Oriowo M A
Arch Int Pharmacodyn Ther. 1980 Jul;246(1):13-8.
The biphasic effect of amethocaine on the rat stomach strip was studied. Lower concentrations of amethocaine contracted the rat stomach strip. At higher concentrations, there was an initial contraction followed by a relaxation. When the tissue was partially contracted with carbachol (200 ng ml(-1)), all concentrations of amethocaine used produced a relaxation. The relaxation was not reduced by phentolamine (5 X 10(-6) g ml(-1)) but was abolished by propanolol (5 X 10(-6) g ml(-1)) which also blocked adrenaline-induced relaxation of the preparation. Treatment of the tissue with 6-OHDA (250 microgram ml(-1)) did not abolish the relaxation. It is suggested that amethocaine may relax the rat stomach strip by an action similar to beta-adrenoreceptor stimulation. This action of amethocaine may be independent of endogenous catecholamines.
研究了丁卡因对大鼠胃条的双相作用。较低浓度的丁卡因使大鼠胃条收缩。在较高浓度时,先是出现收缩,随后是舒张。当用卡巴胆碱(200 ng ml(-1))使组织部分收缩时,所用的所有浓度的丁卡因都会产生舒张作用。酚妥拉明(5×10(-6) g ml(-1))不会减弱这种舒张作用,但普萘洛尔(5×10(-6) g ml(-1))会消除这种舒张作用,普萘洛尔还会阻断肾上腺素诱导的该制剂的舒张。用6-羟基多巴胺(250微克 ml(-1))处理组织并不会消除这种舒张作用。提示丁卡因可能通过类似于β-肾上腺素能受体刺激的作用使大鼠胃条舒张。丁卡因的这种作用可能与内源性儿茶酚胺无关。