cerebral artery. Luminal perfusion could be adjusted independently of the transmural pressure by providing a perfusion pressure (Delta P).
Figure 1. A diagram of the arteriograph for mounting middle cerebral arteries from the rat. The gauge on the tubing at right represents a flow meter for measuring perfusion of physiologic saline through the lumen of the artery; the two remaining gauges on either side of the artery represent pressure transducers for measuring the perfusion pressure across the micropipets and the middle cerebral artery. Transmural pressure could be set by raising the two reservoirs to a height above the middle cerebral artery. Luminal perfusion could be adjusted independently of the transmural pressure by providing a perfusion pressure (Delta P).
×
Figure 2. (A) The percent change in the diameter of the rat middle cerebral artery with increasing concentrations of UK14,304 in MCAs with flow (100 micro liter/min) and without flow (diameter 239+/-13 micro meter, n = 8 middle cerebral arteries). The transmural pressure was maintained at 85 mmHg in all middle cerebral arteries. There was no significant difference in the dilation produced by UK14,304 in middle cerebral arteries with flow or without flow. (B) The percent change in diameter for two consecutive UK14,304 dose-response curves (diameter 233 +/-8 micro meter, n = 6 middle cerebral arteries). There was no significant difference in the dilation produced by UK14,304 between the first (control 1) and second (control 2) curves.
Figure 2. (A) The percent change in the diameter of the rat middle cerebral artery with increasing concentrations of UK14,304 in MCAs with flow (100 micro liter/min) and without flow (diameter 239+/-13 micro meter, n = 8 middle cerebral arteries). The transmural pressure was maintained at 85 mmHg in all middle cerebral arteries. There was no significant difference in the dilation produced by UK14,304 in middle cerebral arteries with flow or without flow. (B) The percent change in diameter for two consecutive UK14,304 dose-response curves (diameter 233 +/-8 micro meter, n = 6 middle cerebral arteries). There was no significant difference in the dilation produced by UK14,304 between the first (control 1) and second (control 2) curves.
Figure 2. (A) The percent change in the diameter of the rat middle cerebral artery with increasing concentrations of UK14,304 in MCAs with flow (100 micro liter/min) and without flow (diameter 239+/-13 micro meter, n = 8 middle cerebral arteries). The transmural pressure was maintained at 85 mmHg in all middle cerebral arteries. There was no significant difference in the dilation produced by UK14,304 in middle cerebral arteries with flow or without flow. (B) The percent change in diameter for two consecutive UK14,304 dose-response curves (diameter 233 +/-8 micro meter, n = 6 middle cerebral arteries). There was no significant difference in the dilation produced by UK14,304 between the first (control 1) and second (control 2) curves.
×
Figure 3. The effects of (A) 10 sup -6 M prazosin, a selective alpha1-antagonist (diameter 262+/-14 micro meter, n = 6 middle cerebral arteries); (B) 10 sup -6 M phentolamine, a nonselective alpha-antagonist (diameter 251+/-13 micro meter, n = 8 middle cerebral arteries); (C) 10 sup -6 M idazoxan, a selective alpha2-antagonist (241+/-7 micro meter, n = 7 middle cerebral arteries); and (D) 10 sup -5 M rauwolscine, a selective alpha2-antagonist (diameter 240+/-4 micro meter, n = 5 middle cerebral arteries), on the dilations of rat middle cerebral arteries produced by UK14,304 *P < 0.05 compared to control.
Figure 3. The effects of (A) 10 sup -6 M prazosin, a selective alpha1-antagonist (diameter 262+/-14 micro meter, n = 6 middle cerebral arteries); (B) 10 sup -6 M phentolamine, a nonselective alpha-antagonist (diameter 251+/-13 micro meter, n = 8 middle cerebral arteries); (C) 10 sup -6 M idazoxan, a selective alpha2-antagonist (241+/-7 micro meter, n = 7 middle cerebral arteries); and (D) 10 sup -5 M rauwolscine, a selective alpha2-antagonist (diameter 240+/-4 micro meter, n = 5 middle cerebral arteries), on the dilations of rat middle cerebral arteries produced by UK14,304 *P < 0.05 compared to control.
