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Meeting Abstracts  |   March 1996
Spinal Antinociceptive Action of an N-Type Voltage-dependent Calcium Channel Blocker and the Synergistic Interaction with Morphine
Author Notes
  • (Omote) Assistant Professor.
  • (Kawamata, Satoh) Instructor in Anesthesiology.
  • (Iwasaki) Associate Professor of Anesthesiology.
  • (Namiki) Professor and Chairman of Anesthesiology.
  • Received from the Department of Anesthesiology, Sapporo Medical University School of Medicine, Sapporo, Japan. Submitted for publication July 6, 1995. Accepted for publication November 16, 1995.
  • Address reprint requests to Dr. Omote: Department of Anesthesiology, Sapporo Medical University School of Medicine, South-1, West-16, Chuoku, Sapporo, 060 Japan. Address electronic mail to: komote@sapmed.ac.jp.
Article Information
Meeting Abstracts   |   March 1996
Spinal Antinociceptive Action of an N-Type Voltage-dependent Calcium Channel Blocker and the Synergistic Interaction with Morphine
Anesthesiology 3 1996, Vol.84, 636-643. doi:
Anesthesiology 3 1996, Vol.84, 636-643. doi:
SENSORY neurons have been shown to possess four main kinds of voltage-dependent calcium channels, termed the L-, N-, T- and P-channels, [1–3] which are distinguished on the basis of the degree of membrane depolarization needed to activate the currents (activation threshold), their inactivation characteristics, and their pharmacologic properties. Although the physiologic roles of these different types of calcium channels are not completely understood, both the L-type and N-type calcium ion channels have been implicated in the release of neurotransmitters/neuromodulators from sensory neurons in the spinal cord. [4,5] T-type channels are hypothesized to be involved in regulation of neuronal excitability and pacemaker activity. [4,6] The fourth type, the P-type channel, has been defined in the dorsal horn but the transmitter coupling at this site has not yet been determined. [3,7] .
While L-type currents exist in the dorsal horn, intrathecally administered L-type calcium channel blockers do not show any tendency to prolong the tail flick latency, indicating that the L-type calcium channel does not directly contribute to spinal nociception in acute thermal stimulation. [8] Bell [9] has reported that L-type channels play a minor role in synaptic transmission and have some function in connections between intrinsic spinal neurons. Conversely, some reports demonstrated that disruption of calcium ion movement through N-type calcium channels inhibited release of neuropeptides (substance P and calcitonin gene related peptide (CGRP)) from the dorsal half of the rat spinal cord. [10,11] Spinal localization of N-type channels was shown in the superficial lamina of the dorsal horn. [12] This explains why blockade of the spinal N-type calcium channel interferes with normal sensory processing, resulting in contribution to antinociception.
Opioids block calcium influx through the calcium channel by binding the opioid receptor in a naloxone-sensitive manner [13] to reduce the presynaptic calcium influx, resulting in suppression of neurotransmitter release from primary afferents conveying nociceptive information. [14–16] We reported that L-type voltage-dependent calcium channel blockers (verapamil, diltiazem, and nicardipine), which alone did not produce analgesia, potentiated the analgesic effects of morphine at the spinal cord. [8] This suggests an interaction between L-type voltage-dependent calcium channels and opioid receptors.
In the current study, we examined the antinociceptive effects of the N-type voltage-dependent calcium channel blocker, omega-conotoxin GVIA (omega-CgTx), using thermal and mechanical noxious stimuli. We also examined the antinociceptive interactions between morphine and omega-CgTx at the level of the spinal cord.
Materials and Methods
Experiments were conducted according to the protocol approved by the Sapporo Medical University Animal Care and Use Committee.
Animals
Male Sprague-Dawley rats (weighing 250–300 g, Japan SLC, Hamamatsu, Japan) were used. The animals were housed individually in a temperature-controlled (21+/-1 degree C) room with a 12-h light:dark cycle (lights on 7:00 AM-7:00 PM) and were allowed free access to food and water.
