» Articles » PMID: 5789811

Steroid Potentiation of Responses to Sympathomimetic Amines in Aortic Strips

Overview
Journal Br J Pharmacol
Publisher Wiley
Specialty Pharmacology
Date 1969 Jul 1
PMID 5789811
Citations 28
Authors
Affiliations
Soon will be listed here.
Abstract

1. Responses to catecholamines (adrenaline, noradrenaline, nordefrine) were enhanced by 17beta-oestradiol, progesterone and desoxycorticosterone in untreated and reserpine pretreated aortic strips. Responses to tyramine, believed mediated via endogenous catecholamines, were enhanced only in untreated strips.2. Responses to sympathomimetic amines lacking the catechol nucleus (phenylephrine, synephrine, methoxamine) were potentiated inconsistently by the steroids and reserpine pretreatment reduced markedly the frequency of potentiated responses.3. Known inhibitors of catechol-O-methyl transferase (tropolone, U-0521, pyrogallol) potentiated responses to catecholamines and abolished the enhancing effects of the steroids-when the steroids were given first, there was no further increase in response to catecholamines on adding inhibitors of catechol-O-methyl transferase.4. Experiments with the oil-immersion technique, to eliminate diffusion of drug from the tissue, indicated that 17beta-oestradiol, progesterone and desoxycorticosterone decreased the rate at which aortic strips inactivated adrenaline by O-methylation.5. It is concluded that 17beta-oestradiol, progesterone and desoxycorticosterone potentiate responses to catecholamines in aortic strips by inhibiting a major mechanism for their inactivation.

Citing Articles

Organic cation transporter 3: A cellular mechanism underlying rapid, non-genomic glucocorticoid regulation of monoaminergic neurotransmission, physiology, and behavior.

Gasser P, Lowry C Horm Behav. 2018; 104:173-182.

PMID: 29738736 PMC: 7137088. DOI: 10.1016/j.yhbeh.2018.05.003.


Gender differences in microcirculation: observation using the hamster cheek pouch.

Panazzolo D, Silva L, Cyrino F, Sicuro F, Kraemer-Aguiar L, Bouskela E Clinics (Sao Paulo). 2014; 68(12):1537-42.

PMID: 24473512 PMC: 3840373. DOI: 10.6061/clinics/2013(12)10.


Monoamines and ovarian hormone-linked sexual and emotional changes: A review.

Janowsky D, Fann W, Davis J Arch Sex Behav. 2013; 1(3):205-18.

PMID: 24179066 DOI: 10.1007/BF01541683.


Historical studies of premenstrual tension up to 30 years ago: implications for future research.

Janowsky D, Rausch J, Davis J Curr Psychiatry Rep. 2002; 4(6):411-8.

PMID: 12441020 DOI: 10.1007/s11920-002-0068-8.


Premenstrual asthma: epidemiology, pathogenesis and treatment.

Tan K Drugs. 2001; 61(14):2079-86.

PMID: 11735634 DOI: 10.2165/00003495-200161140-00005.


References
1.
Kalsner S, Nickerson M . Effects of a haloalkylamine on responses to and disposition of sympathomimetic amines. Br J Pharmacol. 1969; 35(3):440-55. PMC: 1703368. DOI: 10.1111/j.1476-5381.1969.tb08285.x. View

2.
Wurtman R, Chu E, Axelrod J . Relation between the oestrous cycle and the binding of catecholamines in the rat uterus. Nature. 1963; 198:547-8. DOI: 10.1038/198547a0. View

3.
Belleau B, Burba J . Tropolones: a unique class of potent non-competitive inhibitors of S-adenosylmethionine-catechol methyltransferase. Biochim Biophys Acta. 1961; 54:195-6. DOI: 10.1016/0006-3002(61)90956-8. View

4.
Kalsner S, Nickerson M . Disposition of norepinephrine and epinephrine in vascular tissue, determined by the technique of oil immersion. J Pharmacol Exp Ther. 1969; 165(2):152-65. View

5.
Kalsner S, Nickerson M . A method for the study of mechanisms of drug disposition in smooth muscle. Can J Physiol Pharmacol. 1968; 46(5):719-30. DOI: 10.1139/y68-113. View