Manzini S, Perretti F
Istituto Farmacobiologico Malesci S.p.A., Pharmacology Department, Florence, Italy.
Eur J Pharmacol. 1988 Mar 29;148(2):153-9. doi: 10.1016/0014-2999(88)90559-6.
The effects of intra- and extraluminal capsaicin administration were evaluated in isolated perfused rat mesenteric bed. Capsaicin (10 nM-1 microM) produced a potent concentration-dependent relaxation of the tonic vasoconstriction induced by norepinephrine (1 microM) but not by high-K+ (60 mM). The capsaicin-induced relaxation was nearly abolished in preparations pretreated in vitro with a high concentration of capsaicin (1 microM, for 10 min, 1 h before). Capsaicin-induced relaxation was reduced but not abolished in preparations obtained from rats pretreated neonatally with capsaicin. The capsaicin effects were unaffected by atropine, guanethidine, propranolol, hexamethonium or tetrodotoxin. The observation that capsaicin (0.1 microM)-induced relaxation was virtually abolished in presence of the proteolytic enzyme alpha-chymotrypsin (1 U/ml) supports the involvement of neuropeptide(s) in this response. Bolus injections of calcitonin gene-related peptide (CGRP) elicited a potent and rapidly ensuing relaxation which underwent tachyphylaxis. However, no cross-desensitization with capsaicin was observed. It is concluded that activation of capsaicin-sensitive sensory fibers could release neuropeptides locally with a potent effect on intestinal blood flow.
在离体灌注的大鼠肠系膜床中评估了腔内和腔外给予辣椒素的效果。辣椒素(10 nM - 1 μM)可使去甲肾上腺素(1 μM)诱导的强直性血管收缩产生强效的浓度依赖性舒张,但对高钾(60 mM)诱导的血管收缩无此作用。在体外预先用高浓度辣椒素(1 μM,处理10分钟,提前1小时)处理的标本中,辣椒素诱导的舒张几乎完全消失。在新生期用辣椒素预处理的大鼠所获得的标本中,辣椒素诱导的舒张有所减弱但并未消失。辣椒素的作用不受阿托品、胍乙啶、普萘洛尔、六甲铵或河豚毒素的影响。在存在蛋白水解酶α - 糜蛋白酶(1 U/ml)的情况下,辣椒素(0.1 μM)诱导的舒张几乎完全消失,这一观察结果支持了神经肽参与这一反应。推注降钙素基因相关肽(CGRP)可引发强效且迅速出现的舒张,且出现快速耐受性。然而,未观察到与辣椒素的交叉脱敏现象。得出的结论是,激活辣椒素敏感的感觉纤维可在局部释放神经肽,对肠血流量产生强效作用。