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大剂量生物素的神经保护潜力。

Neuroprotective potential of high-dose biotin.

机构信息

Catalytic Longevity, 811 B Nahant Ct., San Diego, CA 92109, USA.

Mid America Heart Institute, St. Luke's Hospital, Kansas City, MO, USA.

出版信息

Med Hypotheses. 2017 Nov;109:145-149. doi: 10.1016/j.mehy.2017.10.012. Epub 2017 Oct 16.

Abstract

A recent controlled trial has established that high-dose biotin supplementation - 100 mg, three times daily - has a stabilizing effect on progression of multiple sclerosis (MS). Although this effect has been attributed to an optimization of biotin's essential cofactor role in the brain, a case can be made that direct stimulation of soluble guanylate cyclase (sGC) by pharmacological concentrations of biotin plays a key role in this regard. The utility of high-dose biotin in MS might reflect an anti-inflammatory effect of cGMP on the cerebral microvasculature, as well on oligodendrocyte differentiation and on Schwann cell production of neurotrophic factors thought to have potential for managing MS. But biotin's ability to boost cGMP synthesis in the brain may have broader neuroprotective potential. In many types of neurons and neural cells, cGMP exerts neurotrophic-mimetic effects - entailing activation of the PI3K-Akt and Ras-ERK pathways - that promote neuron survival and plasticity. Hippocampal long term potentiation requires nitric oxide synthesis, which in turn promotes an activating phosphorylation of CREB via a pathway involving cGMP and protein kinase G (PKG). In Alzheimer's disease (AD), amyloid beta suppresses this mechanism by inhibiting sGC activity; agents which exert a countervailing effect by boosting cGMP levels tend to restore effective long-term potentiation in rodent models of AD. Moreover, NO/cGMP suppresses amyloid beta production within the brain by inhibiting expression of amyloid precursor protein and BACE1. In conjunction with cGMP's ability to oppose neuron apoptosis, these effects suggest that high-dose biotin might have potential for the prevention and management of AD. cGMP also promotes neurogenesis, and may lessen stroke risk by impeding atherogenesis and hypertrophic remodeling in the cerebral vasculature. The neuroprotective potential of high-dose biotin likely could be boosted by concurrent administration of brain-permeable phosphodiesterase-5 inhibitors.

摘要

最近的一项对照试验证实,高剂量生物素补充剂(每日三次,每次 100mg)对多发性硬化症(MS)的进展具有稳定作用。虽然这种作用归因于生物素在大脑中必需辅酶作用的优化,但可以认为生物素的药理学浓度对可溶性鸟苷酸环化酶(sGC)的直接刺激在这方面起着关键作用。高剂量生物素在 MS 中的应用可能反映了 cGMP 对大脑微血管的抗炎作用,以及对少突胶质细胞分化和施万细胞产生神经营养因子的作用,这些因子可能具有管理 MS 的潜力。但是,生物素在大脑中增加 cGMP 合成的能力可能具有更广泛的神经保护潜力。在许多类型的神经元和神经细胞中,cGMP 发挥神经营养模拟作用-需要激活 PI3K-Akt 和 Ras-ERK 途径-促进神经元存活和可塑性。海马长时程增强需要一氧化氮合成,这反过来又通过涉及 cGMP 和蛋白激酶 G(PKG)的途径促进 CREB 的激活磷酸化。在阿尔茨海默病(AD)中,淀粉样蛋白β通过抑制 sGC 活性来抑制这种机制;通过提高 cGMP 水平来发挥拮抗作用的药物往往会在 AD 的啮齿动物模型中恢复有效的长时程增强。此外,NO/cGMP 通过抑制淀粉样前体蛋白和 BACE1 的表达来抑制大脑中淀粉样蛋白β的产生。与 cGMP 反对神经元凋亡的能力相结合,这些作用表明高剂量生物素可能具有预防和管理 AD 的潜力。cGMP 还促进神经发生,并通过阻碍脑血管的动脉粥样形成和肥厚重塑来降低中风风险。高剂量生物素的神经保护潜力可能通过同时给予脑渗透型磷酸二酯酶-5 抑制剂来增强。

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