Kumrungsee Thanutchaporn, Yanaka Noriyuki, Suda Takashi, Kato Norihisa
Graduate School of Integrated Sciences for Life, Hiroshima University, Higashi-Hiroshima, 739-8528, Japan.
State Key Laboratory of Cellular Stress Biology, School of Medicine & School of Life Science, Xiamen University, Xiamen, Fujian, China.
Eur J Nutr. 2022 Mar;61(2):605-613. doi: 10.1007/s00394-021-02665-2. Epub 2021 Aug 26.
Although overt vitamin B6 deficiency is rare, marginal vitamin B6 deficiency is frequent and occurs in a consistent proportion of the population. The marginal vitamin B6 deficiency appears to relate to an increased risk of inflammation-related diseases, such as cardiovascular diseases and cancers. Of all the cardiovascular diseases, heart failure is a complex clinical syndrome associated with a high mortality rate. So far, information regarding the cardioprotective mechanisms of vitamin B6 has been limited. Meanwhile, recent studies have revealed that vitamin B6 treatment increases cardiac levels of imidazole dipeptides (e.g., carnosine, anserine, and homocarnosine), histamine, and γ-aminobutyric acid (GABA) and suppresses P2X7 receptor-mediated NLRP3 inflammasome. These modulations may imply potential cardioprotective mechanisms of vitamin B6. These modulations may also be involved in the underlying mechanisms through which vitamin B6 suppresses oxidative stress and inflammation. This review provides an up-to-date evaluation of our current understanding of the cardioprotective mechanisms of vitamin B6.
尽管明显的维生素B6缺乏症很少见,但边缘性维生素B6缺乏症却很常见,且在一定比例的人群中存在。边缘性维生素B6缺乏症似乎与炎症相关疾病(如心血管疾病和癌症)的风险增加有关。在所有心血管疾病中,心力衰竭是一种复杂的临床综合征,死亡率很高。到目前为止,关于维生素B6心脏保护机制的信息有限。同时,最近的研究表明,维生素B6治疗可增加心脏中咪唑二肽(如肌肽、鹅肌肽和高肌肽)、组胺和γ-氨基丁酸(GABA)的水平,并抑制P2X7受体介导的NLRP3炎性小体。这些调节可能暗示维生素B6潜在的心脏保护机制。这些调节也可能参与了维生素B6抑制氧化应激和炎症的潜在机制。本综述对我们目前对维生素B6心脏保护机制的理解进行了最新评估。