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GW24-e3625 Effects of apelin on the phosphodiesterase 1 expression and oxidative stress levels in mouse kidney fibroblast cells
  1. JiuChang Zhong1,
  2. Bei Song1,
  3. Xiaoxiao Zhang1,
  4. Zhenzhou Zhang1,
  5. Gavin Y Oudit2,
  6. Xu Yingle1,
  7. Pingjin Gao1,
  8. Jiguang Wang1
  1. 1State Key Laboratory of Medical Genomics, Ruijin Hospital Affiliated to Shanghai Jiao Tong University School of Medicine, Shanghai Institute of Hypert
  2. 2Department of Medicine, University of Alberta; Mazankowski Alberta Heart Institute

Abstract

Objectives Apelin is a recently-discovered cardiovascular bioactive polypeptide with multiple biological effects, which is the endogenous ligand of the orphan G protein-coupled receptor-APJ receptor and may cause vasodilation and lower blood pressure levels. This study focused on the effects of Apelin on the phosphodiesterase 1 (PDE1) expression and oxidative stress levels in mouse kidney fibroblast cells.

Methods The mouse kidney fibroblast cells were primary cultured using the routine method. The angiotensin II (Ang II; 100 nmol/L) was used to stimulate the cells for 1 h in the presence and absence of Aplein (100 nmol/L), PDE1 inhibitor vinpocetine (10 μmol/L) and extracellular regulated protein kinase (ERK) inhibitor PD98059 (10 mmol/L). The specific fluorescent probe-dihydropyridinum (DHE) staining and colorimetric method were used for the determination of superoxide generation and malondialdehyde (MDA) content in cells, respectively.

Results In the cultured mouse kidney fibroblast cells, exposure to Ang II (100 nmol/L) obviously promoted protein expressions of PDE1A and PDE1B (n = 5-6; P < 0.01, respectively), without having a differential effect on the expression of PDE1C. These changes were associated with marked increases in phosphorylated expression of ERK1/2, superoxide generation and MDA levels (n = 5-6; P < 0.01, respectively). In addition, treatment with Apelin (100 nmol/L) and PDE1 inhibition with vinpocetine (10 μmol/L) significantly prevented expressions of PDE1A and PDE1B mediated by Ang II in cells (n = 5; P < 0.05, respectively). More importantly, intervention with Apelin (100 nmol/L) and vinpocetine (10 μmol/L) strikingly reduced the cellular oxidative stress in response to Ang II, as evidenced by decreases in MDA levels and superoxide production, linked with a marked downregulation in phosphorylated ERK1/2 levels (n = 5-6; P < 0.05 or P < 0.01, respectively).

Conclusions Treatment withApelin significantly prevents the oxidative stress formation in cultured mouse kidney fibroblast cells in response to Ang II through the modulation of PDE1-ERK1/2 signalling pathway, suggesting the potential anti-oxidative stress effect of Apelin. The enhanced activities and/or expression of Apelin may have potential therapeutic benefits on renal diseases associated with oxidative stress. This work was supported by National Natural Science Foundation of China (81170246 & 30973522) and Shanghai Pujiang Talents Program (11PJ1408300).

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