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Metabolomic analysis reveals a protective effect of Fu-Fang-Jin-Qian-Chao herbal granules on oxalate-induced kidney injury.
Chen, Wei; Liu, Wen-Rui; Hou, Jie-Bin; Ding, Jia-Rong; Peng, Zhong-Jiang; Gao, Song-Yan; Dong, Xin; Ma, Jun-Hua; Lin, Qi-Shan; Lu, Jian-Rao; Guo, Zhi-Yong.
Afiliação
  • Chen W; Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
  • Liu WR; Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
  • Hou JB; Department of Nephrology, Seventh People's Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai 200137, China.
  • Ding JR; Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
  • Peng ZJ; Department of Geriatric Nephrology, Chinese PLA General Hospital, Beijing 100853, China.
  • Gao SY; Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
  • Dong X; Changhai Hospital, Second Military Medical University, Shanghai 200433, China.
  • Ma JH; School of Pharmacy, Second Military Medical University, Shanghai 200433, China.
  • Lin QS; School of Pharmacy, Second Military Medical University, Shanghai 200433, China.
  • Lu JR; Guangxi Wantong Pharmaceutical Co., Ltd, 16 Dong Erli, South Zhongyao Road, Nanning, Guangxi 530003, China.
  • Guo ZY; Proteomics/Mass Spec Facility, Center for Functional Genomics, University at Albany, Rensselaer, NY 12144, U.S.A.
Biosci Rep ; 39(2)2019 02 28.
Article em En | MEDLINE | ID: mdl-30737304
Nephrolithiasis is one of the world's major public health burdens with a high incidence and a risk of persistent renal dysfunction. Fu-Fang-Jin-Qian-Chao granules (FFJQC), a traditional Chinese herb formula, is commonly used in treatment of nephrolithiasis. However, the therapeutic mechanism of FFJQC on kidney stone has still been a mystery. The objective of the present study is to explore the therapeutic mechanism of FFJQC on kidney injury and identify unique metabolomics patterns using a mouse model of kidney stone induced by a calcium oxalate (CaOx) deposition. Von Kossa staining and immuno-histopathological staining of osteopontin (OPN), cluster of differentiation 44 (CD44) and calbindin-D28k were conducted on renal sections. Biochemical analysis was performed on serum, urine, and kidney tissues. A metabolomics approach based on ultra-HPLC coupled with quadrupole-TOF-MS (UHPLC-Q-TOF/MS) was used for serum metabolic profiling. The immunohistopathological and biochemical analysis showed the therapeutic benefits of FFJQC. The expression levels of OPN and CD44 were decreased while calbindin-D28k increased after the CaOx injured mice were treated with FFJQC. In addition, total of 81 serum metabolites were identified to be associated with protective effects of FFJQC on CaOx crystal injured mice. Most of these metabolites were involved in purine, amino acid, membrane lipid and energy metabolism. Potential metabolite biomarkers were found for CaOx crystal-induced renal damage. Potential metabolite biomarkers of CaOx crystal-induced renal damage were found. FFJQC shows therapeutic benefits on CaOx crystal injured mice via regulation of multiple metabolic pathways including amino acids, purine, pyrimidine, glycerolipid, arachidonic acid (AA), sphingolipid, glycerophospholipid, and fatty acid.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Medicamentos de Ervas Chinesas / Cálculos Renais / Substâncias Protetoras / Metaboloma / Rim Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Medicamentos de Ervas Chinesas / Cálculos Renais / Substâncias Protetoras / Metaboloma / Rim Tipo de estudo: Etiology_studies Limite: Animals Idioma: En Ano de publicação: 2019 Tipo de documento: Article