Surgical Preparation
Using a modification of the method described by Bahar et al., [17] chronic lumbar intrathecal catheters were implanted in rats anesthetized with halothane. Briefly, a polyethylene catheter (PE-10, Clay Adams, Parsippany, NJ) was introduced 15 mm cephalad into the lumbar subarachnoid space at the L4-L5 vertebral level with the tip of the catheter located near the lumbar enlargement of the spinal cord. The distal end of the catheter was tunnelled subcutaneously to emerge at the neck. The volume of dead space of the intrathecal catheter was 10 micro liter. After the intrathecal catheters were implanted, the rats were housed in individual cages. At least 6 days of postsurgical recovery was allowed before animals were used in experiments. In the experiments, we used only animals that showed normal behavior and motor function and that had showed complete paralysis of tail and bilateral hind legs after administration of 2% lidocaine 10 micro liter through the intrathecal catheter. After the experimentation, in which the animals were used only once, each animal was killed by an overdose of halothane. The position of the catheter tip was verified at autopsy and the spread of injected material was determined by a postmortem intrathecal injection of 1% methylene blue (10 micro liter) followed by a flush of physiologic saline.
Nociceptive Tests and Motor Function Test
The tail flick (TF) and the mechanical paw pressure (MPP) tests were used to assess thermal and mechanical nociceptive thresholds, respectively. The TF test was employed by monitoring latency to withdrawal from the heat source (a 50-W projection lamp bulb) focused on the distal segment of the tail, using a thermal analgesimeter (KN-205E, Natsume, Tokyo, Japan). The location on the stimulated tail was systemically varied so that the same portion of the tail was not exposed repeatedly to the light source. The mean baseline TF latency in the experiment was 3.4 s (3.1–3.7 s) and a cutoff time of 10.0 s was adopted to minimize damage to the skin of the tail.
The MPP test was employed on the right hind paw of the animal, using a Randall Selitto type analgesimeter (TK-201, Unicom, Tokyo, Japan). The head and body of the rat was loosely wrapped in a soft cloth and gently held in the hand of the observer. The hind paw was then placed on a flat plastic surface and pressure was applied to the unrestrained dorsal surface of the hind paw by a small conical projection with a rounded tip. The apparatus was set up to apply a force of 0–200 mmHg, increasing from zero at a rate of 15 mmHg/s to the cutoff pressure of 200 mmHg. Mechanical paw pressure threshold was defined as the pressure to withdrawal of the hind paw. The mean baseline MPP threshold in the experiment was 60 mmHg (52–72 mmHg).
Motor function before and after intrathecal drug injection was examined using the scale proposed by Langerman et al. [18] for rabbits, which we applied to the rat model as follows: 0 = free movement of hind limbs without limitation; 1 = limited or asymmetrical movement of the hind limbs to support the body and walk; 2 = inability to support the back of the body on hind limbs, with detectable ability to move the limbs and respond to pain stimulus; and 3 = total paralysis of the hind limbs.
Drug Administration
Intrathecal drug administration was accomplished by using a microinjection syringe (Hamilton, Reno, NV) connected to the intrathecal catheter in awake, briefly restrained rats. All drugs or drug combinations were administered manually over 10 s and followed by a 10-micro liter flush of sterile physiologic saline to ensure that the drug reached the spinal cord.
The drugs administered in the experiments were morphine hydrochloride (MW 375.85; Sankyo, Tokyo, Japan), omega-conotoxin GVIA (omega-CgTx, MW 3037; Research Biochemicals, Natick, MA), and naloxone hydrochloride (MW 363.84; Sankyo). Drugs were freshly dissolved in sterile physiologic saline in concentrations that allowed intrathecal injections in 10-micro liter volumes.
