Evaluation of hypolipidemic Marrubium vulgare effect in Triton WR-1339 induced hyperlipidemia in mice
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作者:
Ibrahim, Abeer Y.
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Natl Res Ctr, Med & Aromat Plants Res Dept, Pharmaceut & Drug Ind Div, Cairo 12622, EgyptNatl Res Ctr, Med & Aromat Plants Res Dept, Pharmaceut & Drug Ind Div, Cairo 12622, Egypt
Ibrahim, Abeer Y.
[1
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Hendawy, Saber F.
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Natl Res Ctr, Med & Aromat Plants Res Dept, Pharmaceut & Drug Ind Div, Cairo 12622, EgyptNatl Res Ctr, Med & Aromat Plants Res Dept, Pharmaceut & Drug Ind Div, Cairo 12622, Egypt
Hendawy, Saber F.
[1
]
Elsayed, Ahmed A. A.
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Natl Res Ctr, Med & Aromat Plants Res Dept, Pharmaceut & Drug Ind Div, Cairo 12622, EgyptNatl Res Ctr, Med & Aromat Plants Res Dept, Pharmaceut & Drug Ind Div, Cairo 12622, Egypt
Elsayed, Ahmed A. A.
[1
]
Omer, Elsayed A.
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Natl Res Ctr, Med & Aromat Plants Res Dept, Pharmaceut & Drug Ind Div, Cairo 12622, EgyptNatl Res Ctr, Med & Aromat Plants Res Dept, Pharmaceut & Drug Ind Div, Cairo 12622, Egypt
Omer, Elsayed A.
[1
]
机构:
[1] Natl Res Ctr, Med & Aromat Plants Res Dept, Pharmaceut & Drug Ind Div, Cairo 12622, Egypt
Objective: To evaluate the hypocholesterolemic and hypotriglyceridemic activities of four Marrbium vulgare (M. vulgare) herb extracts using Triton WR-1339-induced hyperlipidemia in mice. Methods: Hyperlipidemia was developed by intraperitoneal injection of Triton (200 mg/kg body weight). The animals were divided into main four groups of eight mice each: normal control group, hyperlipidemic control group, hyperlipidemic plus tween-40 control and treated group. The fourth one was divided into four subgroups, petroleum ether extract group, chloroform extract group, ethyl acetate extract group and methanol extract treated group each of them contains two sub-sub group for treating animals with two doses at 0.1 and 0.25 LD50. Results: After 7 h and 24 h of treatment, the intragastric administration of all extracts caused a significant decrease of plasma total cholesterol. Triglyceride levels were also significantly lowered by all extracts while petroleum ether produced the lowest decreasing level. Similar results were observed for LDL-cholesterol concentrations. Furthermore, more polar extracts (methanol and ethyl acetate)-soluble fractions showed a significant ameliorative action on elevated atherogenic index (AI) and LDL/HDL-C ratios, while these atherogenic markers were not statistically suppressed by the chloroform and petroleum ether -soluble extract. Conclusion: The findings indicated that Marrubium may contain polar products able to lower plasma lipid concentrations and might be beneficial in treatment of hyperlipidemia and atherosclerosis.
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Department of Biotechnology, K.S.Rangasamy College of TechnologyDepartment of Biotechnology, K.S.Rangasamy College of Technology
Sidhra Syed Zameer Ahmed
Syed Zameer Ahmed Khader
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Department of Biotechnology, K.S.Rangasamy College of TechnologyDepartment of Biotechnology, K.S.Rangasamy College of Technology
Syed Zameer Ahmed Khader
Krishnaveni Radhakrishnan
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Department of Biotechnology, K.S.Rangasamy College of TechnologyDepartment of Biotechnology, K.S.Rangasamy College of Technology
Krishnaveni Radhakrishnan
Vanmathi Marimuthu
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Department of Biotechnology, K.S.Rangasamy College of TechnologyDepartment of Biotechnology, K.S.Rangasamy College of Technology
Vanmathi Marimuthu
Muniraj Chinnusamy
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Department of Electrical and Electronics Engineering, K.S.Rangasamy College of TechnologyDepartment of Biotechnology, K.S.Rangasamy College of Technology
Muniraj Chinnusamy
Venkatesan Thangavel
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Department of Electrical and Electronics Engineering, K.S.Rangasamy College of TechnologyDepartment of Biotechnology, K.S.Rangasamy College of Technology
Venkatesan Thangavel
Karamchand Ravi
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Department of Biotechnology, K.S.Rangasamy College of TechnologyDepartment of Biotechnology, K.S.Rangasamy College of Technology
Karamchand Ravi
Manimaran Vetrivel
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Department of Biotechnology, K.S.Rangasamy College of TechnologyDepartment of Biotechnology, K.S.Rangasamy College of Technology
机构:
King Abdulaziz Univ, Fac Pharm, Dept Pharmaceut, Jeddah, Saudi Arabia
Al Azhar Univ, Fac Pharm, Dept Pharmaceut & Ind Pharm, Cairo, EgyptKing Abdulaziz Univ, Fac Pharm, Dept Pharmaceut, Jeddah, Saudi Arabia
El-Say, Khalid M.
Ahmed, Tarek A.
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King Abdulaziz Univ, Fac Pharm, Dept Pharmaceut, Jeddah, Saudi Arabia
Al Azhar Univ, Fac Pharm, Dept Pharmaceut & Ind Pharm, Cairo, EgyptKing Abdulaziz Univ, Fac Pharm, Dept Pharmaceut, Jeddah, Saudi Arabia
Ahmed, Tarek A.
Ahmed, Osama A. A.
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King Abdulaziz Univ, Fac Pharm, Dept Pharmaceut, Jeddah, Saudi Arabia
Minia Univ, Fac Pharm, Dept Pharmaceut & Ind Pharm, Al Minya, EgyptKing Abdulaziz Univ, Fac Pharm, Dept Pharmaceut, Jeddah, Saudi Arabia
Ahmed, Osama A. A.
Elimam, Hanan
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Univ Sadat City, Fac Pharm, Dept Biochem, Monufia, EgyptKing Abdulaziz Univ, Fac Pharm, Dept Pharmaceut, Jeddah, Saudi Arabia