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Protective effect of Terminalia muelleri against carbon tetrachloride-induced hepato and nephro-toxicity in mice and characterization of its bioactive constituents.
Fahmy, Nouran Mohamed; Al-Sayed, Eman; Abdel-Daim, Mohamed M; Karonen, Maarit; Singab, Abdel Nasser.
  • Fahmy NM; a Department of Pharmacognosy , Faculty of Pharmacy, Ain-Shams University , Cairo , Egypt .
  • Al-Sayed E; a Department of Pharmacognosy , Faculty of Pharmacy, Ain-Shams University , Cairo , Egypt .
  • Abdel-Daim MM; b Department of Pharmacology , Faculty of Veterinary Medicine, Suez Canal University , Ismailia , Egypt , and.
  • Karonen M; c Laboratory of Organic Chemistry and Chemical Biology, Department of Chemistry , University of Turku , Turku , Finland.
  • Singab AN; a Department of Pharmacognosy , Faculty of Pharmacy, Ain-Shams University , Cairo , Egypt .
Pharm Biol ; 54(2): 303-13, 2016.
Article en En | MEDLINE | ID: mdl-25894213
ABSTRACT
CONTEXT Terminalia is used in folk medicine for the treatment of various diseases.

OBJECTIVE:

The objective of this study is to investigate the hepatonephro protective activity of a polyphenol-rich fraction (TMEF) obtained from Terminalia muelleri Benth. (Combretaceae) against CCl4-induced toxicity in mice. MATERIALS AND

METHODS:

TMEF was administered (100, 200, and 400 mg/kg/d) for 5 d. CCl4 was administered at the end of the experiment. Hepatic and renal biomarkers were measured in the serum. Glutathione (GSH), superoxide dismutase (SOD), and malondialdehyde (MDA) were estimated in the liver and kidney tissues. The active constituents of TMEF were identified by HPLC-PDA-ESI/MS/MS.

RESULTS:

TMEF is rich in ellagitannins, galloyl esters, phenolic acids, and flavone-C-glucosides. TMEF pretreatment significantly (p < 0.001) inhibited the CCl4-induced increase in ALT (17, 43, and 53%), AST (20, 46, and 58%), ALP (20, 48, and 56%), LDH (21, 47, and 58%), hepatic MDA (23, 49, and 54%), renal MDA (22, 35, and 52%), creatinine (48, 66, and 91%), uric acid (16, 34, and 59%), urea (22, 39, and 59%), and cholesterol (20, 27, and 46%). Furthermore, TMEF administration significantly (p < 0.001) increased hepatic GSH (15, 51, and 79%), renal GSH (23, 45, and 73%), hepatic SOD (9, 52, and 95%), renal SOD (39, 66, and 85%) and protein levels (17, 24, and 29%) at the tested doses of TMEF, respectively. Pretreatment with TMEF preserved the hepatic architecture and protected from ballooning degeneration, liver necrosis, renal inflammation, and degeneration of the kidney tubules.

CONCLUSION:

TMEF has a marked hepato-nephro protective effect.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Extractos Vegetales / Sustancias Protectoras / Terminalia / Enfermedad Hepática Inducida por Sustancias y Drogas / Polifenoles / Nefritis Límite: Animals Idioma: En Año: 2016 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Extractos Vegetales / Sustancias Protectoras / Terminalia / Enfermedad Hepática Inducida por Sustancias y Drogas / Polifenoles / Nefritis Límite: Animals Idioma: En Año: 2016 Tipo del documento: Article