Behavioral Testing
Behavioral assessments were performed between 10:00 and 12:00 AM to control for diurnal fluctuations in opioid sensitivity. Before the animals were used in each experiment, we measured the baseline TF latency, MPP threshold, and motor function to confirm the neurologically normal state. After determination of baseline values, rats received intrathecal injections of morphine (1, 2, 5, or 10 micro gram), omega-CgTx (0.05, 0.1, 0.25, or 0.5 micro gram), combination of morphine and omega-CgTx, or physiologic saline as control. Tail flick latencies or MPP thresholds were determined 5, 10, 15, 20, 30, 45, and 60 min after the intrathecal administration. In the animals receiving the combination of morphine and omega-CgTx, 200 micro gram/kg naloxone was administered intraperitoneally 61 min after administration of the combined drugs, and the latencies or thresholds were again evaluated 5 min after naloxone administration. The observers were not blinded as to which agent or combination was given each time.
The responses for the TF and MPP tests were calculated as the percent maximum possible effect (postdrug value - baseline value)/(cutoff value - baseline value) x 100. Dose-responses were constructed and compared using measurements at a set time in each animal (15 min after intrathecal administration).
Isobolographic analysis of interactions was used to define the nature of the functional interaction between morphine and omega-CgTx. From the dose-response curves of morphine and omega-CgTx alone, the respective dose producing a 50% maximum possible effect (ED50value) was determined for each drug in both nociceptive tests to construct isobolographic analysis. When the morphine and omega-CgTx were coadministered, a constant dose ratio was used, based on the ED50values of each agent administered separately so that equieffective doses were given together. The equieffective dose ratio was 20:1 for morphine and omega-CgTx, respectively, in both tests. Consequently, the doses of the combination of morphine and omega-CgTx were 0.3 micro gram and 0.015 micro gram, 0.5 micro gram and 0.025 micro gram, 1 micro gram and 0.05 micro gram, or 2 micro gram and 0.1 micro gram, respectively.
Statistical Analysis
The effects of drugs on TF latency and MPP threshold were evaluated by one-way analysis of variance and Scheffe's F-test. A P value < 0.05 was considered to be statistically significant.
For evaluation of the interaction between intrathecal morphine and intrathecal omega-CgTx, isobolograms were constructed using ED50values obtained when the agents were administered separately and together. The construction of the dose-response curves and the determination of doses producing 50% maximum possible effect (ED50) as well as 95% confidence intervals were computed. The ED50values and 95% confidence intervals for omega-CgTx and morphine alone were plotted on the X and Y axes, respectively, and the theoretical additive point was calculated according to the method described by Tallarida et al. [19] From the dose-response curve of the combined drugs, the ED50value of the total dose of the combination was calculated, and based on the known dose ratio (20:1), the single doses of the agents in the combination were obtained for plotting on the isobologram. Statistical significance between the theoretical additive points and the experimentally derived ED50value was evaluated using Student's t test. An experimental ED50that was significantly less than the theoretical additive ED50(P < 0.05) was considered to indicate a synergistic interaction between morphine and omega-CgTx.
The method of total fractions was calculated to obtain the magnitude of the interaction as described by Roerig et al. [20] Total fraction values were calculated as follows:
(ED50of morphine when injected with omega-CgTx)/(ED50of morphine alone)+(ED50of omega-CgTx when injected with morphine)/(ED50of omega-CgTx alone)
Values near 1 indicate an additive interaction, values less than 1 indicate a synergistic interaction, and values greater than 1 imply an antagonistic (less than additive) interaction between intrathecal morphine and omega-CgTx.
Results
Effects of Intrathecal omega-CgTx and Morphine on Nociception
Intrathecally administered omega-CgTx alone produced a significant prolongation of TF latency and a significant increase in MPP threshold in a time- and dose-dependent manner (Figure 1and Figure 2). Peak effects of omega-CgTx were observed 15 min after intrathecal administration in both nociceptive tests. At a high dose of 0.5 micro gram omega-CgTx, most animals showed intermittent spontaneous TF and shaking behavior approximately 30–60 min after the administration, which limited the study on the measurement of TF latency at this period. However, at doses of 0.05, 0.1, and 0.25 micro gram omega-CgTx, the spontaneous TF and shaking behavior were not observed during 60 min after administration. Intrathecally administered morphine alone also showed antinociceptive effects in TF and MPP tests in a time-dependent manner (data not shown). The times to peak effects of intrathecal morphine in both tests were 15 min after the administration, which were same as the time observed to peak effects of intrathecal omega-CgTx. Figure 2shows the dose response curves for intrathecal morphine and omega-CgTx in the TF and MPP tests, which indicate that both drugs produced a dose-dependent antinociceptive effects in thermal and mechanical nociceptive tests.
