α‐Adrenoceptor stimulated lymphocytes trigger the mechanical response of vas deferens: participation of arachidonic acid metabolites

Normal human lymphocytes (L) (8 × 105 ml−1) incubated with methoxamine (Me) (1 × 10−7 M) (Me‐L) triggered the mchanical response of the isolated vas deferens of the rat. L or Me alone did not modify this contractile activity at the concentrations cited above. Me alone (10−6 to 10−3 M) increased the...

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Publicado: 1984
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00071188_v82_n4_p863_Borda
http://hdl.handle.net/20.500.12110/paper_00071188_v82_n4_p863_Borda
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spelling paper:paper_00071188_v82_n4_p863_Borda2023-06-08T14:31:38Z α‐Adrenoceptor stimulated lymphocytes trigger the mechanical response of vas deferens: participation of arachidonic acid metabolites 7 [3 (4 acetyl 3 hydroxy 2 propylphenoxy) 2 hydroxypropoxy] 4 oxo 8 propyl 4h 1 benzopyran 2 carboxylic acid acetylsalicylic acid alpha adrenergic receptor arachidonic acid indometacin lipoxygenase inhibitor methoxamine nordihydroguaiaretic acid phentolamine prazosin prostaglandin synthase inhibitor yohimbine animal cell blood and hemopoietic system drug efficacy human human cell lymphatic system lymphocyte male genital system muscle nonhuman normal human rat smooth muscle contractility vas deferens Adrenergic alpha-Agonists Adrenergic alpha-Antagonists Animals Arachidonic Acid Arachidonic Acids Humans Lipoxygenase Inhibitors Lymphocytes Male Methoxamine Muscle Contraction Muscle, Smooth Rats Time Factors Vas Deferens Normal human lymphocytes (L) (8 × 105 ml−1) incubated with methoxamine (Me) (1 × 10−7 M) (Me‐L) triggered the mchanical response of the isolated vas deferens of the rat. L or Me alone did not modify this contractile activity at the concentrations cited above. Me alone (10−6 to 10−3 M) increased the tension of the vas. In the presence of L (8 × 105 ml−1) the dose‐response curve to Me shifted to the left and the efficacy of Me was enhanced. Inhibitors of α1‐adrenoceptors completely blocked the reaction between Me and L while drugs that block α1 and α2‐adrenoceptors reduced the reaction between Me‐L and the vas deferens. Direct contact of Me‐L with the assay organ was not necessary. Cell‐free supernatants of L exposed to Me (Me‐L supernatants) elicited the reaction in the same way as Me‐L. This effect required the continuous presence of Me since dialyzed Me‐L supernatants were inactive. Inhibitors of lipoxygenase(s) completely blocked the positive inotropic effect of Me‐L or of Me‐L supernatants. Inhibitors of cyclo‐oxygenase potentiated this effect. These results suggest that Me reacts with α1‐adrenoceptors of L. From this reaction, soluble factors are released that potentiate the α‐adrenoceptor stimulatory effect of Me on the vas deferens as a consequence of the release of oxidative products of the lipoxygenase/s pathway of arachidonic acid. 1984 British Pharmacological Society 1984 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00071188_v82_n4_p863_Borda http://hdl.handle.net/20.500.12110/paper_00071188_v82_n4_p863_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 7 [3 (4 acetyl 3 hydroxy 2 propylphenoxy) 2 hydroxypropoxy] 4 oxo 8 propyl 4h 1 benzopyran 2 carboxylic acid
acetylsalicylic acid
alpha adrenergic receptor
arachidonic acid
indometacin
lipoxygenase inhibitor
methoxamine
nordihydroguaiaretic acid
phentolamine
prazosin
prostaglandin synthase inhibitor
yohimbine
animal cell
blood and hemopoietic system
drug efficacy
human
human cell
lymphatic system
lymphocyte
male genital system
muscle
nonhuman
normal human
rat
smooth muscle contractility
vas deferens
Adrenergic alpha-Agonists
Adrenergic alpha-Antagonists
Animals
Arachidonic Acid
Arachidonic Acids
Humans
Lipoxygenase Inhibitors
Lymphocytes
Male
Methoxamine
Muscle Contraction
Muscle, Smooth
Rats
Time Factors
Vas Deferens
spellingShingle 7 [3 (4 acetyl 3 hydroxy 2 propylphenoxy) 2 hydroxypropoxy] 4 oxo 8 propyl 4h 1 benzopyran 2 carboxylic acid
