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Protective effect of some natural products against chemotherapy-induced toxicity in rats

AIM: There is a great interest in combining anticancer drugs with natural products aiming at maximizing their efficacy while minimizing systemic toxicity. Hence, the present study was constructed aiming to investigate the protective potential of three natural products, 1,8-cineole an essential oil f...

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Autores principales: Abdallah, Heba M.I., Abdel-Rahman, Rehab F., El Awdan, Sally A., Allam, Rasha M., El-Mosallamy, Aliaa E.M.K., Selim, Manal S., Mohamed, Sahar S., Arbid, Mahmoud S., Farrag, Abdel Razik H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507045/
https://www.ncbi.nlm.nih.gov/pubmed/31080906
http://dx.doi.org/10.1016/j.heliyon.2019.e01590
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author Abdallah, Heba M.I.
Abdel-Rahman, Rehab F.
El Awdan, Sally A.
Allam, Rasha M.
El-Mosallamy, Aliaa E.M.K.
Selim, Manal S.
Mohamed, Sahar S.
Arbid, Mahmoud S.
Farrag, Abdel Razik H.
author_facet Abdallah, Heba M.I.
Abdel-Rahman, Rehab F.
El Awdan, Sally A.
Allam, Rasha M.
El-Mosallamy, Aliaa E.M.K.
Selim, Manal S.
Mohamed, Sahar S.
Arbid, Mahmoud S.
Farrag, Abdel Razik H.
author_sort Abdallah, Heba M.I.
collection PubMed
description AIM: There is a great interest in combining anticancer drugs with natural products aiming at maximizing their efficacy while minimizing systemic toxicity. Hence, the present study was constructed aiming to investigate the protective potential of three natural products, 1,8-cineole an essential oil from Artemisia herba alba, exopolysaccharide (EPS) from locally identified marine streptomycete, and ellagic acid (EA), against chemotherapy-induced organ toxicity. METHODS: Isolation, production and characterization of EPS from marine streptomycete was done. Animals were allocated into five groups, GP1: normal control, GP2: cyclophosphamide (CYC), GP3: 1,8-cineole + CYC, GP4: EPS + CYC, GP4: EA + CYC. All drugs were administered orally 1 week before and concomitantly with CYC. Electrocardiography (ECG) analysis, liver enzymes (ALT and AST), cardiac serum markers (LDH and CK), oxidative stress biomarkers in hepatic and cardiac tissues (GSH and MDA), TGF-β1 and histopathological examination of hepatic and cardiac tissues were executed. RESULTS: The isolated stain produced EPS was identified as Streptomyces xiamenensis. EPS contains uronic, sulphate groups and different monosugars with Mw 4.65 × 10(4) g/mol and showed antioxidant activity against DPPH. Pretreatment of rats with 1,8-cineole, EPS and EA improved ECG abnormalities, decrease serum markers of hepato- and cardiotoxicity, prevent oxidative stress and decrease TGF-β1 in liver and heart tissues. CONCLUSION: The present results demonstrate the hepatoprotective and cardioprotective effects of the above-mentioned natural products against CYC organ toxicity.
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spelling pubmed-65070452019-05-10 Protective effect of some natural products against chemotherapy-induced toxicity in rats Abdallah, Heba M.I. Abdel-Rahman, Rehab F. El Awdan, Sally A. Allam, Rasha M. El-Mosallamy, Aliaa E.M.K. Selim, Manal S. Mohamed, Sahar S. Arbid, Mahmoud S. Farrag, Abdel Razik H. Heliyon Article AIM: There is a great interest in combining anticancer drugs with natural products aiming at maximizing their efficacy while minimizing systemic toxicity. Hence, the present study was constructed aiming to investigate the protective potential of three natural products, 1,8-cineole an essential oil from Artemisia herba alba, exopolysaccharide (EPS) from locally identified marine streptomycete, and ellagic acid (EA), against chemotherapy-induced organ toxicity. METHODS: Isolation, production and characterization of EPS from marine streptomycete was done. Animals were allocated into five groups, GP1: normal control, GP2: cyclophosphamide (CYC), GP3: 1,8-cineole + CYC, GP4: EPS + CYC, GP4: EA + CYC. All drugs were administered orally 1 week before and concomitantly with CYC. Electrocardiography (ECG) analysis, liver enzymes (ALT and AST), cardiac serum markers (LDH and CK), oxidative stress biomarkers in hepatic and cardiac tissues (GSH and MDA), TGF-β1 and histopathological examination of hepatic and cardiac tissues were executed. RESULTS: The isolated stain produced EPS was identified as Streptomyces xiamenensis. EPS contains uronic, sulphate groups and different monosugars with Mw 4.65 × 10(4) g/mol and showed antioxidant activity against DPPH. Pretreatment of rats with 1,8-cineole, EPS and EA improved ECG abnormalities, decrease serum markers of hepato- and cardiotoxicity, prevent oxidative stress and decrease TGF-β1 in liver and heart tissues. CONCLUSION: The present results demonstrate the hepatoprotective and cardioprotective effects of the above-mentioned natural products against CYC organ toxicity. Elsevier 2019-05-07 /pmc/articles/PMC6507045/ /pubmed/31080906 http://dx.doi.org/10.1016/j.heliyon.2019.e01590 Text en © 2019 Published by Elsevier Ltd. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Abdallah, Heba M.I.
Abdel-Rahman, Rehab F.
El Awdan, Sally A.
Allam, Rasha M.
El-Mosallamy, Aliaa E.M.K.
Selim, Manal S.
Mohamed, Sahar S.
Arbid, Mahmoud S.
Farrag, Abdel Razik H.
Protective effect of some natural products against chemotherapy-induced toxicity in rats
title Protective effect of some natural products against chemotherapy-induced toxicity in rats
title_full Protective effect of some natural products against chemotherapy-induced toxicity in rats
title_fullStr Protective effect of some natural products against chemotherapy-induced toxicity in rats
title_full_unstemmed Protective effect of some natural products against chemotherapy-induced toxicity in rats
title_short Protective effect of some natural products against chemotherapy-induced toxicity in rats
title_sort protective effect of some natural products against chemotherapy-induced toxicity in rats
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6507045/
https://www.ncbi.nlm.nih.gov/pubmed/31080906
http://dx.doi.org/10.1016/j.heliyon.2019.e01590
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