Mrunali D. Dhokne, Madhura P. Dixit, Mayur B. Kale, M. M. Aglawe, M. Umekar, B. Taksande
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引用次数: 0
摘要
n -甲基- d -天冬氨酸受体(NMDAR)拮抗剂是谷氨酸受体或一氧化氮合酶(NOS)抑制剂的一个亚类,可阻止神经元的可塑性。然而,神经可塑性在炎症和神经病变引起的疼痛中起着重要作用,这为使用NOS抑制剂和NMDAR拮抗剂治疗慢性疼痛提供了临床机会。神经调节剂agmatine具有NOS抑制和NMDAR拮抗活性,并控制脑和脊髓的一系列神经递质和信号通路。本文描述和探讨了胍丁胺对疼痛调节的影响,以及这些影响的潜在作用机制。我们特别提供证据来支持进一步的临床和临床前试验,研究胍丁氨酸作为神经性疼痛的新型治疗剂。
Agmatine as a Novel Treatment Option for Neuropathies: Experimental Evidences
N-methyl-D-aspartate receptor (NMDAR) antagonist, a subclass of glutamate receptors or nitric oxide synthase (NOS) inhibitors, prevents neuronal plasticity. However, neural plasticity plays a major role in the pain caused by inflammation and neuropathy, providing clinical opportunities for the use of NOS inhibitors and NMDAR antagonists in the treatment of chronic pain. The neuromodulator agmatine has both NOS inhibitory and NMDAR antagonistic activity, and it controls a range of neurotransmitters and signaling pathways in the brain and spinal cord. The effects of agmatine on pain modulation are described and explored in this article, along with a potential mechanism of action for these effects. We specifically offer evidence to support further clinical and pre-clinical trials looking into agmatine as a novel therapeutic agent for neuropathic pain.