[The role of CaSR expression in diabetic cirrhosis injury and fibrosis in rats].


Journal

Zhongguo ying yong sheng li xue za zhi = Zhongguo yingyong shenglixue zazhi = Chinese journal of applied physiology
ISSN: 1000-6834
Titre abrégé: Zhongguo Ying Yong Sheng Li Xue Za Zhi
Pays: China
ID NLM: 9426407

Informations de publication

Date de publication:
28 Jan 2020
Historique:
entrez: 2 6 2020
pubmed: 2 6 2020
medline: 1 7 2020
Statut: ppublish

Résumé

To observe the role of calcium sensitive receptor (CaSR) in the pathogenesis of diabetic liver injury. Forty Wistar rats were randomly divided into normal control group (control, n=10) and diabetes group (T1D, STZ 60 mg/kg intraperitoneal injection, n=30), and the samples were collected at the 2nd, 4th and 8th week. Rats hepatic stellate cells (HSC) were randomly divided into normal control group (Control, 10% FBS-DMEM culture, n=5), high glucose group (HG, 10% FBS-DMEM+40 mmol/L glucose, treated for 48 h, n=5) and CaSR inhibitor group (HG+Calhex 231, 10% FBS-DMEM+40 mmol/L glucose+2.5 μmol/L Calhex Compared with the control group, diabetic rats lost weight, while blood glucose, AST and ALT increased significantly, and the expression of CaSR, collagen 1(CO 1), collagen 3 (CO 3), matrix metalloproteinase(MMP)-1, -2 and -9 increased significantly. The results of the cell model were basically the same as those in vivo. Compared with the control group, the expression of α-smooth muscle actin (α-SMA) was increased, indicating that HSC differentiated into myofibroblasts in HG group. The expression of the main components of ECM (CO 1 and CO 3), and the key enzyme of ECM degradation (MMP9) were also increased, while CaSR inhibitor, Calhex The up-regulation of CaSR expression is involved in the occurrence of diabetic liver injury and fibrosis.

Identifiants

pubmed: 32476365
doi: 10.12047/j.cjap.5813.2020.001
doi:

Substances chimiques

Receptors, Calcium-Sensing 0
Matrix Metalloproteinases EC 3.4.24.-

Types de publication

Journal Article

Langues

chi

Sous-ensembles de citation

IM

Pagination

1-5

Auteurs

Yi-Ying Shao (YY)

Department of Pathophysiology, Harbin Medical University, Harbin 150086, China.

Yu-Qi Fan (YQ)

Department of Pathophysiology, Harbin Medical University, Harbin 150086, China.

Si-Wei Li (SW)

Department of Pathophysiology, Harbin Medical University, Harbin 150086, China.

Bing-Bing Zhao (BB)

Department of Pathophysiology, Harbin Medical University, Harbin 150086, China.

Xiao-Ting Shao (XT)

Department of Pathophysiology, Harbin Medical University, Harbin 150086, China.

Jing Hu (J)

Department of Pathophysiology, Harbin Medical University, Harbin 150086, China.

Chang-Qing Xu (CQ)

Department of Pathophysiology, Harbin Medical University, Harbin 150086, China.

Can Wei (C)

Department of Pathophysiology, Harbin Medical University, Harbin 150086, China.

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Classifications MeSH