Berberine attenuates inflammation and oxidative stress and modulates lymphocyte E-NTPDase in acute hyperlipidemia

被引:1
|
作者
Alruhaimi, Reem S. [1 ]
Siddiq Abduh, Maisa [2 ,3 ]
Ahmeda, Ahmad F. [4 ,5 ]
Bin-Ammar, Albandari [6 ]
Kamel, Emadeldin M. [7 ]
Hassanein, Emad H. M. [8 ]
Li, Chen [9 ]
Mahmoud, Ayman M. [10 ,11 ]
机构
[1] Princess Nourah bint Abdulrahman Univ, Coll Sci, Dept Biol, Riyadh, Saudi Arabia
[2] King Abdulaziz Univ, Fac Appl Med Sci, Dept Med Lab Sci, Immune Responses Different Dis Res Grp, Jeddah, Saudi Arabia
[3] King Abdulaziz Univ, Ctr Excellence Genom Med Res, Jeddah, Saudi Arabia
[4] Ajman Univ, Coll Med, Dept Basic Med Sci, Ajman, U Arab Emirates
[5] Ajman Univ, Ctr Med & Bioallied Hlth Sci Res, Ajman, U Arab Emirates
[6] Univ Hail, Coll Appl Med Sci, Dept Clin Nutr, Hail, Saudi Arabia
[7] Beni Suef Univ, Fac Sci, Chem Dept, Bani Suwayf, Egypt
[8] Al Azhar Univ, Fac Pharm, Dept Pharmacol & Toxicol, Assiut Branch, Assiut, Egypt
[9] Free Univ Berlin, Dept Biol, Chem, Pharm, Berlin, Germany
[10] Manchester Metropolitan Univ, Fac Sci & Engn, Dept Life Sci, Manchester M1 5GD, England
[11] Beni Suef Univ, Fac Sci, Zool Dept, Physiol Div, Bani Suwayf, Egypt
关键词
berberine; dyslipidemia; E-NTPDase; inflammation; oxidative stress; LOW-DENSITY-LIPOPROTEIN; LIPID-METABOLISM; ENDOTHELIAL-CELLS; CHOLESTEROL; MECHANISMS; MICE; ABSORPTION; INHIBITION; EXPRESSION; SECRETION;
D O I
10.1002/ddr.22166
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Hyperlipidemia is a common clinically encountered health condition worldwide that promotes the development and progression of cardiovascular diseases, including atherosclerosis. Berberine (BBR) is a natural product with acknowledged anti-inflammatory, antioxidant, and metabolic effects. This study evaluated the effect of BBR on lipid alterations, oxidative stress, and inflammatory response in rats with acute hyperlipidemia induced by poloxamer-407 (P-407). Rats were pretreated with BBR (25 and 50 mg/kg) for 14 days and acute hyperlipidemia was induced by a single dose of P-407 (500 mg/kg). BBR ameliorated hypercholesterolemia, hypertriglyceridemia, and plasma lipoproteins in P-407-adminsitered rats. Plasma lipoprotein lipase (LPL) activity was decreased, and hepatic 3-hydroxy-3-methylglutaryl CoA (HMG-CoA) reductase activity was enhanced in hyperlipidemic rats. The expression of low-density lipoprotein receptor (LDL-R) and ATP-binding cassette transporter 1 (ABCA1) was downregulated in hyperlipidemic rats. BBR enhanced LPL activity, upregulated LDL-R, and ABCA1, and suppressed HMG-CoA reductase in P-407-administered rats. Pretreatment with BBR ameliorated lipid peroxidation, nitric oxide (NO), pro-inflammatory mediators (interleukin [IL]-6, IL-1 beta, tumor necrosis factor [TNF]-alpha, interferon-gamma, IL-4 and IL-18) and enhanced antioxidants. In addition, BBR suppressed lymphocyte ecto-nucleoside triphosphate diphosphohydrolase (E-NTPDase) and ecto-adenosine deaminase (E-ADA) as well as NO and TNF-alpha release by macrophages isolated from normal and hyperlipidemic rats. In silico investigations revealed the binding affinity of BBR toward LPL, HMG-CoA reductase, LDL-R, PSK9, ABCA1, and E-NTPDase. In conclusion, BBR effectively prevented acute hyperlipidemia and its associated inflammatory responses by modulating LPL, cholesterolgenesis, cytokine release, and lymphocyte E-NTPDase and E-ADA. Therefore, BBR is an effective and safe natural compound that might be employed as an adjuvant against hyperlipidemia and its associated inflammation.
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页数:16
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