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Correspondence  |   June 1996
Vasomotor Effects of Isoflurane in the Coronary Circulation
Author Notes
  • Kyung W. Park, Instructor in Anaesthesia, Harvard Medical School.
  • Edward Lowenstein, Professor of Anaesthesia, Harvard Medical School, Anesthetist-in-chief, Beth Israel Hospital.
  • Frank W. Sellke, Associate Professor of Surgery, Harvard Medical School, Beth Israel Hospital, 330 Brookline Avenue, Boston, Massachussets 02215.
Article Information
Correspondence
Correspondence   |   June 1996
Vasomotor Effects of Isoflurane in the Coronary Circulation
Anesthesiology 6 1996, Vol.84, 1517-1518. doi:0000542-199606000-00035
Anesthesiology 6 1996, Vol.84, 1517-1518. doi:0000542-199606000-00035
In Reply:--Although Crystal questions whether isoflurane-induced vasoconstriction of resistance coronary arteries is a preparation-dependent phenomenon without wide-ranging application, we have gathered multiples pieces of evidence to the contrary. First, this phenomenon has been observed in four different species--namely, rabbits, [1] rats, [2] pigs, [3] and human right atrial appendage arteries (Figure 1). However, the effect of isoflurane depends on vessel size, and isoflurane dilates large epicardial arteries. [1,2] Second, isoflurane has been observed to attenuate beta-adrenergic, cAMP-mediated vasodilation [4] in resistance coronary arteries. Third, in the same preparation, another anesthetic, halothane, [2] does not elicit constriction, but dilation, of resistance coronary arteries. We submit that the weight of evidence favors that the direct effect of isoflurane on small resistance coronary arteries ([nearly equal] 100 micro meter) is constriction but depends on preexposure tone. [2] .
Figure 1. Percent change from baseline diameter versus concentration of isoflurane for resistance coronary arteries from four species. Data are presented as mean+/-SD. Isoflurane caused concentration-dependent constriction of resistance coronary arteries in all four species (P < 0.05 for each).
Figure 1. Percent change from baseline diameter versus concentration of isoflurane for resistance coronary arteries from four species. Data are presented as mean+/-SD. Isoflurane caused concentration-dependent constriction of resistance coronary arteries in all four species (P < 0.05 for each).
Figure 1. Percent change from baseline diameter versus concentration of isoflurane for resistance coronary arteries from four species. Data are presented as mean+/-SD. Isoflurane caused concentration-dependent constriction of resistance coronary arteries in all four species (P < 0.05 for each).
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The apparent discrepancy between our in vitro findings of isoflurane-induced constriction of resistance coronary arteries and multiple in vivo studies suggestive of isoflurane-mediated dilation of resistance coronary arteries [5,6] has been discussed extensively in our papers. [1,2] We will not reiterate this here. In vivo studies such as by Crystal et al. [5] measure changes in myocardial blood flow (MBF) as a surrogate for small resistance artery vasomotion. Merely measuring changes in MBF does not indicate the vascular site of isoflurane-mediated effect. An increase in MBF may represent dilation of small resistance coronary arteries, dilation of larger arteries, and/or increase in nonnutritive shunting. A mild to modest increase in MBF that is reported in most in vivo studies (The studies by Crystal's group are an exception in this regard in that they report a nearly maximal increase in MBF with isoflurane.) can be explained easily without invoking primary dilation of resistance coronary arteries. Dilation of large arteries, which is reported to occur in both our preparation [1,2] and that of others, [7] will have a magnified effect on flow because of flow-mediated release of nitric oxide, [8] and the vascular resistance will decrease more than would be predicted just based on diameter changes of the large vessels. Alternatively, an increase in coronary shunting will yield an increase in MBF even without dilation of resistance coronary arteries.
Two representative microsphere studies that addressed coronary shunting with isoflurane anesthesia are those of Crystal et al. [5] and Gelman et al. [9] Unlike the impression Crystal received, our intention [2] was not to compare the relative merits of the two studies and declare one superior to the other. Our intention was to point out the uncertainty of ascertaining the degree of shunting with microsphere methods. Various sources of error in measuring regional blood flows with radioactive microspheres reduce precision of estimate (i.e., large SDs and P value) but do not lead to a systematic over- or underestimation of mean flow. [10,11] In addition, venous sampling of microspheres, as was done by Crystal et al., [5] has been demonstrated to underestimate the amount of shunting, compared with direct tissue sampling. [12] .
In the canine circulation, studied by Crystal et al. [5] and Gelman et al., [9] the diameter of the capillaries is 3–8 micro meter. [11] Gelman et al. [9] implied that entrapment of 9-micro meter microspheres represents nutritive flow through the capillaries, and entrapment of 15-micro meter microspheres represents nutritive and nonnutritive flow, and therefore, the difference in flows measured represents shunted flow through arteriovenous anastomoses of approximately 10–15 micro meter. They noted a threefold increase in shunting under 2 MAC isoflurane anesthesia, although this increase did not achieve statistical significance. As Crystal seems to imply in his letter, Gelman et al.'s methods may ignore any shunts greater than approximately 15 micro meter.
In conclusion, our finding of direct vasoconstrictive effect of isoflurane on resistance coronary arteries appears a real phenomenon that has been observed in four species. It is unique to isoflurane among the anesthetics thus far examined and largely depends on the tone of the vessels. How this finding should be reconciled with in vivo increases in myocardial blood flow with isoflurane awaits further work.
Kyung W. Park, M.D., Instructor in Anaesthesia, Harvard Medical School.
Edward Lowenstein, M.D., Professor of Anaesthesia, Harvard Medical School, Anesthetist-in-chief, Beth Israel Hospital.
Frank W. Sellke, M.D., Associate Professor of Surgery, Harvard Medical School, Beth Israel Hospital, 330. Brookline Avenue, Boston, Massachusetts 02215.
REFERENCES
Park KW, Dai HB, Lowenstein E, Darvish A, Sellke FW: Heterogeneous vasomotor responses of rabbit coronary microvessels to isoflurane. ANESTHESIOLOGY 1994; 81:1190-7.
Park KW, Dai HB, Lowenstein E, Sellke FW: Vasomotor responses of rat coronary arteries to isoflurane and halothane depend on preexposure tone and vessel size. ANESTHESIOLOGY 1995; 83:1323-30.
Park KW, Dai HB, Lowenstein E, Sellke FW: Comparison of direct vasomotor effect of isoflurane in normal and collateral-dependent coronary microvessels in pigs (abstract). Anesth Analg 1996; 82:SCA126.
Park KW, Dai HB, Lowenstein E, Darvish A, Sellke FW: Isoflurane attenuates cAMP-mediated vasodilation in rat microvessels. Circulation 1995; 92(suppl 2):II423-7.
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Figure 1. Percent change from baseline diameter versus concentration of isoflurane for resistance coronary arteries from four species. Data are presented as mean+/-SD. Isoflurane caused concentration-dependent constriction of resistance coronary arteries in all four species (P < 0.05 for each).
Figure 1. Percent change from baseline diameter versus concentration of isoflurane for resistance coronary arteries from four species. Data are presented as mean+/-SD. Isoflurane caused concentration-dependent constriction of resistance coronary arteries in all four species (P < 0.05 for each).
Figure 1. Percent change from baseline diameter versus concentration of isoflurane for resistance coronary arteries from four species. Data are presented as mean+/-SD. Isoflurane caused concentration-dependent constriction of resistance coronary arteries in all four species (P < 0.05 for each).
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