Hepatoprotective effect of a polyherbal formulation (Aab-e-Murawaqain) against CCl4 induced liver toxicity in Wistar albino rat model by suppressing proinflammatory cytokines

被引:7
作者
Amir, Mohd [1 ]
Ahmad, Wasim [2 ]
Sarafroz, Mohammad [3 ]
Ahmad, Ajaz [4 ]
Ali, Abuzer [5 ]
Ansari, Mohammad Azam [6 ]
Thiruvengadam, Muthu [7 ]
Wahab, Shadma [8 ]
Ashraf, Kamran [9 ]
Barkat, Abul [10 ]
Mujeeb, Mohd [11 ]
机构
[1] Imam Abdulrahman Bin Faisal Univ, Coll Clin Pharm, Dept Nat Prod & Alternat Med, 1982, Dammam, Saudi Arabia
[2] Mohammed Al Mana Coll Med Sci, Dept Pharm, Dammam 34222, Saudi Arabia
[3] Imam Abdulrahman Bin Faisal Univ, Coll Clin Pharm, Dept Pharmaceut Chem, 1982, Dammam, Saudi Arabia
[4] King Saud Univ, Coll Pharm, Dept Clin Pharm, Riyadh 11451, Saudi Arabia
[5] Taif Univ, Coll Pharm, Dept Pharmacognosy, POB 11099, Taif 21944, Saudi Arabia
[6] Imam Abdulrahman Bin Faisal Univ, Inst Res & Med Consultat IRMC, Dept Epidem Dis Res, Dammam 31441, Saudi Arabia
[7] Konkuk Univ, Coll Life & Environm Sci, Dept Appl Biosci, Seoul 05029, Saudi Arabia
[8] King Khalid Univ, Coll Pharm, Dept Pharmacognosy, Abha, Saudi Arabia
[9] Univ Teknol MARA, UiTM, Fac Pharm, Kampus Puncak Alam, Seleangor Darul Ehsan 42300, Malaysia
[10] Univ Hafr Al Batin, Coll Pharm, Dept Pharmaceut, Hafar al Batin 35924, Saudi Arabia
[11] Sch Pharmaceut Educ & Res, Dept Pharmacognosy & Phytochem, Jamia Hamdard 62, New Delhi, India
关键词
Aab-e-Murawaqain; Hepatoprotective; Solanum nigrum; Cichorium intybus; Proin flammatory cytokines; DIOSGENIN; ANTIOXIDANT; INJURY; DAMAGE;
D O I
10.1016/j.sajb.2021.11.020
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
This study assessed the hepatoprotective action of Aab-e-Murawaqain in Wistar albino rats by inducing liver injury with carbon tetrachloride (CCl4) (2 mL/kg; sc). Aqueous extracts of Solanum nigrum (Makoy) and Cicho-rium intybus (Kashni) were used to prepare the Aab-e-Murawaqain polyherbal formulation. Silymarin (25 mg/kg), a well-known liver protective medicine, was treated as the reference control group. Biochemical indicators, such as serum glutamate oxaloacetate transaminase (SGOT), serum glutamate pyruvate transami-nase (SGPT), alkaline phosphatase (ALP), and total bilirubin, were used to assess the curative potential. Other common biomarkers, such as thiobarbituric acid reactive substances (TBARS), superoxide dismutase (SOD), glutathione (GSH), and catalase (CAT), were also estimated. Animals treated with CCl4 exhibited significantly enhanced in SGOT, SGPT, ALP, bilirubin, and TBARS level, reflecting hepatic damage. The formulation consid-erably minimised the increase serum enzyme levels, indicating the improvement in liver cellular injury. CCl4 induced significant decrease in GSH, SOD, and CAT levels. Pretreatment of the rats with the formulation led to an increase in hepatic GSH, SOD, CAT, protein, and albumin levels. Moreover, CCl4 administration led to an increase in TNF-a, IL-6, and IL-10 levels, which decreased with polyherbal formulation treatment. The results were validated through histological evolutions, which revealed minimum fatty variations and a noticeable regenerative effect in the livers after treatment with the formulation. The results confirmed that Aab-e-Mur-awaqain can provide a substantial activity in the management of CCl4-induced hepatotoxicity.(c) 2021 SAAB. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:75 / 81
页数:7
相关论文
共 48 条
[1]   Antioxidant, antimicrobial and cytotoxic activities of selected medicinal plants from Yemen [J].
Al-Fatimi, Mohamed ;
Wurster, Martina ;
Schroeder, Gudrun ;
Lindequist, Ulrike .
JOURNAL OF ETHNOPHARMACOLOGY, 2007, 111 (03) :657-666
[2]  
[Anonymous], 2011, OECD Guidelines for the Testing of Chemicals, V1, P1
[3]  
[Anonymous], 1975, INDIAN J PHARMACOL
[4]  
[Anonymous], 2003, WHO Technical Report Series, V916
[5]  
Arzani A, 1938, QARABADEEN E QADRI, P453
[6]   PRELIMINARY PHYTOCHEMICAL AND PHARMACOLOGICAL INVESTIGATIONS OF ROOTS OF DIFFERENT VARIETIES OF CICHORIUM-INTYBUS [J].
BALBAA, SI ;
ZAKI, AY ;
ABDELWAH.SM ;
ELDENSHA.ES ;
MOTAZZBE.M .
PLANTA MEDICA, 1973, 24 (02) :133-144
[7]   Glutathione dysregulation and the etiology and progression of human diseases [J].
Ballatori, Nazzareno ;
Krance, Suzanne M. ;
Notenboom, Sylvia ;
Shi, Shujie ;
Tieu, Kim ;
Hammond, Christine L. .
BIOLOGICAL CHEMISTRY, 2009, 390 (03) :191-214
[8]  
Bayaz-e-Kabeer, 1921, BAYAZ E KABEER 3, P8
[9]  
Claiborne A., 1985, CRC Handbook of Methods for Oxygen Radical Research, DOI DOI 10.1016/0531-5565(85)90021-X
[10]   Liv.52 in alcoholic liver disease: a prospective, controlled trial [J].
de Silva, HA ;
Saparamadu, PAM ;
Thabrewc, MI ;
Pathmeswaran, A ;
Fonseka, MMD ;
de Silva, HJ .
JOURNAL OF ETHNOPHARMACOLOGY, 2003, 84 (01) :47-50