Murahata Yusuke, Yamamoto Asami, Miki Yuya, Hikasa Yoshiaki
Laboratory of Veterinary Internal Medicine, Joint Department of Veterinary Medicine, Faculty of Agriculture, Tottori University, 4-101 Koyama-Minami, Tottori 680-8553, Japan.
J Vet Med Sci. 2014 Mar 1;76(2):173-82. doi: 10.1292/jvms.13-0398. Epub 2013 Oct 8.
This study aimed to investigate and compare the antagonistic effects of atipamezole, yohimbine and prazosin on medetomidine-induced diuresis in healthy cats. Five cats were repeatedly used in each of the 9 groups. One group was not medicated. Cats in the other groups received 40 µg/kg medetomidine intramuscularly and saline (as the control), 160 µg/kg prazosin, or 40, 160 or 480 µg/kg atipamezole or yohimbine intravenously 0.5 hr later. Volume, pH and specific gravity of urine; plasma arginine vasopressin (AVP) level; and creatinine, osmolality and electrolyte levels in both urine and plasma were measured. Both atipamezole and yohimbine, but not prazosin, antagonized medetomidine-induced diuresis. The antidiuretic effect of atipamezole was more potent than that of yohimbine, but was not dose dependent, in contrast to the effect of yohimbine at the tested doses. Both atipamezole and yohimbine reversed medetomidine-induced decreases in both urine specific gravity and osmolality and increases in plasma osmolality and free-water clearance. Antidiuresis of either atipamezole or yohimbine was not related to the area under the curve for AVP level, although the highest dose of both atipamezole and yohimbine initially and temporarily increased plasma AVP levels, suggesting that this may partly influence the antidiuretic effects of both agents. The diuretic effect of medetomidine in cats may be mediated by α2-adrenoceptors, but not α1-adrenoceptors. Atipamezole and yohimbine can be used as antagonistic agents against medetomidine-induced diuresis in healthy cats.
本研究旨在调查并比较阿替美唑、育亨宾和哌唑嗪对健康猫体内美托咪定诱导的利尿作用的拮抗效果。9个组每组均重复使用5只猫。一组不给予药物治疗。其他组的猫肌肉注射40 µg/kg美托咪定和生理盐水(作为对照),0.5小时后静脉注射160 µg/kg哌唑嗪,或40、160或480 µg/kg阿替美唑或育亨宾。测量尿液的体积、pH值和比重;血浆精氨酸加压素(AVP)水平;以及尿液和血浆中的肌酐、渗透压和电解质水平。阿替美唑和育亨宾均可拮抗美托咪定诱导的利尿作用,而哌唑嗪则不能。与测试剂量下育亨宾的作用相反,阿替美唑的抗利尿作用比育亨宾更强,但不具有剂量依赖性。阿替美唑和育亨宾均可逆转美托咪定诱导的尿比重和渗透压降低以及血浆渗透压和自由水清除率增加。尽管阿替美唑和育亨宾的最高剂量最初会暂时增加血浆AVP水平,但阿替美唑或育亨宾的抗利尿作用均与AVP水平曲线下面积无关,这表明这可能部分影响了两种药物的抗利尿作用。美托咪定对猫的利尿作用可能由α2肾上腺素能受体介导,而非α1肾上腺素能受体。阿替美唑和育亨宾可作为健康猫体内美托咪定诱导利尿作用的拮抗药。