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慢性锂预处理对阿扑吗啡诱导的阴茎勃起的影响。

Effects of chronic lithium pretreatment on apomorphine-induced penile erection.

作者信息

Dehpour A R, Samini M, Sharifzadeh M, Hasan-Mazandarani H

机构信息

Department of Pharmacology, Faculty of Medicine, Tehran University of Medical Sciences, Iran.

出版信息

Gen Pharmacol. 1995 Sep;26(5):1015-20. doi: 10.1016/0306-3623(94)00276-s.

DOI:10.1016/0306-3623(94)00276-s
PMID:7557243
Abstract
  1. The effects of chronic lithium pretreatment (600 mg/l in drinking rats, 30 days) on penile erection (PE) induced by apomorphine were investigated in rats. This treatment resulted in a serum Li concentration after 30 days of 0.31 +/- 0.01 mmol/l. 2. Subcutaneous (s.c.) administration of mixed D1/D2 dopamine receptor agonist apomorphine (0.05-0.5 mg/kg) induced PE in a biphasic manner. The maximum effect was obtained with 0.1 mg/kg of the drug while the response decreased with increasing doses of apomorphine from 0.1 to 0.5 mg/kg. 3. Pretreatment of animals with 0.0125-0.1 mg/kg of D1 dopamine receptor antagonist SCH 23390 or D2 dopamine receptor antagonist sulpiride (12.5-100 mg/kg) decreased apomorphine-induced PE. Combination of SCH 23390 (0.025 mg/ kg) with sulpiride (12.5 mg/kg) caused a stronger inhibitory effect on apomorphine response. This indicates that both D1 and D2 dopamine receptors may be involved in PE induced by apomorphine. 4. The response induced by apomorphine (0.05-0.05 mg/kg) was decreased in animals pretreated with chronic lithium. The inhibitory effect of sulpiride on apomorphine response, increased in animals pretreated with lithium, in contrast the inhibitory effect of SCH 23390 did not change in this condition. However, a combination of SCH 23390 with sulpiride increased inhibitory effect on apomorphine response in lithium pretreated rats. 5. It is concluded that chronic lithium inhibits PE induced by dopaminergic mechanism(s).
摘要
  1. 研究了慢性锂预处理(饮水中含600mg/l,对大鼠进行30天)对阿扑吗啡诱导的大鼠阴茎勃起(PE)的影响。该处理30天后导致血清锂浓度为0.31±0.01mmol/l。2. 皮下(s.c.)注射混合的D1/D2多巴胺受体激动剂阿扑吗啡(0.05 - 0.5mg/kg)以双相方式诱导阴茎勃起。药物剂量为0.1mg/kg时获得最大效应,而随着阿扑吗啡剂量从0.1mg/kg增加到0.5mg/kg,反应减弱。3. 用0.0125 - 0.1mg/kg的D1多巴胺受体拮抗剂SCH 23390或D2多巴胺受体拮抗剂舒必利(12.5 - 100mg/kg)对动物进行预处理可降低阿扑吗啡诱导的阴茎勃起。SCH 23390(0.025mg/kg)与舒必利(12.5mg/kg)联合使用对阿扑吗啡反应产生更强的抑制作用。这表明D1和D2多巴胺受体可能都参与了阿扑吗啡诱导的阴茎勃起。4. 慢性锂预处理的动物中,阿扑吗啡(0.05 - 0.05mg/kg)诱导的反应减弱。锂预处理的动物中,舒必利对阿扑吗啡反应的抑制作用增强,相比之下,SCH 23390在这种情况下的抑制作用没有变化。然而,SCH 23390与舒必利联合使用可增强对锂预处理大鼠阿扑吗啡反应的抑制作用。5. 得出结论:慢性锂抑制多巴胺能机制诱导的阴茎勃起。

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