Figure 1. Time course effects of intrathecally administered omega-conotoxin (omega-CgTx) in tail flick and mechanical paw pressure tests. Data are represented as mean+/-SEM from 5 or 6 rats.
Figure 1. Time course effects of intrathecally administered omega-conotoxin (omega-CgTx) in tail flick and mechanical paw pressure tests. Data are represented as mean+/-SEM from 5 or 6 rats.
Figure 1. Time course effects of intrathecally administered omega-conotoxin (omega-CgTx) in tail flick and mechanical paw pressure tests. Data are represented as mean+/-SEM from 5 or 6 rats.
×
Figure 2. Dose-response lines for morphine and omega-conotoxin in the tail flick and the mechanical paw pressure tests. The data points represent the percent maximum possible effect seen 15 min after intrathecal administration of drugs. The number of observations at each point was 5–8. Data are mean+/-SEM.
Figure 2. Dose-response lines for morphine and omega-conotoxin in the tail flick and the mechanical paw pressure tests. The data points represent the percent maximum possible effect seen 15 min after intrathecal administration of drugs. The number of observations at each point was 5–8. Data are mean+/-SEM.
Figure 2. Dose-response lines for morphine and omega-conotoxin in the tail flick and the mechanical paw pressure tests. The data points represent the percent maximum possible effect seen 15 min after intrathecal administration of drugs. The number of observations at each point was 5–8. Data are mean+/-SEM.
×
In motor function testing, the scale before omega-CgTx administration was 0 and the scale after the administration at doses employed was 0 during the observation period (data not shown).
Effects of the Combination of Intrathecal Morphine and omega-CgTx
(Figure 3) shows the effects of an intrathecal ineffective dose of morphine (2 micro gram) combined with a slightly effective dose of omega-CgTx (0.1 micro gram) in the TF and MPP tests. In contrast to the ineffectiveness of 2 micro gram morphine and slight effectiveness of 0.1 micro gram omega-CgTx, the concomitant administration of the drugs produced a significant prolongation of the TF latency and a significant increase in MPP threshold. This potentiation was immediately reversed by intraperitoneally administered naloxone 200 micro gram/kg (Figure 3). Figure 4demonstrates the effects of the combination of morphine and omega-CgTx at the dose of the 20:1 ratio. In both nociceptive tests, these combinations demonstrate a dose- and time-dependent prolongation of the latency and increase in the threshold. At the combination doses employed in the experiment, the animals did not show any spontaneous TF or shaking behavior seen in the most animals treated with 0.5 micro gram omega-CgTx. The motor function scales were all 0 before and after the administration of the combined drugs (data not shown).
Figure 3. Effects of the combination of morphine and omega-conotoxin on tail flick latency (left) and mechanical paw pressure threshold (right). When a slightly effective dose of omega-CgTx (0.1 micro gram; open circles, n = 5) was combined with 2 micro gram of morphine (filled circles, n = 7), significant prolongation of TF latency and significant elevation of MPP threshold were shown (filled squares, n = 6). The effects of the combinations were reversed by intraperitoneally administered naloxone (200 micro gram/kg). Data for omega-CgTx alone are transferred from Figure 1. Data are mean+/-SEM. *P < 0.05 compared with morphine alone and omega-CgTx alone at individual times. (dagger)P < 0.05 compared with the percent maximum possible effect value 60 min after the intrathecal administration of the combination.
