Subsensitivity of human beta-adrenergic adenylate cyclase after salbutamol treatment of depression
- PMID: 6275441
- DOI: 10.1007/BF00432181
Subsensitivity of human beta-adrenergic adenylate cyclase after salbutamol treatment of depression
Abstract
Although numerous studies have suggested that depression may be associated with a reduction in synaptic noradrenaline in the brain, direct beta-adrenergic receptor agonist have only recently been tested in the treatement of depression. Moreover, newer theories of antidepressant action suggest that a reduction in beta-adrenergic receptor sensitivity is a better correlate of antidepressant treatment than noradrenaline turnover changes. Eleven depressed patients were treated with salbutamol, a beta-2-adrenergic agonist, and beta-2-adrenergic receptor sensitivity was evaluated before, during, and after treatment. beta-Adrenergic receptor sensitivity was evaluated by measuring the plasma cyclic AMP increase after an IV dose of salbutamol. The beta-adrenergic agonist exhibited antidepressant efficacy and induced subsensitivity of the beta-adrenergic adenylate cyclase with a time course paralleling the antidepressant effects. The results support the concept that receptor sensitivity changes occur during antidepressant therapy.
Similar articles
-
Receptors, adenylate cyclase, depression, and lithium.Biol Psychiatry. 1981 Apr;16(4):333-50. Biol Psychiatry. 1981. PMID: 6261845
-
Lithium does not prevent agonist-induced subsensitivity of human adenylate cyclase.Biol Psychiatry. 1982 Mar;17(3):343-50. Biol Psychiatry. 1982. PMID: 6282346
-
Adenylate cyclase and the search for new compounds with the clinical profile of lithium.Pharmacopsychiatry. 1984 Jan;17(1):9-15. doi: 10.1055/s-2007-1017400. Pharmacopsychiatry. 1984. PMID: 6324249
-
Regulation of recognition and action function of the norepinephrine (NE) receptor-coupled adenylate cyclase system in brain: implications for the therapy of depression.Neuropharmacology. 1983 Mar;22(3 Spec No):425-31. doi: 10.1016/0028-3908(83)90192-2. Neuropharmacology. 1983. PMID: 6304560 Review. No abstract available.
-
The cyclic AMP second messenger system in man: the effects of heredity, hormones, drugs, aluminum, age and disease on signal amplification.Prog Neuropsychopharmacol Biol Psychiatry. 1986;10(3-5):323-53. doi: 10.1016/0278-5846(86)90011-4. Prog Neuropsychopharmacol Biol Psychiatry. 1986. PMID: 3025924 Review.
Cited by
-
Lesions of the serotonergic system impair the facilitation of but not the tolerance to the effects of chronic clenbuterol administration.Psychopharmacology (Berl). 1987;91(4):496-9. doi: 10.1007/BF00216017. Psychopharmacology (Berl). 1987. PMID: 2438713
-
The effect of chronic bromocriptine and L-dopa on spiperone binding and apomorphine-induced stereotypy.Psychopharmacology (Berl). 1982;78(1):81-4. doi: 10.1007/BF00470594. Psychopharmacology (Berl). 1982. PMID: 6815701
-
beta-Adrenoceptor agonists enhance 5-hydroxytryptamine-mediated behavioural responses.Br J Pharmacol. 1982 Jun;76(2):265-70. doi: 10.1111/j.1476-5381.1982.tb09216.x. Br J Pharmacol. 1982. PMID: 6124294 Free PMC article.
-
Adverse reactions to beta 2-agonist bronchodilators.Med Toxicol. 1986 Jul-Aug;1(4):286-99. doi: 10.1007/BF03259844. Med Toxicol. 1986. PMID: 2878344 Review.
-
Effects of long-term administration of antidepressants and neuroleptics on receptors in the central nervous system.Cell Mol Neurobiol. 1989 Mar;9(1):1-44. doi: 10.1007/BF00711441. Cell Mol Neurobiol. 1989. PMID: 2565769 Free PMC article. Review.
References
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources