THE EFFECT OF DRUGS ON THE MORTALITY OF MICE INOCULATED WITH FRIEND-LEUKEMIA VIRUS OR TOXOPLASMA-GONDII

Citation
M. Starec et al., THE EFFECT OF DRUGS ON THE MORTALITY OF MICE INOCULATED WITH FRIEND-LEUKEMIA VIRUS OR TOXOPLASMA-GONDII, Physiologia bohemoslovaca, 46(2), 1997, pp. 107-111
Citations number
20
Journal title
ISSN journal
03699463
Volume
46
Issue
2
Year of publication
1997
Pages
107 - 111
Database
ISI
SICI code
0369-9463(1997)46:2<107:TEODOT>2.0.ZU;2-A
Abstract
Infection and tumors provoke substantial changes accompanied with the disbalance of many neuroendocrine factors which in their summarizing e ffects influence the life span of animals. Our previous results showed enhanced mortality after one injection of morphine in association wit h Friend leukaemia virus infection. The aim of this study was to exami ne the effects of some other opioids (pethidine and pentazocine) and a n acetylcholine esterase inhibitor neostigmine on the survival of anim als under two conditions: (1) Friend leukaemia virus infection which m ostly depressed immune functions, and (2) Toxoplasma gondii infection which in general enhanced the immune status. In contrast to our previo us observation with morphine, the mortality induced by single doses of pethidine (150 mg/kg) or pentazocine (50-75 mg/kg) was unchanged duri ng the Friend leukaemia virus infection. A single injection of neostig mine (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 inf ected with Toxoplasma gondii which was significantly higher in compari son 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.