Figure 3. The effects of (A) 10 sup -6 M prazosin, a selective alpha1-antagonist (diameter 262+/-14 micro meter, n = 6 middle cerebral arteries); (B) 10 sup -6 M phentolamine, a nonselective alpha-antagonist (diameter 251+/-13 micro meter, n = 8 middle cerebral arteries); (C) 10 sup -6 M idazoxan, a selective alpha2-antagonist (241+/-7 micro meter, n = 7 middle cerebral arteries); and (D) 10 sup -5 M rauwolscine, a selective alpha2-antagonist (diameter 240+/-4 micro meter, n = 5 middle cerebral arteries), on the dilations of rat middle cerebral arteries produced by UK14,304 *P < 0.05 compared to control.
×
Figure 4. The response to UK14,304 in control middle cerebral arteries and in middle cerebral arteries after the endothelium was removed by forcing 8 ml of air through the lumen of the vessels. The resting diameters were 254+/-6 micro meter and 212+/-16 micro meter (n = 7) for middle cerebral arteries with and without endothelium, respectively. *P < 0.05 compared to control.
Figure 4. The response to UK14,304 in control middle cerebral arteries and in middle cerebral arteries after the endothelium was removed by forcing 8 ml of air through the lumen of the vessels. The resting diameters were 254+/-6 micro meter and 212+/-16 micro meter (n = 7) for middle cerebral arteries with and without endothelium, respectively. *P < 0.05 compared to control.
Figure 4. The response to UK14,304 in control middle cerebral arteries and in middle cerebral arteries after the endothelium was removed by forcing 8 ml of air through the lumen of the vessels. The resting diameters were 254+/-6 micro meter and 212+/-16 micro meter (n = 7) for middle cerebral arteries with and without endothelium, respectively. *P < 0.05 compared to control.
×
Figure 5. The effects of 10 sup -5 M N-nitro-L-arginine methyl ester (L-NAME), a nitric oxide synthase inhibitor, on the dilation produced by UK14,304. The open symbols show the effects of L-NAME plus 10 sup -3 M L-arginine (L-arg), the substrate for nitric oxide synthase; or L-NAME plus 10 sup -3 M D-arginine (D-arg), the inactive isomer of L-arg, on the dilation produced by UK14,304. The closed symbols represent eight middle cerebral arteries and the open symbols represent eight middle cerebral arteries where two concentration-response curves were obtained for each middle cerebral artery. Diameters of the middle cerebral arteries: control 250+/-4 micro meter; after L-NAME 220+/-8 micro meter (P < 0.05 compared to control); after L-NAME + L-arg 245+/-8 micro meter; after L-NAME + D-arg 229+/-5 micro meter (P < 0.05 compared to L-NAME + L-arg). *P < 0.05 compared to control; #P < 0.05 compared to the L-NAME + L-arg group.
Figure 5. The effects of 10 sup -5 M N-nitro-L-arginine methyl ester (L-NAME), a nitric oxide synthase inhibitor, on the dilation produced by UK14,304. The open symbols show the effects of L-NAME plus 10 sup -3 M L-arginine (L-arg), the substrate for nitric oxide synthase; or L-NAME plus 10 sup -3 M D-arginine (D-arg), the inactive isomer of L-arg, on the dilation produced by UK14,304. The closed symbols represent eight middle cerebral arteries and the open symbols represent eight middle cerebral arteries where two concentration-response curves were obtained for each middle cerebral artery. Diameters of the middle cerebral arteries: control 250+/-4 micro meter; after L-NAME 220+/-8 micro meter (P < 0.05 compared to control); after L-NAME + L-arg 245+/-8 micro meter; after L-NAME + D-arg 229+/-5 micro meter (P < 0.05 compared to L-NAME + L-arg). *P < 0.05 compared to control; #P < 0.05 compared to the L-NAME + L-arg group.
