Low-dose nifedipine rescues impaired endothelial progenitor cell-mediated angiogenesis in diabetic mice

被引:0
|
作者
Cheng Peng
Li-jun Yang
Chuan Zhang
Yu Jiang
Liu-wen-xin Shang
Jia-bei He
Zhen-wei Zhou
Xia Tao
Lu Tie
Alex F. Chen
He-hui Xie
机构
[1] Shanghai Jiao Tong University School of Medicine,School of Public Health and Hongqiao International Institute of Medicine
[2] Shanghai Jiao Tong University School of Medicine,Institute for Developmental and Regenerative Cardiovascular Medicine, Xinhua Hospital
[3] Shanghai University,School of Medicine
[4] Second Affiliated Hospital of Naval Medical University,Department of Pharmacy
[5] Peking University and Beijing Key Laboratory of Tumor Systems Biology,Department of Pharmacology, School of Basic Medical Sciences
[6] Peking University,undefined
来源
Acta Pharmacologica Sinica | 2023年 / 44卷
关键词
diabetes; nifedipine; endothelial progenitor cells; angiogenesis; cerebral ischemia; thrombospondins;
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摘要
It is of great clinical significance to develop potential novel strategies to prevent diabetic cardiovascular complications. Endothelial progenitor cell (EPC) dysfunction is a key contributor to diabetic vascular complications. In the present study we evaluated whether low-dose nifedipine could rescue impaired EPC-mediated angiogenesis and prevent cardiovascular complications in diabetic mice. Diabetes was induced in mice by five consecutive injections of streptozotocin (STZ, 60 mg·kg−1·d−1, i.p.). Diabetic mice were treated with low-dose nifedipine (1.5 mg·kg−1·d−1, i.g.) for six weeks. Then, circulating EPCs in the peripheral blood were quantified, and bone marrow-derived EPCs (BM-EPCs) were prepared. We showed that administration of low-dose nifedipine significantly increased circulating EPCs, improved BM-EPCs function, promoted angiogenesis, and reduced the cerebral ischemic injury in diabetic mice. Furthermore, we found that low-dose nifedipine significantly increased endothelial nitric oxide synthase (eNOS) expression and intracellular NO levels, and decreased the levels of intracellular O2.− and thrombospondin-1/2 (TSP-1/2, a potent angiogenesis inhibitor) in BM-EPCs of diabetic mice. In cultured BM-EPCs, co-treatment with nifedipine (0.1, 1 μM) dose-dependently protected against high-glucose-induced impairment of migration, and suppressed high-glucose-induced TSP-1 secretion and superoxide overproduction. In mice with middle cerebral artery occlusion, intravenous injection of diabetic BM-EPCs treated with nifedipine displayed a greater ability to promote local angiogenesis and reduce cerebral ischemic injury compared to injection of diabetic BM-EPCs treated with vehicle, and the donor-derived BM-EPCs homed to the recipient ischemic brain. In conclusion, low-dose nifedipine can enhance EPCs’ angiogenic potential and protect against cerebral ischemic injury in diabetic mice. It is implied that chronic treatment with low-dose nifedipine may be a safe and economic manner to prevent ischemic diseases (including stroke) in diabetes.
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页码:44 / 57
页数:13
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