Mechanism of the dynorphin-induced dualistic effect on free intracellular Ca2+ concentration in cultured rat spinal neurons

被引:12
|
作者
Hu, WH [1 ]
Zhang, CH
Yang, HF
Zheng, YF
Liu, N
Sun, XJ
Jen, J
Jen, MF
机构
[1] Third Mil Med Acad, Inst Surg Res, Chongqing 630042, Peoples R China
[2] Chinese Acad Med Sci, Inst Basic Med Sci, Dept Pharmacol, Beijing 100005, Peoples R China
[3] Sch Basic Med, Beijing 100005, Peoples R China
[4] Chinese Acad Med Sci, Inst Basic Med Sci, Dept Physiol, Beijing 100005, Peoples R China
基金
中国国家自然科学基金;
关键词
dynorphin; Ca2+; (neuron); spinal cord; cell culture; glutamate receptor; (rat); fura-2;
D O I
10.1016/S0014-2999(97)01492-1
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
In order to study the different mechanisms of dynorphin spinal analgesia and neurotoxicity at low and high doses, the effects of various concentrations of dynorphin A-(1-17) on the free intracellular Ca2+ concentration ([Ca2+](i)) in the cultured rat spinal neurons were studied using single cell microspectrofluorimetry. While dynorphin A-(1-17) 0.1-100 mu M had no significant effect on basal [Ca2+](i), dynorphin A-(1-17) 0.1 and 1 mu M significantly decreased the high KCl-evoked peak [Ca2+](i) by 94% and 83% respectively. Dynorphin A-(1-17) 10 and 100 mu M did not affect the peak [Ca2+](i) following K+ depolarization, but in all these neurons there was a sustained and irreversible rise in [Ca2+](i) following high-K+ challenge. Pretreatment with the specific kappa-opioid receptor antagonist nor-binaltorphimine 10 mu M, but not the competitive NMDA receptor antagonist, DL-2-amino-5-phosphonovalerate (APV) 10 mu M, significantly blocked the inhibitory effect of dynorphin A-(1-17) 0.1 mu M on peak [Ca2+](i). However, APV 10 mu M and nor-binaltorphimine 10 mu M significantly antagonized the sustained rise in [Ca2+](i) induced by a high concentration of dynorphin A-(1-17) 10 mu M. Furthermore, in the presence, and following the addition, of increasing concentrations of dynorphin A-(1-17) (0.1, 1, 10 and 100 mu M), the high concentrations of dynorphin A-(1-17) failed to produce a sustained rise in peak [Ca2+](i). These results suggested that dynorphin exerted a dualistic modulatory effect on [Ca2+](i) in cultured rat spinal neurons, inducing a sustained and irreversible intracellular Ca2+ overload via activation of both NMDA and kappa-opioid receptors at higher concentrations, but inhibiting depolarization-evoked Ca2+ influx via kappa-opioid but not NMDA receptors at lower concentrations. Serial addition of graded concentrations of dynorphin A-(1-17) prevented the effect of high concentrations of dynorphin A-(1-17) on [Ca2+](i). (C) 1998 Elsevier Science B.V.
引用
收藏
页码:325 / 332
页数:8
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