Gaddis R R, Dixon W R
Pharmacology. 1985;30(4):205-14. doi: 10.1159/000138070.
The pre- and postsynaptic effects of ethylketocyclazocine (EKC), a putative kappa opiate receptor agonist, on sympathetic adrenergic neurotransmission were investigated using the isolated perfused cat spleen. Perfusion of spleens with EKC (10(-7) and 10(-6)M) produced a modest dose-dependent inhibition of nerve-stimulation-mediated overflow of norepinephrine (NE) and total 3H. In contrast, EKC (10(-4)M) produced an increase in the release of NE, and total 3H overflow. Perfusion with EKC (10(-5) and 10(-4)M) resulted in a dose-dependent inhibition of the postsynaptic response to stimulation-mediated release of NE. Likewise, EKC inhibited splenic contraction due to exogenously administered NE which was not antagonized by naloxone. These results suggest that EKC exerts a direct effect on peripheral adrenergic neurotransmission not mediated via classical kappa opiate receptors.
使用离体灌注的猫脾脏,研究了假定的κ阿片受体激动剂乙基酮环唑辛(EKC)对交感肾上腺素能神经传递的突触前和突触后效应。用EKC(10^(-7)和10^(-6)M)灌注脾脏,对神经刺激介导的去甲肾上腺素(NE)和总3H溢出产生适度的剂量依赖性抑制。相反,EKC(10^(-4)M)使NE释放和总3H溢出增加。用EKC(10^(-5)和10^(-4)M)灌注导致对刺激介导的NE释放的突触后反应产生剂量依赖性抑制。同样,EKC抑制了外源性给予NE引起的脾脏收缩,而纳洛酮不能拮抗这种作用。这些结果表明,EKC对周围肾上腺素能神经传递产生直接作用,并非通过经典的κ阿片受体介导。