L. Groenink et al., NEUROENDOCRINE EFFECTS OF DIAZEPAM AND FLESINOXAN IN THE STRESS-INDUCED HYPERTHERMIA TEST IN MICE, Pharmacology, biochemistry and behavior, 54(1), 1996, pp. 249-254
In the stress-induced hyperthermia (SIH) paradigm in mice, both a benz
odiazepine receptor agonist, diazepam, and a 5-HT1A receptor agonist,
flesinoxan, reduced the stress-induced increase in rectal temperature.
The SIH procedure itself enhanced plasma ACTH and corticosterone leve
ls bur not plasma glucose levels. Diazepam (3, 6, and 12 mg/kg PO) did
neither affect basal plasma ACTH, corticosterone, or glucose levels,
nor did it suppress the stress-induced rises in these parameters. Fles
inoxan (1, 3, and 10 mg/kg PO) enhanced plasma ACTH and corticosterone
concentrations under nonstress conditions but did not affect the stre
ss-induced increases in ACTH and corticosterone secretion. No clear ef
fects of flesinoxan on plasma glucose levels were found. Our results i
ndicate that in mice the anxiolytic effects of diazepam and flesinoxan
in the SIH paradigm are not paralleled by a blockade of stress-induce
d increases in plasma ACTH, corticosterone, and glucose levels.