acetylsalicylic acid
alpha adrenergic receptor
arachidonic acid
indometacin
lipoxygenase inhibitor
methoxamine
nordihydroguaiaretic acid
phentolamine
prazosin
prostaglandin synthase inhibitor
yohimbine
animal cell
blood and hemopoietic system
drug efficacy
human
human cell
lymphatic system
lymphocyte
male genital system
muscle
nonhuman
normal human
rat
smooth muscle contractility
vas deferens
Adrenergic alpha-Agonists
Adrenergic alpha-Antagonists
Animals
Arachidonic Acid
Arachidonic Acids
Humans
Lipoxygenase Inhibitors
Lymphocytes
Male
Methoxamine
Muscle Contraction
Muscle, Smooth
Rats
Time Factors
Vas Deferens
α‐Adrenoceptor stimulated lymphocytes trigger the mechanical response of vas deferens: participation of arachidonic acid metabolites
topic_facet 7 [3 (4 acetyl 3 hydroxy 2 propylphenoxy) 2 hydroxypropoxy] 4 oxo 8 propyl 4h 1 benzopyran 2 carboxylic acid
acetylsalicylic acid
alpha adrenergic receptor
arachidonic acid
indometacin
lipoxygenase inhibitor
methoxamine
nordihydroguaiaretic acid
phentolamine
prazosin
prostaglandin synthase inhibitor
yohimbine
animal cell
blood and hemopoietic system
drug efficacy
human
human cell
lymphatic system
lymphocyte
male genital system
muscle
nonhuman
normal human
rat
smooth muscle contractility
vas deferens
Adrenergic alpha-Agonists
Adrenergic alpha-Antagonists
Animals
Arachidonic Acid
Arachidonic Acids
Humans
Lipoxygenase Inhibitors
Lymphocytes
Male
Methoxamine
Muscle Contraction
Muscle, Smooth
Rats
Time Factors
Vas Deferens
description Normal human lymphocytes (L) (8 × 105 ml−1) incubated with methoxamine (Me) (1 × 10−7 M) (Me‐L) triggered the mchanical response of the isolated vas deferens of the rat. L or Me alone did not modify this contractile activity at the concentrations cited above. Me alone (10−6 to 10−3 M) increased the tension of the vas. In the presence of L (8 × 105 ml−1) the dose‐response curve to Me shifted to the left and the efficacy of Me was enhanced. Inhibitors of α1‐adrenoceptors completely blocked the reaction between Me and L while drugs that block α1 and α2‐adrenoceptors reduced the reaction between Me‐L and the vas deferens. Direct contact of Me‐L with the assay organ was not necessary. Cell‐free supernatants of L exposed to Me (Me‐L supernatants) elicited the reaction in the same way as Me‐L. This effect required the continuous presence of Me since dialyzed Me‐L supernatants were inactive. Inhibitors of lipoxygenase(s) completely blocked the positive inotropic effect of Me‐L or of Me‐L supernatants. Inhibitors of cyclo‐oxygenase potentiated this effect. These results suggest that Me reacts with α1‐adrenoceptors of L. From this reaction, soluble factors are released that potentiate the α‐adrenoceptor stimulatory effect of Me on the vas deferens as a consequence of the release of oxidative products of the lipoxygenase/s pathway of arachidonic acid. 1984 British Pharmacological Society
title α‐Adrenoceptor stimulated lymphocytes trigger the mechanical response of vas deferens: participation of arachidonic acid metabolites
title_short α‐Adrenoceptor stimulated lymphocytes trigger the mechanical response of vas deferens: participation of arachidonic acid metabolites
title_full α‐Adrenoceptor stimulated lymphocytes trigger the mechanical response of vas deferens: participation of arachidonic acid metabolites
title_fullStr α‐Adrenoceptor stimulated lymphocytes trigger the mechanical response of vas deferens: participation of arachidonic acid metabolites
title_full_unstemmed α‐Adrenoceptor stimulated lymphocytes trigger the mechanical response of vas deferens: participation of arachidonic acid metabolites
title_sort α‐adrenoceptor stimulated lymphocytes trigger the mechanical response of vas deferens: participation of arachidonic acid metabolites
publishDate 1984
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_00071188_v82_n4_p863_Borda
http://hdl.handle.net/20.500.12110/paper_00071188_v82_n4_p863_Borda
_version_ 1768546141356425216