单位:[1]Molecular Laboratory for Gene Therapy and Tooth Regeneration, Beijing Key Laboratory of Tooth Regeneration and FunctionReconstruction, Capital Medical University School of Stomatology, Beijing 100050, China[2]Department of Stomatology, Beijing Bo’ai Hospital, China Rehabilitation Research Center, School of Rehabilitation, Capital MedicalUniversity, Beijing 100068, China[3]Laboratory of Molecular Signaling and Stem Cells Therapy, Beijing Key Laboratory of Tooth Regeneration and Function Reconstruction,School of Stomatology, Capital Medical University, Beijing 100050, China[4]Department of Biochemistry and Molecular Biology, Capital Medical University School of Basic Medical Sciences, Beijing 100069, China[5]Liver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China临床科室国家中心肝病分中心首都医科大学附属北京友谊医院
Senescence-related decline in liver function is a common complication in the elderly that can lead to impaired health in older individuals. Dietary nitrate supplements have physiological and therapeutic effects on organ function by nitrate (NO3 (-))-nitrite (NO2 (-))-nitric oxide (NO) pathway. However, the role of dietary nitrate on the senescence-related decline in liver function is unclear. The findings of the present study showed that nitrate levels in the serum and liver decreased, whereas the levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST) in serum increased in ageing mice. Consistently, cell senescence, decreased glycogen levels and increased lipid deposition were found in the liver of aged mice, both glucokinase (GCK) and phosphoenolpyruvate carboxykinase (PCK) were down-regulated (n=10). Daily nitrate intake (0.5 mmol L-1) restored nitrate levels, decreased ALT and AST levels, and prevented cell senescence and structural and glucose and lipid metabolism degeneration in liver tissue both in D-galactose (D-gal)-induced ageing mice (n=10) and in natural aged mice (n=10). In conclusion, the present study demonstrated that the reduction of nitrate levels was correlated with liver degeneration in ageing individuals and that dietary supplement of nitrate could restore the nitrate levels in serum and the liver and prevent ageing-related liver degeneration.
基金:
National Natural Science Foundation of ChinaNational Natural Science Foundation of China (NSFC) [91649124]; Beijing Municipality Government grants (Beijing Scholar Program) [Z121100-005212004, PXM2013_014226_000055, PXM2013_014226_000021, PXM 2013_014226_07_000080, TJSHG201310025005]; National Natural Science FoundationNational Natural Science Foundation of China (NSFC) [PXM2016_014226_000034, PXM2016_014226_000006, PXM2015_014226_000116, PXM2015_014226_000055, PXM2015_014226_000052, PXM2014_014226_000048, PXM2014_014226_000013, PXM2014_014226_000053]
第一作者单位:[1]Molecular Laboratory for Gene Therapy and Tooth Regeneration, Beijing Key Laboratory of Tooth Regeneration and FunctionReconstruction, Capital Medical University School of Stomatology, Beijing 100050, China[2]Department of Stomatology, Beijing Bo’ai Hospital, China Rehabilitation Research Center, School of Rehabilitation, Capital MedicalUniversity, Beijing 100068, China
共同第一作者:
通讯作者:
通讯机构:[1]Molecular Laboratory for Gene Therapy and Tooth Regeneration, Beijing Key Laboratory of Tooth Regeneration and FunctionReconstruction, Capital Medical University School of Stomatology, Beijing 100050, China[4]Department of Biochemistry and Molecular Biology, Capital Medical University School of Basic Medical Sciences, Beijing 100069, China
推荐引用方式(GB/T 7714):
Haifeng Wang,Lei Hu,Le Li,et al.Inorganic nitrate alleviates the senescence-related decline in liver function[J].SCIENCE CHINA-LIFE SCIENCES.2018,61(1):24-34.doi:10.1007/s11427-017-9207-x.
APA:
Haifeng Wang,Lei Hu,Le Li,Xiaoshan Wu,Zhipeng Fan...&Songlin Wang.(2018).Inorganic nitrate alleviates the senescence-related decline in liver function.SCIENCE CHINA-LIFE SCIENCES,61,(1)
MLA:
Haifeng Wang,et al."Inorganic nitrate alleviates the senescence-related decline in liver function".SCIENCE CHINA-LIFE SCIENCES 61..1(2018):24-34