Journal of Traditional Chinese Medicine >
Efficacy of Dangua Fang (丹瓜方) on endothelial cells damaged by oxidative stress
Received date: 2021-07-07
Accepted date: 2021-10-17
Online published: 2022-08-15
Supported by
Based on The "miR34a/Nampt-NAD+-TAC" Pathway to Study the Mechanism of Simultaneously Treating The Phlegm And Blood Stasis in The Regulation of Glycolipid(81873213);Study on the Mechanism of Simultaneously Treating the Phlegm and Blood Stasis on Glycolipid Metabolism Based on Intestinal Fat Absorption Regulated by miR-34a/Stat3-Nfil3 Pathway(82074308);Preparation of Monomeric Traditional Chinese Medicine Complexes Based on Nampt's Activation of Tricarboxylic Acid Cycle And Respiratory Chain to Interfere with Glycolipid Metabolism(2022Y41016)
OBJECTIVE: To evaluate the protective effects of serum containing Dangua Fang (丹瓜方) on vascular endothelium damaged by oxidative stress.
METHODS: Five experiments were completed in this paper. In the first experiment, we found the most suitable serum containing Dangua Fang by comparing groups with different serum containing Dangua Fang. In the second experiments we analyzed Dangua Fang influencing endothelial cell viability and apoptosis and cell cycle. The third experiment on Dangua Fang intervention of mitochondrial respiratory chain. The fourth experiment on Dangua Fang intervention of mitochondrial membrane potential. And finally, on the fifth experiment we researched the mechanism of Dangua Fang improving mitochondrial function by comparing the Na+-k+-ATPase and peroxisome proliferator-activated receptor- gamma coactivator-1alpha (PGC-1α) in the Dangua group with the diazoxide group and Co Q+Vit C group.
RESULTS: We compared the control group in the first experiments and the OD values in DZ1 group was the most significant in all intervening groups. The recipe of DZ1 (5% serum containing Dangua Fang) was used in the following experiments. Compared with the control group, cell viability, cell cycle (G2 + S), cytochrome c oxidase (COX), R3 red/green, R2 red/green, R1 red/ green decreased and apoptosis, succinate dehy-drogenase (SDH), green (R2 + R3), Na+-k+-ATPase, PGC-1α increased in the model group. Compared with the model group, cell viability, G2+S, COX, R3 red/green, R2 red/green, R1 red/green raised and apoptosis, green (R2 + R3), Na-K-ATPase decreased in the Dangua group; G2 + S, R3 red/green, R2 red/green, R1 red/green raised and green (R2 + R3) decreased in the Co Q + Vit C group. Na-K-ATPase increased in the combined group (P < 0.05 or < 0.01).
CONCLUSIONS: Dangua Fang protects oxidative stress-induced endothelial cells damaged by promotion of mitochondrial biogenesis, reduction of Na+-K+-ATPase activity and regulation of mitochondrial respiratory chain function restoring mitochondrial membrane potential.
Xianpei HENG , Liang LI , Liuqin YANG , Zhita WANG . Efficacy of Dangua Fang (丹瓜方) on endothelial cells damaged by oxidative stress[J]. Journal of Traditional Chinese Medicine, 2022 , 42(6) : 900 -907 . DOI: 10.19852/j.cnki.jtcm.20220815.001
| [1] | Heng XP, Yang LQ, Li L, Chen ML. Paradox of using intensive lowering of blood glucose in diabetics and strategies to overcome it and decrease cardiovascular risks. Chin J Integr Med 2015, 21: 425-34 |
| [2] | Heng XP, Li XJ, Li L, Yang LQ, Wang ZT. Therapy to obese Type 2 diabetes mellitus: how far will we go down the wrong road? Chin J Integr Med 2020, 26: 62-71. |
| [3] | Pistritto G, Trisciuoglio D, Ceci C, Garufi A, D'Orazi G. Apoptosis as anticancer mechanism: function and dysfunction of its modulators and targeted therapeutic strategies. Aging (Albany NY) 2016; 8: 603-19. |
| [4] | Chen L, Yang W, Guo Y, et al. Exosomal lncRNA GAS 5 regulates the apoptosis of macrophages and vascular endothelial cells in atherosclerosis. PLoS One 2017; 12: e0185406. |
| [5] | Watson EC, Grant ZL, Coultas L. Endothelial cell apoptosis in angiogenesis and vessel regression. Cell Mol Life Sci 2017; 74: 4387-403. |
| [6] | Lan YL, Huang XP, Heng XP, et al. Dangua Fang improves glycolipid metabolic disorders by promoting hepatic adenosine 5’-monophosphate activated protein kinase expression in diabetic Goto-Kakizaki rats. Chin J Integr Med 2015; 21: 188-95. |
| [7] | Huang SP, Kang WQ, Liu YJ, Huang BW, Shao JJ. Effects of Dangua formula on the protein expression of LKB1, AMPK and SIRT1 in liver of diabetic rats. Zhong Hua Zhong Yi Yao Za Zhi 2019; 34: 4003-7. |
| [8] | Heng XP, Huang SP, Cheng XL, et al. Research of Dangua recipe on intervening the glycolipid metabolism and oxidative stress in diabetic rats with atherosclerosis. Zhong Guo Zhong Xi Yi Jie He Za Zhi 2013; 33: 244-51. |
