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(+)-吗啡相对于(-)-吗啡在通过小鼠体内纳洛酮敏感的σ受体减弱(-)-吗啡产生的抗伤害感受方面的立体选择性作用。

Stereoselective action of (+)-morphine over (-)-morphine in attenuating the (-)-morphine-produced antinociception via the naloxone-sensitive sigma receptor in the mouse.

作者信息

Wu Hsiang-en, Hong Jau-Shyong, Tseng Leon F

机构信息

Department of Anesthesiology, Medical College of Wisconsin, Milwaukee, WI 53226, USA.

出版信息

Eur J Pharmacol. 2007 Oct 1;571(2-3):145-51. doi: 10.1016/j.ejphar.2007.06.012. Epub 2007 Jun 21.

Abstract

We have previously demonstrated that (+)-morphine and (-)-morphine given spinally stereoselectively attenuate the spinally-administered (-)-morphine-produced tail-flick inhibition in the mouse. The phenomenon has been defined as antianalgesia. Present studies were then undertaken to determine if the systemic administration of (+)-morphine and (-)-morphine also stereoselectively attenuates the systemic (-)-morphine-produced tail-flick inhibition and the effects of (+)-morphine and (-)-morphine are mediated by the naloxone-sensitive sigma receptor activation in male CD-1 mice. Pretreatment with (+)-morphine at a dose of 0.01-10 ng/kg given subcutaneously dose-dependently attenuated the tail-flick inhibition produced by subcutaneously-administered (-)-morphine (5 mg/kg). Pretreatment with (-)-morphine (0.01-1.0 mg/kg) given subcutaneously also attenuates the (-)-morphine-produced tail-flick inhibition. The ED50 values for (+)-morphine and (-)-morphine for inhibiting the (-)-morphine-produced tail-flick inhibition were estimated to be 30.6 pg/kg and 97.5 microg/kg, respectively. The attenuation of the (-)-morphine-produced tail-flick inhibition induced by (+)-morphine or (-)-morphine pretreatment was reversed by the pretreatment with (+)-naloxone or by the sigma receptor antagonist BD1047 (N-[2-(3,4-dichlorophenyl)ethyl]-N-methyl-2-(dimethylamino)ethylamine dihydrobromide) given subcutaneously. Pretreatment with (+)-pentazocine, a selective sigma receptor agonist, (1-10 mg/kg) given subcutaneously also attenuates (-)-morphine-produced tail-flick inhibition, which was restored by (+)-naloxone (4 mg/kg) or BD1047 (10 mg/kg) pretreated subcutaneously. It is concluded that (+)-morphine exhibits extremely high stereoselective action over (-)-morphine given systemically in attenuating the systemic (-)-morphine-produced antinociception and the antianalgesic effect of (+)-morphine and (-)-morphine is mediated by activation of the naloxone-sensitive sigma receptor.

摘要

我们之前已经证明,脊髓给予(+)-吗啡和(-)-吗啡可立体选择性地减弱脊髓给予(-)-吗啡在小鼠中产生的甩尾抑制。这种现象被定义为抗镇痛作用。随后进行了本研究,以确定全身给予(+)-吗啡和(-)-吗啡是否也能立体选择性地减弱全身给予(-)-吗啡产生的甩尾抑制,以及(+)-吗啡和(-)-吗啡的作用是否由雄性CD-1小鼠中对纳洛酮敏感的σ受体激活介导。皮下给予剂量为0.01 - 10 ng/kg的(+)-吗啡预处理,剂量依赖性地减弱了皮下给予(-)-吗啡(5 mg/kg)产生的甩尾抑制。皮下给予(-)-吗啡(0.01 - 1.0 mg/kg)预处理也减弱了(-)-吗啡产生的甩尾抑制。(+)-吗啡和(-)-吗啡抑制(-)-吗啡产生的甩尾抑制的ED50值分别估计为30.6 pg/kg和97.5 μg/kg。(+)-纳洛酮预处理或皮下给予σ受体拮抗剂BD1047(N-[2-(3,4-二氯苯基)乙基]-N-甲基-2-(二甲基氨基)乙胺二氢溴化物)可逆转(+)-吗啡或(-)-吗啡预处理诱导的(-)-吗啡产生的甩尾抑制减弱。皮下给予选择性σ受体激动剂(+)-喷他佐辛(1 - 10 mg/kg)预处理也减弱了(-)-吗啡产生的甩尾抑制,皮下给予(+)-纳洛酮(4 mg/kg)或BD1047(10 mg/kg)可恢复该抑制。结论是,在减弱全身给予(-)-吗啡产生的抗伤害感受方面,(+)-吗啡对全身给予的(-)-吗啡表现出极高的立体选择性作用,并且(+)-吗啡和(-)-吗啡的抗镇痛作用是由对纳洛酮敏感的σ受体激活介导的。

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