Figure 3. Effects of the combination of morphine and omega-conotoxin on tail flick latency (left) and mechanical paw pressure threshold (right). When a slightly effective dose of omega-CgTx (0.1 micro gram; open circles, n = 5) was combined with 2 micro gram of morphine (filled circles, n = 7), significant prolongation of TF latency and significant elevation of MPP threshold were shown (filled squares, n = 6). The effects of the combinations were reversed by intraperitoneally administered naloxone (200 micro gram/kg). Data for omega-CgTx alone are transferred from Figure 1. Data are mean+/-SEM. *P < 0.05 compared with morphine alone and omega-CgTx alone at individual times. (dagger)P < 0.05 compared with the percent maximum possible effect value 60 min after the intrathecal administration of the combination.
Figure 3. Effects of the combination of morphine and omega-conotoxin on tail flick latency (left) and mechanical paw pressure threshold (right). When a slightly effective dose of omega-CgTx (0.1 micro gram; open circles, n = 5) was combined with 2 micro gram of morphine (filled circles, n = 7), significant prolongation of TF latency and significant elevation of MPP threshold were shown (filled squares, n = 6). The effects of the combinations were reversed by intraperitoneally administered naloxone (200 micro gram/kg). Data for omega-CgTx alone are transferred from Figure 1. Data are mean+/-SEM. *P < 0.05 compared with morphine alone and omega-CgTx alone at individual times. (dagger)P < 0.05 compared with the percent maximum possible effect value 60 min after the intrathecal administration of the combination.
×
Figure 4. Effects of the combination of morphine and omega-conotoxin at the dose of the 20:1 ratio, respectively. In tail flick and mechanical paw pressure tests, these combinations demonstrate a dose- and time-dependent prolongation of the latency and increase in the threshold, respectively. Data are mean+/-SEM.
Figure 4. Effects of the combination of morphine and omega-conotoxin at the dose of the 20:1 ratio, respectively. In tail flick and mechanical paw pressure tests, these combinations demonstrate a dose- and time-dependent prolongation of the latency and increase in the threshold, respectively. Data are mean+/-SEM.
Figure 4. Effects of the combination of morphine and omega-conotoxin at the dose of the 20:1 ratio, respectively. In tail flick and mechanical paw pressure tests, these combinations demonstrate a dose- and time-dependent prolongation of the latency and increase in the threshold, respectively. Data are mean+/-SEM.
×
Interaction between Morphine and omega-CgTx
(Table 1) shows the ED50s and 95% confidence intervals for morphine, omega-CgTx, and the combination in TF and MPP tests. As shown in Figure 5, the experimentally derived ED50and 95% confidence interval in the isobologram decreased below the theoretically additive dose line. The confidence intervals of the theoretical additive point and those of the experimental point did not overlap in the isobolograms of TF and MPP tests. These analyses revealed a significantly synergistic interaction between morphine and omega-CgTx in TF and MPP tests (P < 0.05). The total fraction values, which indicate the magnitude of the interaction, were less than 1 in both tests, indicating a synergistic interaction (Table 1).
Table 1. ED50and Total Fraction of Morphine and omega-Conotoxin in Tail Flick and Mechanical Paw Pressure Tests
Image not available
Table 1. ED50and Total Fraction of Morphine and omega-Conotoxin in Tail Flick and Mechanical Paw Pressure Tests
×
Figure 5. Isobolograms showing the interaction between morphine and omega-conotoxin in tail flick and mechanical paw pressure tests. In both isobolograms, the experimental points in both tests were observed below the theoretical additive points, indicating a synergistic interaction. Each point on the graph represent ED50values and 95% confidence intervals.
Figure 5. Isobolograms showing the interaction between morphine and omega-conotoxin in tail flick and mechanical paw pressure tests. In both isobolograms, the experimental points in both tests were observed below the theoretical additive points, indicating a synergistic interaction. Each point on the graph represent ED50values and 95% confidence intervals.
Figure 5. Isobolograms showing the interaction between morphine and omega-conotoxin in tail flick and mechanical paw pressure tests. In both isobolograms, the experimental points in both tests were observed below the theoretical additive points, indicating a synergistic interaction. Each point on the graph represent ED50values and 95% confidence intervals.
