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甲基苯丙胺对大鼠离体输精管抽搐反应的影响。

Effects of methamphetamine on the twitch response in the rat isolated vas deferens.

作者信息

Urabe M, Kawasaki H, Takasaki K

机构信息

Department of Pharmacology, Miyazaki Medical College, Japan.

出版信息

Jpn J Pharmacol. 1987 Nov;45(3):357-64. doi: 10.1254/jjp.45.357.

Abstract

The effect of methamphetamine, an indirectly acting sympathomimetic amine, on presynaptic adrenergic regulation in isolated rat vas deferens was studied by comparing it with those of tyramine, cocaine and clonidine. These drugs markedly attenuated the twitch response to electrical field stimulation in a concentration-dependent manner. The relative order of potency for the drugs was: clonidine (10(-10)-3 x 10(-8) M) greater than methamphetamine (10(-8)-3 x 10(-6) M) greater than tyramine (10(-7)-10(-4) M) greater than cocaine (10(-6)-3 x 10(-5) M). Only tyramine (3 x 10(-6)-10(-4) M) elicited a concentration-dependent contractile response, which was abolished by prazosin (10(-6) M) and the reserpinization. The twitch inhibitory effect of these drugs was antagonized by yohimbine (10(-8)-10(-6) M). Both the methamphetamine- and tyramine-induced twitch inhibition were partially (about 50%) attenuated by chronic reserpinization (3 mg/kg, s.c., twice) in combination with alpha-methyl-p-tyrosine (200 mg/kg, s.c., twice), while the clonidine-induced inhibition was not affected by this application at all, and the cocaine-induced twitch inhibition was abolished by the reserpinization. Both the clonidine- and tyramine-induced twitch inhibition were not affected by pretreatment with cocaine (10(-5) M) in combination with estradiol (4 x 10(-5) M), whereas the effect of methamphetamine was slightly attenuated. These results suggest that methamphetamine as well as tyramine and cocaine indirectly activates presynaptic alpha-2 adrenoceptors via norepinephrine released from adrenergic nerves to inhibit the twitch response.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

通过将甲基苯丙胺(一种间接作用的拟交感胺)与酪胺、可卡因和可乐定进行比较,研究了其对离体大鼠输精管突触前肾上腺素能调节的影响。这些药物以浓度依赖性方式显著减弱对电场刺激的抽搐反应。药物的效力相对顺序为:可乐定(10^(-10)-3×10^(-8)M)>甲基苯丙胺(10^(-8)-3×10^(-6)M)>酪胺(10^(-7)-10^(-4)M)>可卡因(10^(-6)-3×10^(-5)M)。只有酪胺(3×10^(-6)-10^(-4)M)引起浓度依赖性收缩反应,该反应被哌唑嗪(10^(-6)M)和利血平化所消除。这些药物的抽搐抑制作用被育亨宾(10^(-8)-10^(-6)M)拮抗。甲基苯丙胺和酪胺诱导的抽搐抑制在慢性利血平化(3mg/kg,皮下注射,两次)联合α-甲基-对酪氨酸(200mg/kg,皮下注射,两次)时部分(约50%)减弱,而可乐定诱导的抑制完全不受此处理影响,可卡因诱导的抽搐抑制被利血平化消除。可乐定和酪胺诱导的抽搐抑制不受可卡因(10^(-5)M)联合雌二醇(4×10^(-5)M)预处理的影响,而甲基苯丙胺的作用略有减弱。这些结果表明,甲基苯丙胺以及酪胺和可卡因通过肾上腺素能神经释放的去甲肾上腺素间接激活突触前α-2肾上腺素能受体以抑制抽搐反应。(摘要截断于250字)

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