Werz M A, Macdonald R L
Neuropeptides. 1984 Dec;5(1-3):253-6. doi: 10.1016/0143-4179(84)90075-1.
Dynorphin A (DYN) (1 microM) decreased somatic calcium-dependent action potential (CAP) duration of a portion of dorsal root ganglion (DRG) neurons in a naloxone reversible manner. Responses to DYN differed from responses to Leu-enkephalin in that only DYN decreases of somatic CAP duration were associated with decreased action potential after hyperpolarization and persisted after intracellular injection of the potassium channel blocker cesium. While Leu-enkephalin at 10 microM did not affect somatic CAP duration of DRG neurons impaled with cesium-filled micropipettes, dynorphin A (1-8), dynorphin B, and beta-neoendorphin were effective at 1 microM. During single electrode voltage clamp, DYN decreased inward current in a portion of DRG neurons under conditions that predominately isolated calcium current. Leak current was unaffected by dynorphin A. Therefore, we suggest that DYN decreases voltage-dependent calcium conductance. The action on calcium conductance appears specific for opioids with affinity for kappa-receptors.
强啡肽A(DYN)(1微摩尔)以纳洛酮可逆的方式缩短了一部分背根神经节(DRG)神经元的体细胞钙依赖性动作电位(CAP)持续时间。对DYN的反应与对亮氨酸脑啡肽的反应不同,因为只有DYN缩短体细胞CAP持续时间与动作电位超极化后降低相关,并且在细胞内注射钾通道阻滞剂铯后仍然存在。虽然10微摩尔的亮氨酸脑啡肽不影响用充满铯的微电极刺入的DRG神经元的体细胞CAP持续时间,但强啡肽A(1-8)、强啡肽B和β-新内啡肽在1微摩尔时有效。在单电极电压钳制期间,在主要分离钙电流的条件下,DYN降低了一部分DRG神经元的内向电流。泄漏电流不受强啡肽A的影响。因此,我们认为DYN降低电压依赖性钙电导。对钙电导的作用似乎对与κ受体具有亲和力的阿片类药物具有特异性。