Young Shim Eun, Jung Kim Hee, Kim Myung-Jun, Rhie Duck-Joo, Jo Yang-Hyeok, Kim Myung-Suk, June Hahn Sang, Lee Mun-Yong, Yoon Shin Hee
Department of Physiology, College of Medicine, The Catholic University of Korea, 505 Banpo-dong, Socho-gu, Seoul 137-701, South Korea.
Brain Res. 2006 Sep 21;1111(1):61-71. doi: 10.1016/j.brainres.2006.06.081. Epub 2006 Aug 1.
Neuronal excitability is inhibited by somatostatin, which might play important roles in seizure and neuroprotection. The possibility of whether the effect of somatostatin on neurotransmission is susceptible to desensitization was investigated. We tested the effects of prolonged exposure to somatostatin on 0.1 mM extracellular Mg(2+) concentration (Mg(2+))-induced intracellular free Ca(2+) concentration (Ca(2+)) spikes in cultured rat hippocampal neurons using fura-2-based microfluorimetry. Reducing Mg(2+) to 0.1 mM elicited repetitive Ca(2+) spikes. These Ca(2+) spikes were inhibited by exposure to somatostatin-14. The inhibitory effects of somatostatin were blocked by pretreatment with pertussis toxin (PTX, 100 ng/ml) for 18-24 h. Prolonged exposure to somatostatin induced a desensitization of the somatostatin-induced inhibition of Ca(2+) spikes in a concentration-dependent manner. The somatostatin-induced desensitization was retarded by the nonspecific protein kinase C (PKC) inhibitor staurosporin (100 nM) or chronic treatment with phorbol dibutyrate (1 microM) for 24 h, but not by the protein kinase A inhibitor KT5720. The desensitization was significantly retarded by the novel PKCepsilon translocation inhibitor peptide (1 microM). In addition, suramin (3 microM), an inhibitor of G-protein-coupled receptor kinase 2 (GRK2), caused a reduction in the desensitization. After tetrodotoxin (TTX, 1 microM) completely blocked the low Mg(2+)-induced Ca(2+) spikes, glutamate-induced Ca(2+) transients were slightly inhibited by somatostatin and the inhibition was desensitized by prolonged exposure to somatostatin. These results indicate that the prolonged activation of somatostatin receptors induces the desensitization of somatostatin-induced inhibition on low Mg(2+)-induced Ca(2+) spikes through the activation of GRK2 and partly a novel PKCepsilon in cultured rat hippocampal neurons.
生长抑素可抑制神经元兴奋性,其可能在癫痫发作和神经保护中发挥重要作用。本研究探讨了生长抑素对神经传递的作用是否易于脱敏。我们使用基于fura-2的显微荧光测定法,检测了长时间暴露于生长抑素对0.1 mM细胞外镁离子浓度(Mg(2+))诱导的培养大鼠海马神经元细胞内游离钙离子浓度(Ca(2+))尖峰的影响。将Mg(2+)降至0.1 mM会引发重复性的Ca(2+)尖峰。这些Ca(2+)尖峰受到生长抑素-14暴露的抑制。生长抑素的抑制作用可被百日咳毒素(PTX,100 ng/ml)预处理18 - 24小时所阻断。长时间暴露于生长抑素会以浓度依赖的方式诱导生长抑素对Ca(2+)尖峰抑制作用的脱敏。生长抑素诱导的脱敏作用可被非特异性蛋白激酶C(PKC)抑制剂星形孢菌素(100 nM)或用佛波酯(1 microM)慢性处理24小时所延迟,但蛋白激酶A抑制剂KT5720则无此作用。新型PKCepsilon易位抑制剂肽(1 microM)可显著延迟脱敏作用。此外,G蛋白偶联受体激酶2(GRK2)抑制剂苏拉明(3 microM)可减少脱敏作用。在河豚毒素(TTX,1 microM)完全阻断低Mg(2+)诱导的Ca(2+)尖峰后,谷氨酸诱导的Ca(2+)瞬变会受到生长抑素的轻微抑制,且长时间暴露于生长抑素会使这种抑制作用脱敏。这些结果表明,生长抑素受体的长时间激活通过GRK2和部分新型PKCepsilon的激活,诱导生长抑素对低Mg(2+)诱导的Ca(2+)尖峰抑制作用的脱敏,该过程发生在培养的大鼠海马神经元中。