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Toxicity effects of oral administration of clinacanthus nutans ethanolic leaf extract on blood, liver and kidneys of mice

By: Aliyu, A.
Contributor(s): Shaari, M. R.
Publisher: Mumbai Indian Journal of Pharmaceutical Science 2021Edition: Vol.83(6), Nov-Dec.Description: 1181-1195p.Subject(s): PHARMACEUTICSOnline resources: Click here In: Indian journal of pharmaceutical sciencesSummary: Clinacanthus nutans has been used traditionally in the treatment of herpes simplex viral infection. This research evaluated the toxicity effects of sub-chronic oral administration of Clinacanthus nutans ethanolic leaf extract in Institute of Cancer Research mice. A total 50, 8 w old female mice were divided into five groups of 10 mice each; Group A (control), Group B (125 mg/kg), Group C (250 mg/kg), Group D (500 mg/kg) and Group E (1000 mg/kg). The extract was administered orally for 90 d. The mice were monitored and sacrificed on d 91. Blood, liver and kidney samples were collected for analyses. There was significant (p<0.05) alterations in the haematological parameters of the mice in Group E and a significant increase in creatinine levels in groups B, C, D and E compared to A. The plasma level of alanine aminotransferase was significantly (p<0.05) higher in Groups D and E, compared to A. Histopathological evaluation of liver and kidneys revealed a moderate cytoplasmic vacuolation, eosinophilic cytoplasm and pyknosis of hepatocytes, as well as mild to moderate activated Kupffer cells in Group E. Similarly, the renal tubular cells showed mild to moderate renal cytoplasmic vacuolation, eosinophilic cytoplasm, pyknotic and karyolytic cells in Group E. It is concluded that repeated oral doses of Clinacanthus nutans ethanolic leaf extract for 90 d induced hepato-renal toxicities in female Institute of Cancer Research mice.
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Clinacanthus nutans has been used traditionally in the treatment of herpes simplex viral infection. This
research evaluated the toxicity effects of sub-chronic oral administration of Clinacanthus nutans ethanolic
leaf extract in Institute of Cancer Research mice. A total 50, 8 w old female mice were divided into
five groups of 10 mice each; Group A (control), Group B (125 mg/kg), Group C (250 mg/kg), Group D
(500 mg/kg) and Group E (1000 mg/kg). The extract was administered orally for 90 d. The mice were
monitored and sacrificed on d 91. Blood, liver and kidney samples were collected for analyses. There
was significant (p<0.05) alterations in the haematological parameters of the mice in Group E and a
significant increase in creatinine levels in groups B, C, D and E compared to A. The plasma level of alanine
aminotransferase was significantly (p<0.05) higher in Groups D and E, compared to A. Histopathological
evaluation of liver and kidneys revealed a moderate cytoplasmic vacuolation, eosinophilic cytoplasm
and pyknosis of hepatocytes, as well as mild to moderate activated Kupffer cells in Group E. Similarly,
the renal tubular cells showed mild to moderate renal cytoplasmic vacuolation, eosinophilic cytoplasm,
pyknotic and karyolytic cells in Group E. It is concluded that repeated oral doses of Clinacanthus nutans
ethanolic leaf extract for 90 d induced hepato-renal toxicities in female Institute of Cancer Research mice.

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