1 Department of Cellular and Molecular Medicine, Cleveland Clinic Lerner Research Institute , Cleveland, Ohio.
2 Division of Endocrinology, Diabetes and Metabolism, Beth Israel Deaconess Medical Center and Harvard Medical School , Boston, Massachusetts.
Antioxid Redox Signal. 2018 Jun 1;28(16):1483-1502. doi: 10.1089/ars.2017.7434.
Hydrogen sulfide (HS) at the right concentration is associated with numerous health benefits in experimental organisms, ranging from protection from ischemia/reperfusion injury to life span extension. Given the considerable translation potential, two major strategies have emerged: supplementation of exogenous HS and modulation of endogenous HS metabolism. Recent Advances: Recently, it was reported that hepatic HS production capacity is increased in two of the best-characterized mammalian models of life span extension, dietary restriction, and hypopituitary dwarfism, leading to new insights into dietary and hormonal regulation of endogenous HS production together with broader changes in sulfur amino acid (SAA) metabolism with implications for DNA methylation and redox status.
Here, we discuss the role of dietary SAAs and growth hormone (GH)/thyroid hormone (TH) signaling in regulation of endogenous HS production largely via repression of HS generating enzymes cystathionine γ-lyase (CGL) and cystathionine β-synthase (CBS) on the level of gene transcription, as well as reciprocal regulation of GH and TH signaling by HS itself. We also discuss plasticity of CGL and CBS gene expression in response to environmental stimuli and the potential of the microbiome to impact overall HS levels.
The relative contribution of increased HS to health span or lifespan benefits in models of extended longevity remains to be determined, as does the mechanism by which such benefits occur. Nonetheless, our ability to control HS levels using exogenous HS donors or by modifying the endogenous HS production/consumption equilibrium has the potential to improve health and increase "shelf-life" across evolutionary boundaries, including our own. Antioxid. Redox Signal. 28, 1483-1502.
在实验生物中,适量的硫化氢(HS)与许多健康益处相关,范围从对缺血/再灌注损伤的保护到寿命延长。鉴于其巨大的转化潜力,出现了两种主要策略:外源性 HS 的补充和内源性 HS 代谢的调节。最新进展:最近,据报道,两种最典型的延长寿命的哺乳动物模型(饮食限制和垂体功能减退性侏儒症)中,肝脏 HS 产生能力增加,这为饮食和激素对内源性 HS 产生的调节以及更广泛的硫氨基酸(SAA)代谢变化提供了新的见解,这些变化对 DNA 甲基化和氧化还原状态有影响。
在这里,我们讨论了饮食 SAA 和生长激素(GH)/甲状腺激素(TH)信号在调节内源性 HS 产生中的作用,主要是通过抑制 HS 生成酶胱硫醚γ-裂解酶(CGL)和胱硫醚β-合酶(CBS)在基因转录水平上,以及 HS 本身对 GH 和 TH 信号的相互调节。我们还讨论了 CGL 和 CBS 基因表达对环境刺激的可塑性,以及微生物组对整体 HS 水平的潜在影响。
在延长寿命的模型中,增加的 HS 对健康跨度或寿命益处的相对贡献仍有待确定,以及这种益处发生的机制。尽管如此,我们使用外源性 HS 供体或通过调节内源性 HS 产生/消耗平衡来控制 HS 水平的能力有可能改善健康并延长跨越进化界限的“保质期”,包括我们自己的。抗氧化剂。氧化还原信号。28,1483-1502。