Akademik Veri Yönetim Sistemi
PHARMACOLOGY, cilt.62, sa.1, ss.36-44, 2001 (SCI-Expanded)
The cardiovascular effects of tetrahydroaminoacridine (tacrine; THA) were investigated in haemorrhaged rats. Intracerebroventricular (i.c.v.) injection of THA (10, 25 and 50 mug) restored blood pressure in a dose- and time-dependent manner. Atropine (10 mug, i.c.v.), a muscarinic receptor antagonist, attenuated the presser response to THA (25 mug, i.c.v.), while mecamylamine (50 mug, i.c.v.), a nicotinic receptor antagonist, caused only a slight blockade in the presser effect of THA. Simultaneous pretreatment with atropine and mecamylamine almost abolished the blood pressure effect of i.c.v. THA (25 mug). Haemorrhage increased plasma levels of adrenaline, noradrenaline, vasopressin and plasma renin activity. THA (25 mug, i.c.v.) administration caused additional increases in vasopressin and adrenaline levels but not of renin activity and noradrenaline levels. The reversal of hypotension by THA was greatly attenuated by administration of either prazosin, an al-adrenoceptor antagonist (0.5 mg/kg, i.v.) or by the vasopressin V-1 receptor antagonist [beta -mercapto-beta,beta -cyclopenta-methylenepropionyl(1), O-Me-Tyr(2)-Arg(8)]-vasopressin (10 mug/kg, i.v.). Pretreatment of rats with both prazosin and the vasopressin antagonist simultaneously completely inhibited the presser response. Intravenous administration of THA (1, 1.5 and 3 mg/kg) also reversed hypotension in rats. Atropine (10 mug, i.c.v.) greatly attenuated the presser response to THA (1.5 mg/kg, i.v.), while mecamylamine (50 mug, i.c.v.) failed to change the presser effect of THA. In anaesthetised haemorrhaged rats, THA (1.5 mg/kg, i.v.) increased blood pressure and survival time of the animals. These results show that centrally and peripherally injected THA reverses haemorrhagic hypotension and increases survival time in rats. Activation of central muscarinic and nicotinic receptors is involved in the presser response to i.c.v. THA. The presser effect of i.v. THA is solely mediated by central muscarinic receptors. Moreover, the increase in plasma adrenaline and vasopressin levels appears to be involved in the presser effect of THA. Copyright (C) 2001 S. Karger AG, Basel.