Effect of pentoxifylline on α- and β-adrenoceptor sites in cerebral cortex, medial basal hypothalamus and pineal gland of the rat

The intraperitoneal injection of the methylxanthine derivative pentoxifylline [3,7-dimethyl-1-(5-oxo-hexyl)-xanthine] brought about, 3 hr later, a significant depression of α- and β-adrenoceptor sites in the cerebral cortex, and of β-adrenoceptor sites in medial basal hypothalamus and pineal gland,...

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Publicado: 1982
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rat
Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00283908_v21_n3_p243_Lowenstein
http://hdl.handle.net/20.500.12110/paper_00283908_v21_n3_p243_Lowenstein
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spelling paper:paper_00283908_v21_n3_p243_Lowenstein2023-06-08T14:55:09Z Effect of pentoxifylline on α- and β-adrenoceptor sites in cerebral cortex, medial basal hypothalamus and pineal gland of the rat adrenergic receptors binding studies cerebral cortex medial basal hypothalamus pentoxifylline [3,7-dimethyl-1-(5-oxo-hexyl)-xanthine], methylxanthines pineal gland superior cervical ganglion alpha adrenergic receptor beta adrenergic receptor dihydroergocryptine drug receptor pentoxifylline phentolamine propranolol radioisotope animal experiment brain cortex central nervous system dihydroalprenolol h 3 dihydroergocryptine h 3 hypothalamus pineal body rat Animal Binding Sites Cerebral Cortex Dihydroalprenolol Dihydroergotoxine Female Hypothalamus Pentoxifylline Pineal Gland Rats Rats, Inbred Strains Receptors, Adrenergic Receptors, Adrenergic, alpha Receptors, Adrenergic, beta Support, Non-U.S. Gov't Theobromine The intraperitoneal injection of the methylxanthine derivative pentoxifylline [3,7-dimethyl-1-(5-oxo-hexyl)-xanthine] brought about, 3 hr later, a significant depression of α- and β-adrenoceptor sites in the cerebral cortex, and of β-adrenoceptor sites in medial basal hypothalamus and pineal gland, (assessed from the specific binding of radioactive dihydroergocryptine and dihydroalprenolol respectively). The changes in the density of binding sites were not accompanied by significant modifications of the Kd′s. Sympathetic denervation of the pineal gland by superior cervical ganglionectomy (SCGx) abolished the changes of β-adrenoceptor number in the pineal caused by pentoxifylline. The increase of α-adrenoceptor sites in the hypothalamus brought about by ganglionectomy was not affected by injection of pentoxifylline. Pentoxifylline did not compete in vitro for radioligand binding to brain membranes. These results suggest that methylxanthines depress brain adrenoceptor sites acutely, probably by down-regulation of receptors following the increase in catecholamine release caused by injection of the drug. © 1982. 1982 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00283908_v21_n3_p243_Lowenstein http://hdl.handle.net/20.500.12110/paper_00283908_v21_n3_p243_Lowenstein
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic adrenergic receptors
binding studies
cerebral cortex
medial basal hypothalamus
pentoxifylline [3,7-dimethyl-1-(5-oxo-hexyl)-xanthine], methylxanthines
pineal gland
superior cervical ganglion
alpha adrenergic receptor
beta adrenergic receptor
dihydroergocryptine
drug receptor
pentoxifylline
phentolamine
propranolol
radioisotope
animal experiment
brain cortex
central nervous system
dihydroalprenolol h 3
dihydroergocryptine h 3
hypothalamus
pineal body
rat
Animal
Binding Sites
Cerebral Cortex
Dihydroalprenolol
Dihydroergotoxine
Female
Hypothalamus
Pentoxifylline
Pineal Gland
Rats
Rats, Inbred Strains
Receptors, Adrenergic
Receptors, Adrenergic, alpha
Receptors, Adrenergic, beta
Support, Non-U.S. Gov't
Theobromine