×
Discussion
The current study demonstrated that intrathecally administered omega-CgTx produced antinociceptive effects against thermal and mechanical noxious stimuli in a time- and dose-dependent manner. We also demonstrated in this study that intrathecally coadministered morphine and omega-CgTx showed a synergistic antinociceptive interaction against both noxious stimuli.
The distinction between N- and L-channels is based on their different inactivation characteristics and their different pharmacologic properties; L-channels are blocked by dihydropyridine calcium blockers, [21] and N-channels, by omega-CgTx. [21,22] Some studies on the distribution of these two channel subtypes in sensory neurons show that L-channels may not be very common in nerve terminals and may be preferentially localized in the cell body, whereas N-channels are localized in the transmitter release zone in nerve terminals. [2] Thus, the N-, rather than L-type, is believed to be the most important channel in regulatory neurotransmitter release from the nerve terminals in the central nervous system.
N-type calcium channels are selectively blocked by omega-CgTx via a competitive mechanism. [23,24] The presence of specific omega-CgTx-binding sites was shown in the dorsal half of the rat spinal cord, especially superficial lamina of the dorsal horn (I and II of Rexed). [11,12,25] Magi et al. [10] reported that omega-CgTx significantly reduced the potassium-induced release of neuropeptides (substance P and CGRP) from the dorsal half of the rat spinal cord. Santicioli et al. [11] also demonstrated that omega-CgTx, but not L-type calcium channel blocker nifedipine, abolished an outflow of CGRP-like immunoactivity, which was evoked by electrical field stimulation from perfused slices of the dorsal half of the rat spinal cord. Thus, omega-CgTx sensitive N-type calcium channel opening must be essential for the triggering of neurotransmitter release from primary afferents. Therefore, disruption of calcium ion movement through N-type calcium channels by omega-CgTx and consequent inhibition of releasing neurotransmitters should interfere with normal sensory processing, resulting in contribution to antinociception. It seems that the dose-dependent antinociceptive action of intrathecally administered omega-CgTx shown in the current study reflects the inhibiting neurotransmitter release caused by the N-type calcium channel blockade.
Other less selective N-type calcium channel blockers such as aminoglycoside antibiotics, when administered intraperitoneally, produce analgesia in rats and mice as assessed by TF, carrageenan-induced articular incapacity, and hot plate tests. [26,27] Recently, Malmberg and Yaksh [28] demonstrated that spinal injection of certain synthetic omega-conopeptides, selective blockers for N-type voltage-dependent calcium channels, produced a powerful dose-dependent suppression of the first and second phase of the formalin test, although they only produced a modest antinociceptive effect to the hot plate test. Furthermore, in the model of peripheral nerve injury, omega-conopeptides produced a dose-dependent blockade of tactile allodynia. [29] Thus, it seems clear that the N-type calcium channel is involved in facilitated nociceptive processing at the spinal level in the models in which there is a hyperalgesic component.
A previous study showed that intracerebroventricular and intraperitoneal administration of large doses of omega-CgTx caused neurologic dysfunction (e.g., paroxysmal shaking, convulsion) and motor impairment. [30] In the current study, a large dose of intrathecal omega-CgTx (0.5 micro gram) caused intermittent spontaneous TF and shaking, which limited the measurement of TF latency 30–60 min after drug administration. The mechanism of these behaviors is unknown. The peak antinociceptive effects in TF and MPP tests were observed 15 min after administration, and the behavioral effects were not apparent at this time. Thus, it is unlikely that the spontaneous TF and shaking found in rats account for the suppression of nociceptive responses. We think that the changes in motor tone do not contribute to the suppression of nociceptive responses. Conversely, in motor function testing, the scores before and after the administration of omega-CgTx, morphine, and the combination were all 0 points, indicating lack of a loss of motor tone by omega-CgTx.
