Involvement of calcitonin gene-related peptide in elevation of skin temperature in castrated male rats

To assess the involvement of calcitonin gene-related peptide (CGRP) in the occurrence of hot flashes in men after castration for treatment of prostate cancer, we investigated the effects of CGRP on skin temperature in surgically and medically castrated male rats. Changes in skin temperature of the h...

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Veröffentlicht in:Urology (Ridgewood, N.J.) N.J.), 2003-11, Vol.62 (5), p.947-951
Hauptverfasser: Yuzurihara, Mitsutoshi, Ikarashi, Yasushi, Noguchi, Masamichi, Kase, Yoshio, Takeda, Shuichi, Aburada, Masaki
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container_issue 5
container_start_page 947
container_title Urology (Ridgewood, N.J.)
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creator Yuzurihara, Mitsutoshi
Ikarashi, Yasushi
Noguchi, Masamichi
Kase, Yoshio
Takeda, Shuichi
Aburada, Masaki
description To assess the involvement of calcitonin gene-related peptide (CGRP) in the occurrence of hot flashes in men after castration for treatment of prostate cancer, we investigated the effects of CGRP on skin temperature in surgically and medically castrated male rats. Changes in skin temperature of the hind paws after intravenous injection of 10 μg/kg of CGRP and CGRP family peptides (adrenomedullin and amylin) were measured at 5-minute intervals for 120 minutes, 3 weeks after bilateral orchiectomy or 2 weeks after subcutaneous injection of a gonadotropin-releasing hormone analogue (1.0 mg/kg Leuplin) in male rats. Antagonism with CGRP 8-37 (1000 μg/kg intravenously), a CGRP 1 receptor antagonist, to the CGRP-induced response was examined by injecting it 10 minutes before injection of CGRP. The effect of testosterone replacement on castration was evaluated in each castrated rat by the administration of testosterone (1.0 mg/kg subcutaneously once a day) for 14 days before the day of the temperature analysis. CGRP, but not adrenomedullin and amylin, elevated the skin temperature in surgical or medical castration-induced testosterone-deficient rats more than in the sham-treated rats. The difference was statistically significant. The CGRP-induced potentiation in the castrated rats was inhibited by pretreating with CGRP 8-37 or by supplying testosterone. CGRP is the most potent peptide in a family that elevates the skin temperature in male rats. The elevation of the skin temperature was more affected by the testosterone deficiency resulting from castration. These results suggest that CGRP is involved in the mechanism underlying hot flashes in men.
doi_str_mv 10.1016/S0090-4295(03)00587-9
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Changes in skin temperature of the hind paws after intravenous injection of 10 μg/kg of CGRP and CGRP family peptides (adrenomedullin and amylin) were measured at 5-minute intervals for 120 minutes, 3 weeks after bilateral orchiectomy or 2 weeks after subcutaneous injection of a gonadotropin-releasing hormone analogue (1.0 mg/kg Leuplin) in male rats. Antagonism with CGRP 8-37 (1000 μg/kg intravenously), a CGRP 1 receptor antagonist, to the CGRP-induced response was examined by injecting it 10 minutes before injection of CGRP. The effect of testosterone replacement on castration was evaluated in each castrated rat by the administration of testosterone (1.0 mg/kg subcutaneously once a day) for 14 days before the day of the temperature analysis. CGRP, but not adrenomedullin and amylin, elevated the skin temperature in surgical or medical castration-induced testosterone-deficient rats more than in the sham-treated rats. The difference was statistically significant. 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Changes in skin temperature of the hind paws after intravenous injection of 10 μg/kg of CGRP and CGRP family peptides (adrenomedullin and amylin) were measured at 5-minute intervals for 120 minutes, 3 weeks after bilateral orchiectomy or 2 weeks after subcutaneous injection of a gonadotropin-releasing hormone analogue (1.0 mg/kg Leuplin) in male rats. Antagonism with CGRP 8-37 (1000 μg/kg intravenously), a CGRP 1 receptor antagonist, to the CGRP-induced response was examined by injecting it 10 minutes before injection of CGRP. The effect of testosterone replacement on castration was evaluated in each castrated rat by the administration of testosterone (1.0 mg/kg subcutaneously once a day) for 14 days before the day of the temperature analysis. CGRP, but not adrenomedullin and amylin, elevated the skin temperature in surgical or medical castration-induced testosterone-deficient rats more than in the sham-treated rats. The difference was statistically significant. The CGRP-induced potentiation in the castrated rats was inhibited by pretreating with CGRP 8-37 or by supplying testosterone. CGRP is the most potent peptide in a family that elevates the skin temperature in male rats. The elevation of the skin temperature was more affected by the testosterone deficiency resulting from castration. These results suggest that CGRP is involved in the mechanism underlying hot flashes in men.</abstract><cop>New York, NY</cop><pub>Elsevier Inc</pub><pmid>14624932</pmid><doi>10.1016/S0090-4295(03)00587-9</doi><tpages>5</tpages></addata></record>
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subjects Adrenomedullin
Amyloid - administration & dosage
Amyloid - pharmacology
Animals
Biological and medical sciences
Calcitonin Gene-Related Peptide - administration & dosage
Calcitonin Gene-Related Peptide - pharmacology
Calcitonin Gene-Related Peptide - physiology
Fundamental and applied biological sciences. Psychology
Gonadotropin-Releasing Hormone - antagonists & inhibitors
Hindlimb
Hormone Antagonists - pharmacology
Hormones and neuropeptides. Regulation
Hot Flashes - physiopathology
Hypothalamus. Hypophysis. Epiphysis. Urophysis
Injections, Intravenous
Islet Amyloid Polypeptide
Leuprolide - pharmacology
Male
Orchiectomy
Peptide Fragments - pharmacology
Peptides - administration & dosage
Peptides - pharmacology
Rats
Rats, Sprague-Dawley
Receptors, Calcitonin Gene-Related Peptide - drug effects
Skin Temperature - physiology
Testosterone - pharmacology
Vertebrates: endocrinology
title Involvement of calcitonin gene-related peptide in elevation of skin temperature in castrated male rats
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