Figure 5. The effects of 10 sup -5 M N-nitro-L-arginine methyl ester (L-NAME), a nitric oxide synthase inhibitor, on the dilation produced by UK14,304. The open symbols show the effects of L-NAME plus 10 sup -3 M L-arginine (L-arg), the substrate for nitric oxide synthase; or L-NAME plus 10 sup -3 M D-arginine (D-arg), the inactive isomer of L-arg, on the dilation produced by UK14,304. The closed symbols represent eight middle cerebral arteries and the open symbols represent eight middle cerebral arteries where two concentration-response curves were obtained for each middle cerebral artery. Diameters of the middle cerebral arteries: control 250+/-4 micro meter; after L-NAME 220+/-8 micro meter (P < 0.05 compared to control); after L-NAME + L-arg 245+/-8 micro meter; after L-NAME + D-arg 229+/-5 micro meter (P < 0.05 compared to L-NAME + L-arg). *P < 0.05 compared to control; #P < 0.05 compared to the L-NAME + L-arg group.
×
Figure 6. The effects of pertussis toxin (100 ng/ml for 2 h) on the dilation produced by UK14,304. The closed symbols represent six middle cerebral arteries and the open symbols represent six middle cerebral arteries where two concentration response curves were obtained for each middle cerebral artery. Time controls (control 1 and time control) are included in this figure because 2 h elapsed between the control 1 curve and the curve in the presence of pertussis toxin. Diameters of middle cerebral arteries control 1 238+/-13 micro meter; time control 232+/-17 micro meter; control 2 239+/-12 micro meter; pertussis toxin 245+/-17 micro meter. *P < 0.05 compared to control 2.
Figure 6. The effects of pertussis toxin (100 ng/ml for 2 h) on the dilation produced by UK14,304. The closed symbols represent six middle cerebral arteries and the open symbols represent six middle cerebral arteries where two concentration response curves were obtained for each middle cerebral artery. Time controls (control 1 and time control) are included in this figure because 2 h elapsed between the control 1 curve and the curve in the presence of pertussis toxin. Diameters of middle cerebral arteries control 1 238+/-13 micro meter; time control 232+/-17 micro meter; control 2 239+/-12 micro meter; pertussis toxin 245+/-17 micro meter. *P < 0.05 compared to control 2.
Figure 6. The effects of pertussis toxin (100 ng/ml for 2 h) on the dilation produced by UK14,304. The closed symbols represent six middle cerebral arteries and the open symbols represent six middle cerebral arteries where two concentration response curves were obtained for each middle cerebral artery. Time controls (control 1 and time control) are included in this figure because 2 h elapsed between the control 1 curve and the curve in the presence of pertussis toxin. Diameters of middle cerebral arteries control 1 238+/-13 micro meter; time control 232+/-17 micro meter; control 2 239+/-12 micro meter; pertussis toxin 245+/-17 micro meter. *P < 0.05 compared to control 2.
×
Figure 7. The effects of removal of endothelium (denuded, n = 6), or with the administration of L-NAME (n = 7) and pertussis toxin (n = 6) on the dilations produced by 10 sup -4 M S-nitroso-N-acetylpenicillamine, an exogenous nitric oxide donor.
Figure 7. The effects of removal of endothelium (denuded, n = 6), or with the administration of L-NAME (n = 7) and pertussis toxin (n = 6) on the dilations produced by 10 sup -4 M S-nitroso-N-acetylpenicillamine, an exogenous nitric oxide donor.
Figure 7. The effects of removal of endothelium (denuded, n = 6), or with the administration of L-NAME (n = 7) and pertussis toxin (n = 6) on the dilations produced by 10 sup -4 M S-nitroso-N-acetylpenicillamine, an exogenous nitric oxide donor.
×