Yuzurihara Mitsutoshi, Ikarashi Yasushi, Noguchi Masamichi, Kase Yoshio, Takeda Shuichi, Aburada Masaki
Tsumura Research Institute, Medical Evaluation Laboratory, Ami-machi, Inashiki-gun, Ibaraki, Japan.
Urology. 2003 Nov;62(5):947-51. doi: 10.1016/s0090-4295(03)00587-9.
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 microg/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 CGRP8-37 (1000 microg/kg intravenously), a CGRP1 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 CGRP8-37 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.
为了评估降钙素基因相关肽(CGRP)在前列腺癌去势治疗后男性潮热发生中的作用,我们研究了CGRP对手术去势和药物去势雄性大鼠皮肤温度的影响。
在雄性大鼠双侧睾丸切除术后3周或皮下注射促性腺激素释放激素类似物(1.0mg/kg亮丙瑞林)2周后,静脉注射10μg/kg的CGRP及CGRP家族肽(肾上腺髓质素和胰淀素),每隔5分钟测量后爪皮肤温度变化,共测量120分钟。在注射CGRP前10分钟静脉注射CGRP1受体拮抗剂CGRP8 - 37(1000μg/kg),检测其对CGRP诱导反应的拮抗作用。在温度分析前14天,每天皮下注射睾酮(1.0mg/kg),评估睾酮替代对去势大鼠的影响。
与假手术组大鼠相比,CGRP(而非肾上腺髓质素和胰淀素)使手术或药物去势诱导的睾酮缺乏大鼠的皮肤温度升高更明显。差异具有统计学意义。去势大鼠中CGRP诱导的增强作用可通过用CGRP8 - 37预处理或补充睾酮来抑制。
CGRP是能使雄性大鼠皮肤温度升高的肽家族中最有效的肽。皮肤温度升高受去势导致的睾酮缺乏影响更大。这些结果表明CGRP参与了男性潮热的潜在机制。