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药物对接种弗氏白血病病毒或刚地弓形虫的小鼠死亡率的影响。

The effect of drugs on the mortality of mice inoculated with Friend leukaemia virus or toxoplasma gondii.

作者信息

Starec M, Sinet M, Kodym P, Rosina J, Fiserová A, Desforges B, Rouveix B

机构信息

Department of Pharmacology, Third Medical Faculty, Charles University, Prague, Czech Republic.

出版信息

Physiol Res. 1997;46(2):107-11.

PMID:9727501
Abstract

Infection and tumors provoke substantial changes accompanied with the disbalance of many neuroendocrine factors which in their summarizing effects influence the life span of animals. Our previous results showed enhanced mortality after one injection of morphine in association with Friend leukaemia virus infection. The aim of this study was to examine the effects of some other opioids (pethidine and pentazocine) and an acetylcholine esterase inhibitor neostigmine on the survival of animals under two conditions: (1) Friend leukaemia virus infection which mostly depressed immune functions, and (2) Toxoplasma gondii infection which in general enhanced the immune status. In contrast to our previous observation with morphine, the mortality induced by single doses of pethidine (150 mg/kg) or pentazocine (50-75 mg/kg) was unchanged during the Friend leukaemia virus infection. A single injection of neostigmine (0.42 or 0.56 mg/kg) was significantly more lethal in DBA-2 mice infected with Friend leukaemia virus. Neostigmine in doses of 0.33 and 0.4 mg/kg caused death in 46 % and 57 %, respectively, of animals infected with Toxoplasma gondii which was significantly higher in comparison with only 8 % and 12.5 % in control groups. Pethidine (150 mg/kg) killed 70 % of Toxoplasma gondii infected animals and even 90 % of non-infected mice. Thus, the Friend leukaemia virus and Toxoplasma gondii infections increased toxicity only of some drugs which may, at least partly, be associated with altered immune status during infection and involvement of the cholinergic system.

摘要

感染和肿瘤会引发重大变化,并伴随着许多神经内分泌因子的失衡,这些因子的综合作用会影响动物的寿命。我们之前的研究结果表明,单次注射吗啡后,与Friend白血病病毒感染相关的死亡率会升高。本研究的目的是在两种情况下,研究其他一些阿片类药物(哌替啶和喷他佐辛)以及乙酰胆碱酯酶抑制剂新斯的明对动物存活的影响:(1)主要抑制免疫功能的Friend白血病病毒感染;(2)总体上增强免疫状态的弓形虫感染。与我们之前对吗啡的观察结果相反,在Friend白血病病毒感染期间,单剂量哌替啶(150mg/kg)或喷他佐辛(50-75mg/kg)诱导的死亡率没有变化。单次注射新斯的明(0.42或0.56mg/kg)对感染Friend白血病病毒的DBA-2小鼠的致死性明显更高。剂量为0.33和0.4mg/kg的新斯的明分别导致46%和57%的弓形虫感染动物死亡,这与对照组仅8%和12.5%的死亡率相比显著更高。哌替啶(150mg/kg)导致70%的弓形虫感染动物死亡,甚至90%的未感染小鼠死亡。因此,Friend白血病病毒和弓形虫感染仅增加了某些药物的毒性,这可能至少部分与感染期间免疫状态的改变以及胆碱能系统的参与有关。

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