Koshiba H
Nihon Yakurigaku Zasshi. 1975 Jul;71(5):415-26.
Adrenaline and isoproterenol elicited nearly maximal relaxation of the colon even in small doses, whereas increase in the doses caused greater relaxation in the duodenum. In the colon, these drugs prevented, to a great extent the contraction induced by acetylcholine (ACh) and serotonin but in the duodenum were totally ineffective. Dibenamine and propranolol reduced adrenaline- and isoproterenol-induced relaxation in the duodenum, though propranolol decreased the relaxation caused by isoproterenol. Atropine prevented ACh-induced contraction in both the colon and duodenum in the same way. After 2-bromolysergic acid diethylamide, duodenal contraction caused by ACh or serotonin decreased by over 70%; however, the contraction of the colon was not significantly inhibited. Methysergide had similar effects, but to a lesser degree. In calcium-free bathing fluid without addition of Na2EDTA, ACh and prostaglandin E1 elicited contraction in the colon, but not in the duodenum.
肾上腺素和异丙肾上腺素即使小剂量也能引起结肠几乎最大程度的舒张,而剂量增加时十二指肠舒张程度更大。在结肠中,这些药物在很大程度上可防止乙酰胆碱(ACh)和5-羟色胺诱导的收缩,但在十二指肠中则完全无效。酚苄明和普萘洛尔可降低肾上腺素和异丙肾上腺素在十二指肠中引起的舒张,尽管普萘洛尔会降低异丙肾上腺素引起的舒张。阿托品以相同方式防止ACh在结肠和十二指肠中诱导的收缩。2-溴麦角酸二乙酰胺后,ACh或5-羟色胺引起的十二指肠收缩降低超过70%;然而,结肠的收缩未受到明显抑制。麦角新碱有类似作用,但程度较轻。在不添加Na2EDTA的无钙浴液中,ACh和前列腺素E1可引起结肠收缩,但不会引起十二指肠收缩。