Effect of <i>Theobroma cacao</i> L. on the Efficacy and Toxicity of Doxorubicin in Mice Bearing Ehrlich Ascites Carcinoma

Background and objective: Doxorubicin is a widely used chemotherapeutic agent that causes oxidative stress leading to cardiotoxicity, hepatotoxicity, and nephrotoxicity. In contrast, <i>Theobroma cacao</i> L. has been recorded as an anticancer agent and found to be protective against mul...

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Main Authors: Priyanka P. Patil (Author), Pukar Khanal (Author), Vishal S. Patil (Author), Rajitha Charla (Author), Darasaguppe R. Harish (Author), Basanagouda M. Patil (Author), Subarna Roy (Author)
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Published: MDPI AG, 2022-05-01T00:00:00Z.
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042 |a dc 
100 1 0 |a Priyanka P. Patil  |e author 
700 1 0 |a Pukar Khanal  |e author 
700 1 0 |a Vishal S. Patil  |e author 
700 1 0 |a Rajitha Charla  |e author 
700 1 0 |a Darasaguppe R. Harish  |e author 
700 1 0 |a Basanagouda M. Patil  |e author 
700 1 0 |a Subarna Roy  |e author 
245 0 0 |a Effect of <i>Theobroma cacao</i> L. on the Efficacy and Toxicity of Doxorubicin in Mice Bearing Ehrlich Ascites Carcinoma 
260 |b MDPI AG,   |c 2022-05-01T00:00:00Z. 
500 |a 10.3390/antiox11061094 
500 |a 2076-3921 
520 |a Background and objective: Doxorubicin is a widely used chemotherapeutic agent that causes oxidative stress leading to cardiotoxicity, hepatotoxicity, and nephrotoxicity. In contrast, <i>Theobroma cacao</i> L. has been recorded as an anticancer agent and found to be protective against multiple chemical-induced organ injuries, including heart, liver, and kidney injuries. The present study investigated the possible role of extracts from <i>T. cacao</i> beans for organ-protective effects in doxorubicin-induced toxicity in mice bearing Ehrlich ascites carcinoma (EAC). Methodology: After survival analysis in rodents, cocoa bean extract (COE) was investigated for its efficacy against EAC-induced carcinoma and its organ-protective effect against doxorubicin-treated mice with EAC-induced carcinoma. Results: Significant reductions in EAC and doxorubicin-induced alterations were observed in mice administered the COE, either alone or in combination with doxorubicin. Furthermore, COE treatment significantly increased the mouse survival time, life span percentage, and antioxidant defense system. It also significantly improved cardiac, hepatic, and renal function biomarkers and markers for oxidative stress, and it also reduced doxorubicin-induced histopathological changes. Conclusion: COE acted against doxorubicin-induced organ toxicity; potent antioxidant and anticancer activities were also reflected by the COE itself. The COE may therefore serve as an adjuvant nutraceutical in cancer chemotherapy. 
546 |a EN 
690 |a anticancer 
690 |a cardiotoxicity 
690 |a cocoa 
690 |a doxorubicin 
690 |a Ehrlich ascites carcinoma 
690 |a <i>Theobroma cacao</i> L. 
690 |a Therapeutics. Pharmacology 
690 |a RM1-950 
655 7 |a article  |2 local 
786 0 |n Antioxidants, Vol 11, Iss 6, p 1094 (2022) 
787 0 |n https://www.mdpi.com/2076-3921/11/6/1094 
787 0 |n https://doaj.org/toc/2076-3921 
856 4 1 |u https://doaj.org/article/1b9fab8aab3b40b6a96758091492c9c8  |z Connect to this object online.