Effect of psychotomimetics and some putative anxiolytics on stress-induced hyperthermia |
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Authors: | A. Lecci F. Borsini L. Gragnani G. Volterra A. Meli |
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Affiliation: | (1) Present address: Pharmacological Research Department, A. Menarini Pharmaceuticals, Firenze, Italy;(2) Present address: Istituto De Angeli, via Serio 15, 1-20139 Milano, Italy |
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Abstract: | Summary Stress-induced hyperthermia (SIH), which is seen in the last mice removed from the cage, is a novel animal model sensitive to anxiolytic drugs. SIH is antagonized by CL 218872 (25 and 50 mg/kg, os), by tracazolate (5 and 7.5 mg/kg, ip) and by 2-AP-5 (50 and 100 mg/kg, ip). At higher dose, CL 218872 (100 mg/kg, os) and tracazolate (12.5 mg/kg, ip) lose their activity.PK 9084 (5–40 mg/kg, ip) and CGS 9896 (2–20 mg/kg, both ip and os) were also ineffective in preventing SIH. The anti-hyperthermic effect of CL 218872 (25 mg/kg) and tracazolate (7.5 mg/kg) was blocked by the benzodiazepine antagonist Ro 15–1788 (15 mg/kg). CGS 9896 (10 mg/kg, os) also reversed the effect of CL 218872 (25 mg/kg) on SIH.Differently from anxiolytics, MK-801 (0.5–1 mg/kg, os), PCP (2.5 mg/kg, ip) and d-amphetamine (10 mg/kg, ip) evoked hyperthermia in the first set of mice and prevented a further stress-induced rise of body temperature in the last set of mice. |
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Keywords: | 2-AP-5 CGS9896 CL218872 d-amphetamine MK-801 PCP RO 15-1788 tracazolate temperature stress |
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