Alpha adrenergic stimulation modified prostaglandins release in vas deferens

Methoxamine enhanced contractions of mouse vasa deferentia through alpha adrenoceptor stimulation. Additionally, the generation of PGF-like material by the tissue was increased by methoxamine, whereas that of PGE-like material was decreased. The effects of methoxamine on prostaglandin output (stimul...

Descripción completa

Guardado en:
Detalles Bibliográficos
Publicado: 1983
Materias:
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00906980_v26_n5_p701_Borda
http://hdl.handle.net/20.500.12110/paper_00906980_v26_n5_p701_Borda
Aporte de:
id paper:paper_00906980_v26_n5_p701_Borda
record_format dspace
spelling paper:paper_00906980_v26_n5_p701_Borda2023-06-08T15:07:56Z Alpha adrenergic stimulation modified prostaglandins release in vas deferens acetylsalicylic acid alpha adrenergic receptor indometacin methoxamine phenoxybenzamine prostaglandin prostaglandin e2 prostaglandin f2 alpha trometamol yohimbine animal cell autonomic nervous system drug efficacy male genital system mouse nonhuman sympathetic nerve vas deferens Animal Aspirin Cyclooxygenase Inhibitors Indomethacin Male Methoxamine Mice Muscle Contraction Phenoxybenzamine Prostaglandins E Prostaglandins F Receptors, Adrenergic, alpha Support, Non-U.S. Gov't Vas Deferens Yohimbine Methoxamine enhanced contractions of mouse vasa deferentia through alpha adrenoceptor stimulation. Additionally, the generation of PGF-like material by the tissue was increased by methoxamine, whereas that of PGE-like material was decreased. The effects of methoxamine on prostaglandin output (stimulation and depression) were antagonized by yohimbine and phenoxybenzamine. Moreover, the stimulating influence of methoxamine on the contractile activity of the preparations was attenuated by the prostaglandin synthesis inhibitors indomethacin and acetylsalicylic acid. The results suggest that methoxamine is able to modify prostaglandin synthesis and output in mouse vasa deferentia, probably through an alpha adrenergic mediated mechanism coupled to the prostaglandin synthesizing system. The fact that indomethacin and acetylsalicylic acid blocked alpha stimulatory responses to methoxamine, suggest a modulatory role for endogenous prostaglandins. Since methoxamine increased PGF levels, this prostaglandin might potentiate the contractile influence of methoxamine. © 1983. 1983 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00906980_v26_n5_p701_Borda http://hdl.handle.net/20.500.12110/paper_00906980_v26_n5_p701_Borda
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic acetylsalicylic acid
alpha adrenergic receptor
indometacin
methoxamine
phenoxybenzamine
prostaglandin
prostaglandin e2
prostaglandin f2 alpha trometamol
yohimbine
animal cell
autonomic nervous system
drug efficacy
male genital system
mouse
nonhuman
sympathetic nerve
vas deferens
Animal
Aspirin
Cyclooxygenase Inhibitors
Indomethacin
Male
Methoxamine
Mice
Muscle Contraction
Phenoxybenzamine
Prostaglandins E
Prostaglandins F
Receptors, Adrenergic, alpha
Support, Non-U.S. Gov't
Vas Deferens
Yohimbine
spellingShingle acetylsalicylic acid
alpha adrenergic receptor
indometacin
methoxamine
phenoxybenzamine
prostaglandin
prostaglandin e2
prostaglandin f2 alpha trometamol
yohimbine
animal cell
autonomic nervous system
drug efficacy
male genital system
mouse
nonhuman
sympathetic nerve
vas deferens
Animal
Aspirin
Cyclooxygenase Inhibitors
Indomethacin
Male
Methoxamine
Mice
Muscle Contraction
Phenoxybenzamine
Prostaglandins E
Prostaglandins F
Receptors, Adrenergic, alpha
Support, Non-U.S. Gov't
Vas Deferens
Yohimbine
Alpha adrenergic stimulation modified prostaglandins release in vas deferens
topic_facet acetylsalicylic acid
alpha adrenergic receptor
indometacin
methoxamine
phenoxybenzamine
prostaglandin
prostaglandin e2
prostaglandin f2 alpha trometamol
yohimbine
animal cell
autonomic nervous system
drug efficacy
male genital system
mouse
nonhuman
sympathetic nerve
vas deferens
Animal
Aspirin
Cyclooxygenase Inhibitors
Indomethacin
Male
Methoxamine
Mice
Muscle Contraction
Phenoxybenzamine
Prostaglandins E
Prostaglandins F
Receptors, Adrenergic, alpha
Support, Non-U.S. Gov't
Vas Deferens
Yohimbine
description Methoxamine enhanced contractions of mouse vasa deferentia through alpha adrenoceptor stimulation. Additionally, the generation of PGF-like material by the tissue was increased by methoxamine, whereas that of PGE-like material was decreased. The effects of methoxamine on prostaglandin output (stimulation and depression) were antagonized by yohimbine and phenoxybenzamine. Moreover, the stimulating influence of methoxamine on the contractile activity of the preparations was attenuated by the prostaglandin synthesis inhibitors indomethacin and acetylsalicylic acid. The results suggest that methoxamine is able to modify prostaglandin synthesis and output in mouse vasa deferentia, probably through an alpha adrenergic mediated mechanism coupled to the prostaglandin synthesizing system. The fact that indomethacin and acetylsalicylic acid blocked alpha stimulatory responses to methoxamine, suggest a modulatory role for endogenous prostaglandins. Since methoxamine increased PGF levels, this prostaglandin might potentiate the contractile influence of methoxamine. © 1983.
title Alpha adrenergic stimulation modified prostaglandins release in vas deferens
title_short Alpha adrenergic stimulation modified prostaglandins release in vas deferens
title_full Alpha adrenergic stimulation modified prostaglandins release in vas deferens
title_fullStr Alpha adrenergic stimulation modified prostaglandins release in vas deferens
title_full_unstemmed Alpha adrenergic stimulation modified prostaglandins release in vas deferens
title_sort alpha adrenergic stimulation modified prostaglandins release in vas deferens
publishDate 1983
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00906980_v26_n5_p701_Borda
http://hdl.handle.net/20.500.12110/paper_00906980_v26_n5_p701_Borda
_version_ 1768543172791631872