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[一项使用速效药物的药物依赖性研究]

[A study on drug dependence using fast acting drugs].

作者信息

Yanaura S, Tagashire E, Izumi T

出版信息

Nihon Yakurigaku Zasshi. 1975 May;71(4):329-37.

PMID:1237448
Abstract

Physical dependence on narcotics is induced in laboratory animals by intermittent parenteral administration (2 approximately 3 times daily). However, inducing of dependence on pethidine has been unsuccessful using the parenteral method. Recently, it has been reported that physical dependence on pethidine can be induced by continuous infusion methods (5.6). In the present experiment, pethidine was administered to rats (n=5 approximately 6) by ingestion of pethidine-admixed food preparations (0.5 approximately 4.0 mg/g of feed). The results indicated that (a) when rats are allowed free access to two food preparations (0.5 mg/g vs. 1 mg/g of food) for 7 weeks, spontaneous intake ratios of food (1 mg/g of food) gradually increased from 15% to 30% after 3 weeks. (b) Abrupt withdrawal for 48 hr after a 10 day administration period (2 mg/g of food on day 1 approximately 3 and 4 mg/g of food on day 4 approximately 10) resulted in a loss of body weight in the next 24 hr, and the prewithdrawal level of body weight was recovered in 48 hr. (c) The time course of body weight and food intake during the first 24 hr withdrawal period demonstrated the characteristic pattern of abstinence syndrome of pethidine, viz. early onset (12 approximately 13 hr) and rapid recovery (within 48 hr), as compared to morphine withdrawal. (d) Suppression of pethidine abstinence of both a single injection of morphine (10 mg/kg, s.c.) and substitution for morphine-admixed food was also realized. (e) When levallorphan (5 mg/kg, s.c.) was administered to both pethidine and morphine dependence rats, the maximal decrease in body weight was less than that in morphine dependent rats. These data indicate that pethidine possesses about one fifth the dependence liability of morphine and the maximal abstinence syndrome appears within 24 hr after withdrawal. Conclusively, application of a drug-admixed food preparation in drug dependence tests in rats has proven to be a useful method, particularly in the case of pethidine-like drugs which rapidly disappear from the blood.

摘要

通过间歇性肠胃外给药(每天约2至3次)可使实验动物对麻醉药品产生身体依赖性。然而,采用肠胃外给药方法诱导对哌替啶的依赖性并未成功。最近,有报道称通过持续输注法(5,6)可诱导对哌替啶的身体依赖性。在本实验中,通过给大鼠(n = 5至6只)喂食掺有哌替啶的食物制剂(0.5至4.0毫克/克饲料)来给予哌替啶。结果表明:(a) 当大鼠可自由获取两种食物制剂(0.5毫克/克食物与1毫克/克食物)达7周时,食物(1毫克/克食物)的自发摄入比例在3周后从15%逐渐增加至30%。(b) 在10天给药期(第1天至第3天为2毫克/克食物,第4天至第10天为4毫克/克食物)后突然停药48小时,导致大鼠在接下来的24小时内体重减轻,且在48小时内恢复到停药前的体重水平。(c) 在最初24小时停药期内体重和食物摄入的时间进程显示出哌替啶戒断综合征的特征模式,即与吗啡戒断相比,起效早(12至13小时)且恢复快(48小时内)。(d) 单次注射吗啡(10毫克/千克,皮下注射)以及用掺有吗啡的食物替代均可抑制哌替啶戒断。(e) 当给哌替啶和吗啡依赖的大鼠都注射左洛啡烷(5毫克/千克,皮下注射)时,体重的最大降幅小于吗啡依赖大鼠。这些数据表明,哌替啶的依赖性倾向约为吗啡的五分之一,且最大戒断综合征在停药后24小时内出现。总之,在大鼠药物依赖性试验中应用掺有药物的食物制剂已被证明是一种有用的方法,特别是对于像哌替啶这类会迅速从血液中消失的药物而言。

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