The most important result obtained in this study was that intrathecal N-type calcium channel blockers synergistically potentiated the antinociception of the intrathecal morphine. To investigate the antinociceptive interaction between intrathecal morphine and omega-CgTx, isobolographic analysis was adopted in the current study. Using this analysis, the results in this experiment revealed a significant synergistic antinociceptive interaction between morphine and omega-CgTx in the TF and MPP tests. The magnitude of the interaction, e.g., total fraction values, also less than 1, indicate a synergistic interaction. Furthermore, the degrees of synergism in TF and MPP tests were comparable.
Although the mechanism of the synergism was not clear, the observed synergy in the current study suggests that morphine and omega-CgTx act, in part, at distinct and separate sites to produce antinociception. Malmberg and Yaksh [31] reported that chronic infusion of omega-conopeptides that block N-type calcium channels produced a powerful antinociception, with minimal development of tolerance. In contrast, morphine infusion, which acts through a G protein-coupled channel, developed tolerance. This emphasizes the likelihood that the N-type channel blockers act in a manner separate from an opioid receptor.
Spampinato et al. [32] found that the antinociceptive responses elicited by intracerebroventricular micro-opioid agonists were significantly prolonged and potentiated by omega-CgTx. Morphine possesses the micro- and delta-agonistic activities to produce suppression of the responses to somatic nociception. [33] The activation of micro- and delta-receptors by a variety of ligands produces an opening of potassium ion channels, not directly, but via either cyclic adenosine monophosphate and/or G protein intermediations. [34,35] The net result of this action on a neuron would be hyperpolarization and a reduction in firing. Thus, opioid action through the micro and/or delta receptor might contribute to produce synergistic antinociception.
We demonstrated previously that L-type calcium channel blockers, verapamil, diltiazem, and nicardipine, also potentiated the antinociceptive effect of morphine at the spinal level. [8] Therefore, it seems that morphine produces synergistic antinociceptive interaction with N- and L-type calcium channel blockers. However, it is extremely difficult to interpret the molecular events underlying the behavioral effects induced by drug treatment because they are the result of the complex interaction and integration of different neuronal pathways.
In conclusion, intrathecally administered omega-CgTx produced antinociception in TF and MPP tests, emphasizing the importance of N-type voltage-dependent calcium channels in the spinal cord on nociception. The synergistic antinociceptive interaction observed after coadministration of omega-CgTx and morphine is suggestive of functional interaction between N-type voltage-dependent calcium channel and opioid receptor activation involved in nociceptive processing.
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Figure 1. Time course effects of intrathecally administered omega-conotoxin (omega-CgTx) in tail flick and mechanical paw pressure tests. Data are represented as mean+/-SEM from 5 or 6 rats.
Figure 1. Time course effects of intrathecally administered omega-conotoxin (omega-CgTx) in tail flick and mechanical paw pressure tests. Data are represented as mean+/-SEM from 5 or 6 rats.
Figure 1. Time course effects of intrathecally administered omega-conotoxin (omega-CgTx) in tail flick and mechanical paw pressure tests. Data are represented as mean+/-SEM from 5 or 6 rats.
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Figure 2. Dose-response lines for morphine and omega-conotoxin in the tail flick and the mechanical paw pressure tests. The data points represent the percent maximum possible effect seen 15 min after intrathecal administration of drugs. The number of observations at each point was 5–8. Data are mean+/-SEM.
Figure 2. Dose-response lines for morphine and omega-conotoxin in the tail flick and the mechanical paw pressure tests. The data points represent the percent maximum possible effect seen 15 min after intrathecal administration of drugs. The number of observations at each point was 5–8. Data are mean+/-SEM.
Figure 2. Dose-response lines for morphine and omega-conotoxin in the tail flick and the mechanical paw pressure tests. The data points represent the percent maximum possible effect seen 15 min after intrathecal administration of drugs. The number of observations at each point was 5–8. Data are mean+/-SEM.