spellingShingle adrenergic receptors
binding studies
cerebral cortex
medial basal hypothalamus
pentoxifylline [3,7-dimethyl-1-(5-oxo-hexyl)-xanthine], methylxanthines
pineal gland
superior cervical ganglion
alpha adrenergic receptor
beta adrenergic receptor
dihydroergocryptine
drug receptor
pentoxifylline
phentolamine
propranolol
radioisotope
animal experiment
brain cortex
central nervous system
dihydroalprenolol h 3
dihydroergocryptine h 3
hypothalamus
pineal body
rat
Animal
Binding Sites
Cerebral Cortex
Dihydroalprenolol
Dihydroergotoxine
Female
Hypothalamus
Pentoxifylline
Pineal Gland
Rats
Rats, Inbred Strains
Receptors, Adrenergic
Receptors, Adrenergic, alpha
Receptors, Adrenergic, beta
Support, Non-U.S. Gov't
Theobromine
Effect of pentoxifylline on α- and β-adrenoceptor sites in cerebral cortex, medial basal hypothalamus and pineal gland of the rat
topic_facet adrenergic receptors
binding studies
cerebral cortex
medial basal hypothalamus
pentoxifylline [3,7-dimethyl-1-(5-oxo-hexyl)-xanthine], methylxanthines
pineal gland
superior cervical ganglion
alpha adrenergic receptor
beta adrenergic receptor
dihydroergocryptine
drug receptor
pentoxifylline
phentolamine
propranolol
radioisotope
animal experiment
brain cortex
central nervous system
dihydroalprenolol h 3
dihydroergocryptine h 3
hypothalamus
pineal body
rat
Animal
Binding Sites
Cerebral Cortex
Dihydroalprenolol
Dihydroergotoxine
Female
Hypothalamus
Pentoxifylline
Pineal Gland
Rats
Rats, Inbred Strains
Receptors, Adrenergic
Receptors, Adrenergic, alpha
Receptors, Adrenergic, beta
Support, Non-U.S. Gov't
Theobromine
description The intraperitoneal injection of the methylxanthine derivative pentoxifylline [3,7-dimethyl-1-(5-oxo-hexyl)-xanthine] brought about, 3 hr later, a significant depression of α- and β-adrenoceptor sites in the cerebral cortex, and of β-adrenoceptor sites in medial basal hypothalamus and pineal gland, (assessed from the specific binding of radioactive dihydroergocryptine and dihydroalprenolol respectively). The changes in the density of binding sites were not accompanied by significant modifications of the Kd′s. Sympathetic denervation of the pineal gland by superior cervical ganglionectomy (SCGx) abolished the changes of β-adrenoceptor number in the pineal caused by pentoxifylline. The increase of α-adrenoceptor sites in the hypothalamus brought about by ganglionectomy was not affected by injection of pentoxifylline. Pentoxifylline did not compete in vitro for radioligand binding to brain membranes. These results suggest that methylxanthines depress brain adrenoceptor sites acutely, probably by down-regulation of receptors following the increase in catecholamine release caused by injection of the drug. © 1982.
title Effect of pentoxifylline on α- and β-adrenoceptor sites in cerebral cortex, medial basal hypothalamus and pineal gland of the rat
title_short Effect of pentoxifylline on α- and β-adrenoceptor sites in cerebral cortex, medial basal hypothalamus and pineal gland of the rat
title_full Effect of pentoxifylline on α- and β-adrenoceptor sites in cerebral cortex, medial basal hypothalamus and pineal gland of the rat
title_fullStr Effect of pentoxifylline on α- and β-adrenoceptor sites in cerebral cortex, medial basal hypothalamus and pineal gland of the rat
title_full_unstemmed Effect of pentoxifylline on α- and β-adrenoceptor sites in cerebral cortex, medial basal hypothalamus and pineal gland of the rat
title_sort effect of pentoxifylline on α- and β-adrenoceptor sites in cerebral cortex, medial basal hypothalamus and pineal gland of the rat
publishDate 1982
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00283908_v21_n3_p243_Lowenstein
http://hdl.handle.net/20.500.12110/paper_00283908_v21_n3_p243_Lowenstein
_version_ 1768542877214834688