Similar and different effects of capsaicin and resiniferatoxin on substance P release and transient receptor potential vanilloid type 1 expression of cultured rat dorsal root ganglion neurons.

X Yang, H Gong, Z Liu, H Liu, H Wang, Zhenzhong Li
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引用次数: 13

Abstract

The purpose of this study was to investigate the effects of capsaicin (CAP) and resiniferatoxin (RTX) on substance P (SP) release and transient receptor potential vanilloid type 1 (TRPV1) expression of cultured rat dorsal root ganglion (DRG) neurons. Dissociated DRG cells of embryonic 15-day-old Wistar rat were cultured for 3 days and then exposed to CAP (1 micromol/L, 10 micromol/L) or RTX (10 nmol/L, 100 nmol/L) for 10 min. At 3 days of culture growth, SP release increased significantly after 10 min of stimulation with CAP or RTX as compared with controls. Six days after acute exposure to CAP or RTX, SP release and SP expression of cultured rat DRG neurons decreased significantly in both CAP- and RTX-treated cultures as compared with controls. Preprotachykinin (PPT) mRNA, TRPV1 mRNA and TRPV1 protein expression decreased in CAP-treated cultures and RTX cultures treated with the higher concentration, whereas RTX cultures treated with the lower concentration were not affected. The results indicate that CAP and high concentrations of RTX are more neurotoxic to cultured rat DRG neurons while the inability of the neurons to express SP or TRPV1 after acute exposure to the lower concentration of RTX could be partially reversed after a period of incubation. The efficacy and therapeutic potential of the reversible action of RTX are more applicable as strategies for pain or neurogenic inflammation therapy.

辣椒素和树脂素毒素对培养大鼠背根神经节神经元P物质释放和瞬时受体电位香草样蛋白1型表达的异同影响
本研究旨在探讨辣椒素(CAP)和树脂干扰素(RTX)对培养大鼠背根神经节(DRG)神经元P物质(SP)释放和瞬时受体电位香草样蛋白1 (TRPV1)表达的影响。将15日龄Wistar大鼠胚胎DRG细胞分离后培养3 d,然后将其暴露于CAP(1微mol/L、10微mol/L)或RTX (10 nmol/L、100 nmol/L)中10 min。在培养生长3 d时,与对照组相比,CAP或RTX刺激10 min后SP释放显著增加。急性暴露于CAP或RTX 6天后,与对照组相比,CAP和RTX处理的大鼠DRG神经元的SP释放和SP表达均显著降低。在cap处理和RTX处理中,PPT mRNA、TRPV1 mRNA和TRPV1蛋白的表达均降低,而RTX处理对PPT mRNA、TRPV1 mRNA和TRPV1蛋白表达无影响。结果表明,CAP和高浓度RTX对培养的大鼠DRG神经元具有更大的神经毒性,而急性暴露于较低浓度RTX后神经元不能表达SP或TRPV1的现象在孵育一段时间后可以部分逆转。RTX的可逆作用的疗效和治疗潜力更适用于疼痛或神经源性炎症的治疗策略。
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