The effect of 8-OH-DPAT on temperature in the rat and its modification by chronic antidepressant treatments
- PMID: 2971978
- DOI: 10.1016/0091-3057(88)90479-0
The effect of 8-OH-DPAT on temperature in the rat and its modification by chronic antidepressant treatments
Abstract
Administration of 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT) to rats produced a dose-dependent hypothermia. Pretreatment with the receptor antagonist methiothepin abolished this effect, and pretreatment with haloperidol, propranolol and pindolol partially attenuated it, although methiothepin and pindolol had hyperthermic actions of their own. Other receptor antagonists including ritanserin, naloxone, clonidine, phenoxybenzamine and metergoline did not significantly modify the response elicited by subsequent 8-OH-DPAT challenge. In antidepressant studies, chronic treatment (22 days) with clorgyline attenuated the hypothermic response to 8-OH-DPAT, whereas similar duration of treatment with the tricyclics clomipramine and imipramine did not significantly modify it. Also, acute treatment for three days with each of the antidepressants did not modify 8-OH-DPAT-induced hypothermia. We conclude that rat rectal temperature can be a useful model to help assess the functional state of serotonergic mechanisms, including the adaptational changes induced by long-term antidepressant treatment.
Similar articles
-
The pharmacology of the hypothermic response in mice to 8-hydroxy-2-(di-n-propylamino)tetralin (8-OH-DPAT). A model of presynaptic 5-HT1 function.Neuropharmacology. 1985 Dec;24(12):1187-94. doi: 10.1016/0028-3908(85)90153-4. Neuropharmacology. 1985. PMID: 2869435
-
Attenuation by electroconvulsive shock and antidepressant drugs of the 5-HT1A receptor-mediated hypothermia and serotonin syndrome produced by 8-OH-DPAT in the rat.Psychopharmacology (Berl). 1987;91(4):500-5. doi: 10.1007/BF00216018. Psychopharmacology (Berl). 1987. PMID: 2954178
-
The behavioural, but not the hypothermic or corticosterone, response to 8-hydroxy-2-(DI-n-propylamino)-tetralin, is antagonized by NAN-190 in the rat.Neuropharmacology. 1990 Jun;29(6):521-6. doi: 10.1016/0028-3908(90)90063-w. Neuropharmacology. 1990. PMID: 2143565
-
Pharmacological characterization of 8-OH-DPAT-induced inhibition of rat hippocampal 5-HT release in vivo as measured by microdialysis.Br J Pharmacol. 1989 Nov;98(3):989-97. doi: 10.1111/j.1476-5381.1989.tb14630.x. Br J Pharmacol. 1989. PMID: 2574066 Free PMC article.
-
Food intake, neuroendocrine and temperature effects of 8-OHDPAT in the rat.Eur J Pharmacol. 1988 Feb 9;146(2-3):253-9. doi: 10.1016/0014-2999(88)90300-7. Eur J Pharmacol. 1988. PMID: 2967188
Cited by
-
Fluoxetine decreases brain temperature and REM sleep in Syrian hamsters.Psychopharmacology (Berl). 1992;106(3):321-9. doi: 10.1007/BF02245412. Psychopharmacology (Berl). 1992. PMID: 1570377
-
Evidence for 5-hydroxytryptamine1A receptor involvement in the control of prolactin secretion in man.Psychopharmacology (Berl). 1995 Jun;119(3):311-4. doi: 10.1007/BF02246297. Psychopharmacology (Berl). 1995. PMID: 7675967 Clinical Trial.
-
Long-term fluoxetine treatment decreases 5-HT1A receptor responsivity in obsessive-compulsive disorder.Psychopharmacology (Berl). 1991;105(3):415-20. doi: 10.1007/BF02244438. Psychopharmacology (Berl). 1991. PMID: 1686817 Clinical Trial.
-
Serotonergic modulation of the rat pup ultrasonic isolation call: studies with 5HT1 and 5HT2 subtype-selective agonists and antagonists.Psychopharmacology (Berl). 1991;105(4):513-20. doi: 10.1007/BF02244372. Psychopharmacology (Berl). 1991. PMID: 1771219
-
Systemic serotonin inhibits brown adipose tissue sympathetic nerve activity via a GABA input to the dorsomedial hypothalamus, not via 5HT1A receptor activation in raphe pallidus.Acta Physiol (Oxf). 2020 Mar;228(3):e13401. doi: 10.1111/apha.13401. Epub 2019 Nov 1. Acta Physiol (Oxf). 2020. PMID: 31599481 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical