Ukai M, Toyoshi T, Mizutani M, Sasaki Y, Kameyama T
Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Meijo University, Nagoya, Japan.
Nihon Shinkei Seishin Yakurigaku Zasshi. 1994 Jun;14(3):161-8.
The effects of [D-Ala2, NMePhe4, Gly-ol]enkephalin (DAMGO), a mu-selective opioid receptor agonist, [D-Ala2]deltorphin II (DELT) and [D-Pen2, L-Pen5]enkephalin (DPLPE), delta-selective opioid receptor agonists, on different behavioral responses were investigated in mice by multidimensional behavioral analyses. DAMGO (0.1 and/or 0.3 microgram) produced a marked increase in circling, rearing and grooming within 15-30 min after the start of behavioral measurements. DELT (0.3, 1.0 and/or 3.0 micrograms) produced a significant increase in linear locomotion and circling within 15-30 min after the start of behavioral measurements, whereas DPLPE (10.0 micrograms) increased only circling. The behavioral effects of DAMGO, DELT or DPLPE were almost completely antagonized by beta-funaltrexamine (2.5 and 5.0 micrograms) or naltrindole (3.0 and 10.0 mg/kg). These results suggest that opioid peptides selective for receptor types elicit different behavioral responses in mice. Moreover, the different behavioral effects between DPLPE and DELT may be due to the delta opioid receptor subtypes such as delta-1 and delta-2.
通过多维行为分析,研究了μ选择性阿片受体激动剂[D - Ala2,NMePhe4,Gly - ol]脑啡肽(DAMGO)、δ选择性阿片受体激动剂[D - Ala2]强啡肽II(DELT)和[D - Pen2,L - Pen5]脑啡肽(DPLPE)对小鼠不同行为反应的影响。在行为测量开始后的15 - 30分钟内,DAMGO(0.1微克和/或0.3微克)使转圈、直立和理毛行为显著增加。DELT(0.3微克、1.0微克和/或3.0微克)在行为测量开始后的15 - 30分钟内使直线运动和转圈行为显著增加,而DPLPE(10.0微克)仅增加了转圈行为。DAMGO、DELT或DPLPE的行为效应几乎完全被β - 芬太尼丁(2.5微克和5.0微克)或纳曲吲哚(3.0毫克/千克和10.0毫克/千克)拮抗。这些结果表明,对受体类型具有选择性的阿片肽在小鼠中引发不同的行为反应。此外,DPLPE和DELT之间不同的行为效应可能归因于δ阿片受体亚型,如δ - 1和δ - 2。