| [9] | Heng XP, Li L, Huang SP, et al. Effect of Dangua recipe on glycolipid metabolism and VCAM-1 and its mRNA expression level in Apo E (-/-) mice with diabetes mellitus. Zhong Guo Zhong Xi Yi Jie He Za Zhi 2014; 34: 1086-95. |
| [10] | Yang LQ, Li L, Heng XP, Huang SP, Pan XD. Effects of Dangua recipe on inflammeatory marders and endothelial cell function in diabetic rats with arteriosclerosis. Zhong Guo Zhong Xi Yi Jie He Za Zhi 2017, 37: 692-8. |
| [11] | Xu RX, Wang ZT, Cheng YC, et al. Effects of Dangua recipe on myocardial ATP, PPARα, GLUT-4,and morphology in diabetic rats. Zhong Guo Zhong Xi Yi Jie He Za Zhi 2018; 38: 1363-8. |
| [12] | Chen YC, Li L, Heng XP, et al. Effects of Dangua recipe on expression leveis of caspase-3 protein, Bcl-2 and Bax mRNA in brain tissue of Apo E-/- diabetes model mice. Zhong Guo Zhong Xi Yi Jie He Za Zhi 2017; 37: 1476-81. |
| [13] | Heng XP, Yang LQ, Li L, Pan XD, Huang SP. Dangua recipe regulates protein and mRNA expression of p38-MAPK, MCP-1 and FN in renal of Apo E-/-murine model of diabetes. Zhong Guo Zhong Xi Yi Jie He Za Zhi 2018; 39: 459-65. |
| [14] | Heng XP, Yang LQ, Huang SP, et al. A Clinical study of Danggua Humai oral liquid on cardiovascular risk factors among patients with type 2 diabetes mellitus. Zhong Guo Zhong Xi Yi Jie He Za Zhi 2019; 39: 275-81. |
| [15] | Heng XP, Chen KJ, Hong ZF, et al. Glucose endothelial cytotoxicity and protection of Dan Gua-Fang, a Chinese herb prescription in huVEC in hyperglycemia medium. J Diabetes Complications 2009, 23: 297-303. |
| [16] | Heng XP, Chen KJ, Hong ZF, et al. Toxicity features of high glucose on endothelial cell cycle and protection by Dan Gua-Fang in ECV-304 in high glucose medium. Chin J Integr Med. 2013, 19: 596-602. |
| [17] | Gu MX, Wang J, Wang Y, et al. MiR-147b inhibits cell viability and promotes apoptosis of rat H9c2 cardiomyocytes via down-regulating KLF13 expression. Acta Biochim Biophys Sin (Shanghai) 2018; 50: 288-97. |
| [18] | Liao GL, Ma L, Zeng T. The effects medlar flavone on no and NOS in H2O2damaged vascular endothelial cell. Chong Qin Yi Xue 2015, 44: 3323-27 |
| [19] | Tian G, Liu ZQ, Yuan ZY. Membrance phospholipids injury in myocardia cells of adriamycin rats and the protective effects of CoQ10 on it. Xi An Yi Ke Da Xue Xue Bao 1997, 18: 329-33 |
| [20] | Cropper JR, Hicks M, Ryan JB, Macdonald PS. Enhanced cardioprotection of the rat heart during hypothermic storage with combined Na+ - H+ exchange inhibition and ATP-dependent potassium channel activation. J Heart Lung Transplant World J Tradit Chin Med 2003; 22: 1245-53. |
| [21] | Wada J, Nakatsuka A. Mitochondrial dynamics and mitochondrial dysfunction in diabetes. Acta Med Okayama 2016; 70: 151-8. |
| [22] | Rocha M, Diaz-Morales N, Rovira-Llopis S, et al. Mitochondrial dysfunction and endoplasmic reticulum stress in diabetes. Curr Pharm Des 2016; 22: 2640-9. |
| [23] | Gu XL.MicroRNA-124 prevents H2O2-induced apoptosis and oxidative stress in human lens epithelial cells via inhibition of the NF-κB signaling pathway. Pharmacology 2018; 102: 213-22. |
| [24] | Holvoet P, Vanhaverbeke M, Geeraert B, De Keyzer D, Hulsmans M, Janssens S. Low cytochrome oxidase 1 links mitochondrial dysfu nction to atherosclerosis in mice and pigs. PLoS One 2017; 12: e0170307. |
| [25] | Sarparanta J, García-Macia M, Singh R.Autophagy and mitochondria in obesity and type 2 diabetes. Curr Diabetes Rev 2017; 13: 352-9. |
| [26] | Kogot-Levin A, Saada A, Leibowitz G, et al. Upregulation of mitochondrial content in cytochrome c oxidase deficient fibroblasts. PLoS One 2016; 11: e0165417. |
| [27] | De La Fuente S, Lambert JP, Nichtova Z, et al. Spatial separation of mitochondrial calcium uptake and extrusion for energy-efficient mitochondrial calcium signaling in the heart. Cell Rep 2018; 24: 3099- 107. e4. |
| [28] | Li PA, Hou X, Hao S. Mitochondrial biogenesis in neurodegeneration. J Neurosci Res 2017; 95: 2025-9. |
| [29] | Heng XP, Wang ZT, Li L, Yang LQ, Huang SP. Mechanisms of Dangua recipe in improving glycolipid metabolic disorders based on transcriptomics. Chin J Integr Med 2022; 28: 130-7. |
| [30] | Cantó C, Auwerx J. PGC-1alpha, SIRT1 and AMPK, an energy sensing network that controls energy expenditure. Curr Opin Lipidol 2009; 20: 98-105. |
| [31] | Tang BL. Sirt1 and the mitochondria. Mol Cells 2016; 39: 87-95. |
| [32] | Shaw RJ, Lamia KA, Vasquez D, et al. The kinase LKB1 mediates glucose homeostasis in liver and therapeutic effects of metformin. Science 2005; 310: 1642-6. |
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