Albuquerque M L, Kurth C D
Department of Anesthesiology, Children's Hospital of Philadelphia, PA.
Eur J Pharmacol. 1993 Nov 9;249(2):215-20. doi: 10.1016/0014-2999(93)90435-k.
The effect of cocaine on cerebral arterioles was determined in newborn pigs and the mechanism of action was examined in terms of its local anesthetic and sympathomimetic properties. Forty-three newborn piglets were anesthetized, equipped with a closed cranial window, and the diameter of pial arterioles was measured by intravital microscopy. Increasing concentrations of cocaine (10(-7) M to 10(-3) M) applied onto the cortical surface resulted in a dose-dependent decrease in arteriolar diameter. Coadministration with phentolamine, an alpha-adrenoceptor antagonist, did not inhibit the contractile response to cocaine even though phentolamine blocked the constriction to topically applied norepinephrine. In contrast, coadministration of either tetrodotoxin (Na+ channel blocker), charybdotoxin (K+ channel blocker), or quinacrine (phospholipase A2 inhibitor), or pretreatment with indomethacin (cyclooxygenase inhibitor) attenuated vasoconstriction induced by cocaine. Topically applied lidocaine (10(-7) M to 10(-3) M), a local anesthetic without sympathomimetic properties, caused a dose-dependent constriction similar to cocaine, whereas topically applied nomifensine and desipramine (each 10(-7) M to 10(-3) M), inhibitors of dopamine and norepinephrine re-uptake, respectively, did not constrict cerebral arterioles. These results indicate that cocaine constricts cerebral arterioles by its local anesthetic properties rather than its sympathomimetic properties. The mechanism appears to involve an alteration in the flux of Na+ or K+ or prostanoid metabolism.
在新生猪中测定了可卡因对脑小动脉的作用,并根据其局部麻醉和拟交感神经特性研究了其作用机制。43只新生仔猪接受麻醉,安装封闭的颅窗,通过活体显微镜测量软脑膜小动脉的直径。将浓度不断增加的可卡因(10⁻⁷M至10⁻³M)应用于皮质表面,导致小动脉直径呈剂量依赖性减小。与α-肾上腺素能受体拮抗剂酚妥拉明共同给药,即使酚妥拉明阻断了对局部应用去甲肾上腺素的收缩反应,也不能抑制对可卡因的收缩反应。相比之下,共同给予河豚毒素(钠通道阻滞剂)、蝎毒素(钾通道阻滞剂)或奎纳克林(磷脂酶A2抑制剂),或用吲哚美辛(环氧化酶抑制剂)预处理,均可减弱可卡因诱导的血管收缩。局部应用利多卡因(10⁻⁷M至10⁻³M),一种无拟交感神经特性的局部麻醉药,引起与可卡因相似的剂量依赖性收缩,而局部应用诺米芬辛和地昔帕明(均为10⁻⁷M至10⁻³M),分别为多巴胺和去甲肾上腺素再摄取抑制剂,并不使脑小动脉收缩。这些结果表明,可卡因通过其局部麻醉特性而非拟交感神经特性使脑小动脉收缩。其机制似乎涉及钠或钾通量的改变或前列腺素代谢。