García-Villalón A L, Fernández N, García J L, Monge L, Gómez B, Diéguez G
Departamento de Fisiología, Facultad de Medicina, Universidad Autónoma, Madrid, Spain.
Pflugers Arch. 1993 Nov;425(3-4):256-62. doi: 10.1007/BF00374175.
The cavernous carotid artery, that portion of the internal carotid artery that lies within the intracranial cavernous sinus, is covered by arterial (luminal surface) and venous (external surface) endothelium. The reactivity of the isolated canine, cavernous carotid artery, precontracted with 10(-5) M 5-hydroxytryptamine, was studied by using in vitro perfusion and superfusion to evaluate the effects of vasoactive stimuli applied to the internal or external surface. Acetylcholine (10(-8)-10(-4) M), thrombin (0.01-1 U/ml) or calcium ionophore A23187 (10(-8) - 10(-6) M) on the luminal side produced concentration-dependent relaxations which were reduced by the NO synthase inhibitor NG-nitro-L-arginine methyl ester (L-NAME, 10(-4) M) or by removing either the internal or both endothelia. Thrombin or ionophore A23187 on the external side produced concentration-dependent contractions which were reduced by removing either the external or both endothelia, and by meclofenamate (10(-5) M). Acetylcholine on the external side, produced a concentration-dependent contraction that was unaffected by meclofenamate or by removing the external or both endothelia. Sodium nitroprusside (10(-7) - 10(-5) M) induced similar relaxation on both sides and regardless of whether the arteries were with or without endothelium. These results suggest firstly, that the cavernous carotid artery responds to acetylcholine, thrombin or calcium ionophore A23187 by relaxing or contracting when these agents act on the luminal or the external surface respectively. Secondly, the arterial endothelium mediates relaxation to these three substances by releasing NO, whereas the venous endothelium mediates contraction to thrombin and ionophore A23187 by releasing a cyclooxygenase product.(ABSTRACT TRUNCATED AT 250 WORDS)
海绵窦段颈内动脉,即位于颅内海绵窦内的颈内动脉部分,其管腔内表面(动脉面)和外表面(静脉面)均覆盖有内皮细胞。使用离体灌注和超灌注方法,研究了预先用10⁻⁵ M 5-羟色胺预收缩的犬离体海绵窦段颈内动脉的反应性,以评估施加于内表面或外表面的血管活性刺激的作用。乙酰胆碱(10⁻⁸ - 10⁻⁴ M)、凝血酶(0.01 - 1 U/ml)或钙离子载体A23187(10⁻⁸ - 10⁻⁶ M)作用于管腔内表面时可产生浓度依赖性舒张,一氧化氮合酶抑制剂NG-硝基-L-精氨酸甲酯(L-NAME,10⁻⁴ M)或去除内皮层或同时去除内外皮层均可减弱这种舒张。凝血酶或离子载体A23187作用于外表面时可产生浓度依赖性收缩,去除外皮层或同时去除内外皮层以及使用甲氯芬那酸(10⁻⁵ M)均可减弱这种收缩。乙酰胆碱作用于外表面时可产生浓度依赖性收缩,甲氯芬那酸或去除外皮层或同时去除内外皮层对此均无影响。硝普钠(10⁻⁷ - 10⁻⁵ M)在两侧均可诱导相似的舒张,且无论动脉有无内皮均有此作用。这些结果表明,首先,当乙酰胆碱、凝血酶或钙离子载体A23187分别作用于海绵窦段颈内动脉的管腔内表面或外表面时,该动脉会通过舒张或收缩做出反应。其次,动脉内皮通过释放一氧化氮介导对这三种物质的舒张反应,而静脉内皮通过释放环氧化酶产物介导对凝血酶和离子载体A23187的收缩反应。(摘要截选至250词)