Phosphorylated PKM2 regulates endothelium-dependent vasodilation in diabetes.
10.11817/j.issn.1672-7347.2023.220541
- Author:
Bin LU
1
;
Lei TANG
2
;
Le LI
3
;
Xiaoyu ZHOU
2
;
Yiping LENG
4
;
Chengxuan QUAN
5
Author Information
1. Vascular Disease and Transformation Medical Center, Third Xiangya Hospital, Central South University, Changsha 410013. 18826401647@163.com.
2. Vascular Disease and Transformation Medical Center, Third Xiangya Hospital, Central South University, Changsha 410013.
3. Department of Cardiology, Affiliated Hospital of Southwest Medical University, Luzhou Sichuan 646000.
4. Research Center for Phase Ⅰ Clinical Trials, Affiliated Changsha Central Hospital, University of South China, Changsha 410004.
5. Vascular Disease and Transformation Medical Center, Third Xiangya Hospital, Central South University, Changsha 410013. 554723829@qq.com.
- Publication Type:Journal Article
- Keywords:
diabetes;
endothelial nitric oxide synthase;
endothelium-dependent vasodilation;
nitric oxide;
pyruvate kinase isozyme type M2
- MeSH:
Animals;
Humans;
Mice;
Carboxymethylcellulose Sodium/pharmacology*;
Diabetes Mellitus, Type 2/metabolism*;
Endothelium, Vascular/metabolism*;
Glucose/metabolism*;
Human Umbilical Vein Endothelial Cells;
Mice, Inbred C57BL;
Nitric Oxide/metabolism*;
Nitric Oxide Synthase Type III/metabolism*;
Phosphorylation;
Pyruvate Kinase/metabolism*;
Vasodilation
- From:
Journal of Central South University(Medical Sciences)
2023;48(5):663-670
- CountryChina
- Language:English
-
Abstract:
OBJECTIVES:Endothelium-dependent vasodilation dysfunction is the pathological basis of diabetic macroangiopathy. The utilization and adaptation of endothelial cells to high glucose determine the functional status of endothelial cells. Glycolysis pathway is the major energy source for endothelial cells. Abnormal glycolysis plays an important role in endothelium-dependent vasodilation dysfunction induced by high glucose. Pyruvate kinase isozyme type M2 (PKM2) is one of key enzymes in glycolysis pathway, phosphorylation of PKM2 can reduce the activity of pyruvate kinase and affect the glycolysis process of glucose. TEPP-46 can stabilize PKM2 in its tetramer form, reducing its dimer formation and phosphorylation. Using TEPP-46 as a tool drug to inhibit PKM2 phosphorylation, this study aims to explore the impact and potential mechanism of phosphorylated PKM2 (p-PKM2) on endothelial dependent vasodilation function in high glucose, and to provide a theoretical basis for finding new intervention targets for diabetic macroangiopathy.
METHODS:The mice were divided into 3 groups: a wild-type (WT) group (a control group, C57BL/6 mice) and a db/db group (a diabetic group, db/db mice), which were treated with the sodium carboxymethyl cellulose solution (solvent) by gavage once a day, and a TEPP-46 group (a treatment group, db/db mice+TEPP-46), which was gavaged with TEPP-46 (30 mg/kg) and sodium carboxymethyl cellulose solution once a day. After 12 weeks of treatment, the levels of p-PKM2 and PKM2 protein in thoracic aortas, plasma nitric oxide (NO) level and endothelium-dependent vasodilation function of thoracic aortas were detected. High glucose (30 mmol/L) with or without TEPP-46 (10 μmol/L), mannitol incubating human umbilical vein endothelial cells (HUVECs) for 72 hours, respectively. The level of NO in supernatant, the content of NO in cells, and the levels of p-PKM2 and PKM2 protein were detected. Finally, the effect of TEPP-46 on endothelial nitric oxide synthase (eNOS) phosphorylation was detected at the cellular and animal levels.
RESULTS:Compared with the control group, the levels of p-PKM2 in thoracic aortas of the diabetic group increased (P<0.05). The responsiveness of thoracic aortas in the diabetic group to acetylcholine (ACh) was 47% lower than that in the control group (P<0.05), and that in TEPP-46 treatment group was 28% higher than that in the diabetic group (P<0.05), while there was no statistically significant difference in the responsiveness of thoracic aortas to sodium nitroprusside (SNP). Compared with the control group, the plasma NO level of mice decreased in the diabetic group, while compared with the diabetic group, the phosphorylation of PKM2 in thoracic aortas decreased and the plasma NO level increased in the TEPP-46 group (both P<0.05). High glucose instead of mannitol induced the increase of PKM2 phosphorylation in HUVECs and reduced the level of NO in supernatant (both P<0.05). HUVECs incubated with TEPP-46 and high glucose reversed the reduction of NO production and secretion induced by high glucose while inhibiting PKM2 phosphorylation (both P<0.05). At the cellular and animal levels, TEPP-46 reversed the decrease of eNOS (ser1177) phosphorylation induced by high glucose (both P<0.05).
CONCLUSIONS:p-PKM2 may be involved in the process of endothelium-dependent vasodilation dysfunction in Type 2 diabetes by inhibiting p-eNOS (ser1177)/NO pathway.
