Ukai M, Toyoshi T, Kameyama T
Department of Chemical Pharmacology, Faculty of Pharmaceutical Sciences, Meijo University, Nagoya, Japan.
Pharmacol Biochem Behav. 1992 Aug;42(4):755-9. doi: 10.1016/0091-3057(92)90025-b.
The effects of dynorphin A(1-13) on the D1 dopamine agonist SK&F 38393- and the D2 dopamine agonist RU 24213-induced behavioral alterations in the mouse were determined by using multidimensional behavioral analyses based upon a capacitance system. Although dynorphin A(1-13) (3.0 or 12.5 micrograms) alone did not produce any significant effects on behaviors, the peptide (12.5 micrograms) caused an inhibitory effect on the RU 24213 (3.0 mg/kg)-induced increase in behavioral patterns such as linear locomotion and circling except rearing and grooming behaviors. The antagonistic effects of dynorphin A(1-313) (12.5 micrograms) were fully reversed by the opioid antagonist M(r) 2266 (10.0 mg/kg). However, dynorphin A(1-13) (3.0 or 12.5 micrograms) failed to affect behaviors elicited by SK&F 38393 (10.0 mg/kg). These results suggest that dynorphin A(1-13) plays an inhibitory role in behaviors induced by the D2 dopamine agonist but not by the D1 dopamine agonist, possibly through the mediation of kappa-opioid receptors.
通过基于电容系统的多维行为分析,确定了强啡肽A(1 - 13)对D1多巴胺激动剂SK&F 38393和D2多巴胺激动剂RU 24213诱导的小鼠行为改变的影响。尽管单独使用强啡肽A(1 - 13)(3.0或12.5微克)对行为没有产生任何显著影响,但该肽(12.5微克)对RU 24213(3.0毫克/千克)诱导的行为模式增加具有抑制作用,如直线运动和转圈,但不包括竖毛和梳理行为。强啡肽A(1 - 13)(12.5微克)的拮抗作用可被阿片类拮抗剂M(r) 2266(10.0毫克/千克)完全逆转。然而,强啡肽A(1 - 13)(3.0或12.5微克)未能影响SK&F 38393(10.0毫克/千克)引发的行为。这些结果表明,强啡肽A(1 - 13)可能通过κ-阿片受体的介导,对D2多巴胺激动剂诱导的行为起抑制作用,而对D1多巴胺激动剂诱导的行为无影响。