Rawls Scott M, Amin Manisha, Zisk Jacob
Department of Pharmaceutical Sciences, Temple University School of Pharmacy, Philadelphia, PA 19140, USA.
Brain Res. 2007 May 25;1147:89-94. doi: 10.1016/j.brainres.2006.09.047. Epub 2007 Mar 21.
The present study investigated the effect of agmatine on morphine-evoked hyperthermia in rats. Morphine (4 mg/kg, s.c.) produced hyperthermia by activating mu opioid receptors. Agmatine (10 and 50 mg/kg, i.p.) was ineffective. For combined administration, agmatine decreased morphine-evoked hyperthermia. The effect was prevented by idazoxan (5 mg/kg, i.p.), an imidazoline/alpha(2)-adrenoeceptor receptor antagonist. Yohimbine, an alpha(2)-adrenoeceptor antagonist, did not prevent the attenuation of morphine-evoked hyperthermia by agmatine. The present data provide pharmacological evidence that agmatine blocks the hyperthermic effect of morphine by activating imidazoline receptors.
本研究调查了胍丁胺对大鼠吗啡诱发体温过高的影响。吗啡(4毫克/千克,皮下注射)通过激活μ阿片受体产生体温过高。胍丁胺(10和50毫克/千克,腹腔注射)无效。联合给药时,胍丁胺可降低吗啡诱发的体温过高。该作用被咪唑啉/α2-肾上腺素能受体拮抗剂咪唑克生(5毫克/千克,腹腔注射)阻断。α2-肾上腺素能受体拮抗剂育亨宾不能阻断胍丁胺对吗啡诱发体温过高的减弱作用。目前的数据提供了药理学证据,表明胍丁胺通过激活咪唑啉受体来阻断吗啡的体温过高作用。