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基于肠道菌群探讨热量限制防治肥胖相关代谢性疾病的研究进展 被引量:2

Research progress of caloric restriction in the prevention and treatment of obesity related metabolic diseases based on gut microbiota
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摘要 肥胖及其相关代谢性疾病已成为全球范围内严重影响人类健康的疾病。研究发现,菌群紊乱引起条件致病菌和有害细菌代谢产物增多,参与肥胖相关代谢性疾病的发生发展。饮食是影响肠道菌群的关键因素之一。已有大量证据表明,作为饮食干预方式之一,热量限制可明显改善肥胖、糖尿病、非酒精性脂肪肝等代谢性疾病的症状,而肠道菌群可能是其作用靶点之一。本文从肥胖、糖尿病和非酒精性脂肪肝病的肠道菌群改变、热量限制对3种代谢性疾病的治疗效果以及肠道菌群在其中的介导作用3方面进行综述。 Obesity related metabolic diseases seriously affect human health all over the world.It's found that the disorder of gut microbiota leads to the increase of conditional pathogenic bacteria and harmful bacterial metabolites,which is involved in the occurrence and development of obesity related metabolic diseases.Diet is one of the important factors affecting gut microbiota.Caloric restriction as one of dietary intervention,a lot of evidence have proven that it can significantly improve the symptoms of metabolic diseases such as obesity,diabetes and nonalcoholic fatty liver disease.Gut microbiota may be one of its targets.Therefore,this paper reviews from such following three aspects as the changes of gut microbiota in obesity,diabetes and nonalcoholic fatty liver disease,the therapeutic effect of caloric restriction on these three metabolic diseases and the mediating role of gut microbiota in the process.
作者 叶佳美 钟冬灵 李涓 赵小华 庞日朝 张安仁 Ye Jiamei;Zhong Dongling;Li Juan;Zhao Xiaohua;Pang Rizhao;Zhang Anren(School of Health and Rehabilitation,Chengdu University of Traditional Chinese Medicine;Department of Rehabilitation Medicine,The General Hospital of Western Theater Command PLA)
出处 《重庆医科大学学报》 CAS CSCD 北大核心 2022年第6期676-682,共7页 Journal of Chongqing Medical University
基金 国家自然科学基金面上资助项目(编号:81973927)
关键词 热量限制 肠道菌群 肥胖 糖尿病 非酒精性脂肪肝 代谢性疾病 caloric restriction gut microbiota obesity diabetes nonalcoholic fatty liver disease metabolic disease
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  • 1Dutnall R N, Pillus L. Deciphering NAD-dependent deacetylases [J]. Cell, 2001, 105(2) :161-164.
  • 2Rusche L N, Kirchmaier A L, Rine J. The establishment, inheritance,and function of silenced chromatin in Saccharomyces cerevisiae[J]. Annu Rev Biochem, 2003, 72:481-516.
  • 3Dryden S C, Nahhas F A, Nowak J E, et al. Role for human Sirt2 NAD-dependent deacetylase activity in control of mitotic exit in the cellcycle[J]. MolCeIlBiol, 2003, 23(9) :3173-185.
  • 4Rodgers J T, Lerin C, Haas W, et al. Nutrient control of glucose homeostasis through a complex of PGC-lalpha and Sirtl [ J ]. Nature, 2005, 434(7029) : 113-118.
  • 5Langley E, Pearson M, Faretta M, et al. Human Sir2 deacetylates p53 and antagonizes PML/p53- induced cellular seneseenee[Jl. EMBO J, 2002, 21(10):2383-2396.
  • 6Haigis M C, Guarente L P. Mammalian sirtuins - emerging roles in physiology, aging, and calorie restriction [ J]. Genes Dev,2006, 20(21 ) :2913-2921.
  • 7North B J, Verdin E. Sirtuins: Sir2-related NAD-dependent protein deacetylases [ J ]. Genome Biol, 2004, 5 ( 5 ) :224.
  • 8Bellizzi D, Covello G, Di Cianni F, et al. Identification of GATA2 and AP-1 Activator elements within the enhancer VNTR occurring in intron 5 of the human Sirt3 gene [ J]. Mol Cells, 2009, 28(2) :87-92.
  • 9Shi T, Wang F, Stieren E, et al. Sirt3, a mitoehondrial sirtuin deacetylase, regulates mitochondrial function and thermogenesis in brown adipocytes [J]. J Biol Chem, 2005, 280(14) : 13560- 13567.
  • 10Chandler P C, Viana J B, Oswald K D, et al. Feeding response to melanoeortin agonist predicts preference for and obesity from a high-fat diet [ J ]. Physiol Behav, 2005, 85 ( 2 ) : 221-230.

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