Role of Salvia hispanica seeds extract on Ehrlich ascites model induced liver damage in female mice | ||||
| Journal of Bioscience and Applied Research | ||||
| Articles in Press, Accepted Manuscript, Available Online from 02 May 2024 | ||||
| Document Type: Original Article | ||||
| DOI: 10.21608/jbaar.2024.274518.1040 | ||||
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| Authors | ||||
Ahmed Flayyih Hasan   1; Noor Adel Jasim1; Manar talib suhail2; Ali Talib Abid1; Ehab Tousson3
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| 1Biotechnology Research Center, Al-Nahrain University, Baghdad, Iraq. | ||||
| 2College of Science , Al-Nahrain University, Baghdad, Iraq. | ||||
| 3Zoology department, faculty of science, Tanta university | ||||
| Abstract | ||||
| Because the Ehrlich ascites carcinoma (EAC) model can accurately predict survival time and is successful in creating neoplastic cells, it is frequently employed in experimental cancer studies. The present work is designed to investigate The antitumorous properties and therapeutic potential of Chia (Salvia hispanica) seeds extract (ChSE) in inhibition of EAC induces liver toxicity and tissue injury. All is all of Forty female swiss albino mice were equally separated into four cohorts (Gp1, control group; Gp2, CHSE group; Gp3, EAC group; Gp4, EAC+ChSE). Current results revealed that; EAC caused a notable increase in serum Aspartate aminotransferase (ALT), alanine aminotransferase (AST),alkaline phosphatase (ALP) activities, body weight, liver weight, liver injury and a significant depletion in albumin and total proteins as in contrast to the control Gp. Post treatment of EAC with CHSE (EAC+ChSE) induced a significant depletion in serum ALT ,AST ,ALP , body weight, liver weight, liver injury and a notable rise in albumin and total proteins as compared to EAC Gp. One may draw the conclusion that ChSE possesses the capacity liver protective effect against EAC cells induced liver injury and signposts about the potential benefits of ChSE in the treatment of liver toxicity. | ||||
| Keywords | ||||
| Keywords : Ehrlich Ascites Carcinoma; Salvia hispanica; liver functions and structure; mice | ||||
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