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Figure 3. Effects of the combination of morphine and omega-conotoxin on tail flick latency (left) and mechanical paw pressure threshold (right). When a slightly effective dose of omega-CgTx (0.1 micro gram; open circles, n = 5) was combined with 2 micro gram of morphine (filled circles, n = 7), significant prolongation of TF latency and significant elevation of MPP threshold were shown (filled squares, n = 6). The effects of the combinations were reversed by intraperitoneally administered naloxone (200 micro gram/kg). Data for omega-CgTx alone are transferred from Figure 1. Data are mean+/-SEM. *P < 0.05 compared with morphine alone and omega-CgTx alone at individual times. (dagger)P < 0.05 compared with the percent maximum possible effect value 60 min after the intrathecal administration of the combination.
Figure 3. Effects of the combination of morphine and omega-conotoxin on tail flick latency (left) and mechanical paw pressure threshold (right). When a slightly effective dose of omega-CgTx (0.1 micro gram; open circles, n = 5) was combined with 2 micro gram of morphine (filled circles, n = 7), significant prolongation of TF latency and significant elevation of MPP threshold were shown (filled squares, n = 6). The effects of the combinations were reversed by intraperitoneally administered naloxone (200 micro gram/kg). Data for omega-CgTx alone are transferred from Figure 1. Data are mean+/-SEM. *P < 0.05 compared with morphine alone and omega-CgTx alone at individual times. (dagger)P < 0.05 compared with the percent maximum possible effect value 60 min after the intrathecal administration of the combination.
Figure 3. Effects of the combination of morphine and omega-conotoxin on tail flick latency (left) and mechanical paw pressure threshold (right). When a slightly effective dose of omega-CgTx (0.1 micro gram; open circles, n = 5) was combined with 2 micro gram of morphine (filled circles, n = 7), significant prolongation of TF latency and significant elevation of MPP threshold were shown (filled squares, n = 6). The effects of the combinations were reversed by intraperitoneally administered naloxone (200 micro gram/kg). Data for omega-CgTx alone are transferred from Figure 1. Data are mean+/-SEM. *P < 0.05 compared with morphine alone and omega-CgTx alone at individual times. (dagger)P < 0.05 compared with the percent maximum possible effect value 60 min after the intrathecal administration of the combination.
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Figure 4. Effects of the combination of morphine and omega-conotoxin at the dose of the 20:1 ratio, respectively. In tail flick and mechanical paw pressure tests, these combinations demonstrate a dose- and time-dependent prolongation of the latency and increase in the threshold, respectively. Data are mean+/-SEM.
Figure 4. Effects of the combination of morphine and omega-conotoxin at the dose of the 20:1 ratio, respectively. In tail flick and mechanical paw pressure tests, these combinations demonstrate a dose- and time-dependent prolongation of the latency and increase in the threshold, respectively. Data are mean+/-SEM.
Figure 4. Effects of the combination of morphine and omega-conotoxin at the dose of the 20:1 ratio, respectively. In tail flick and mechanical paw pressure tests, these combinations demonstrate a dose- and time-dependent prolongation of the latency and increase in the threshold, respectively. Data are mean+/-SEM.
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Figure 5. Isobolograms showing the interaction between morphine and omega-conotoxin in tail flick and mechanical paw pressure tests. In both isobolograms, the experimental points in both tests were observed below the theoretical additive points, indicating a synergistic interaction. Each point on the graph represent ED50values and 95% confidence intervals.
Figure 5. Isobolograms showing the interaction between morphine and omega-conotoxin in tail flick and mechanical paw pressure tests. In both isobolograms, the experimental points in both tests were observed below the theoretical additive points, indicating a synergistic interaction. Each point on the graph represent ED50values and 95% confidence intervals.
Figure 5. Isobolograms showing the interaction between morphine and omega-conotoxin in tail flick and mechanical paw pressure tests. In both isobolograms, the experimental points in both tests were observed below the theoretical additive points, indicating a synergistic interaction. Each point on the graph represent ED50values and 95% confidence intervals.
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Table 1. ED50and Total Fraction of Morphine and omega-Conotoxin in Tail Flick and Mechanical Paw Pressure Tests
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Table 1. ED50and Total Fraction of Morphine and omega-Conotoxin in Tail Flick and Mechanical Paw Pressure Tests
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