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Lyophilized equine platelet-rich plasma (L-GF(equina)) antagonize the Reproductive toxicity and oxidative stress Induced by Cyclophosphamide in female rats

BACKGROUND: The antineoplastic agent Cyclophosphamide (CP) induces reproductive toxicity. New strategies for protecting ovarian tissue damage in women with chemotherapy-induced reproductive toxicity are essential. This study was designed to evaluate the possible protective effect of combined treatme...

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Autores principales: Abdoon, Ahmed Sabry S., Al-Atrash, Ahmed M.E, Soliman, Seham S., El-Sanea, Amro M., Gamal el Din, Amina A., Fahmy, Hossam M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10141944/
https://www.ncbi.nlm.nih.gov/pubmed/37118826
http://dx.doi.org/10.1186/s13048-023-01161-x
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author Abdoon, Ahmed Sabry S.
Al-Atrash, Ahmed M.E
Soliman, Seham S.
El-Sanea, Amro M.
Gamal el Din, Amina A.
Fahmy, Hossam M.
author_facet Abdoon, Ahmed Sabry S.
Al-Atrash, Ahmed M.E
Soliman, Seham S.
El-Sanea, Amro M.
Gamal el Din, Amina A.
Fahmy, Hossam M.
author_sort Abdoon, Ahmed Sabry S.
collection PubMed
description BACKGROUND: The antineoplastic agent Cyclophosphamide (CP) induces reproductive toxicity. New strategies for protecting ovarian tissue damage in women with chemotherapy-induced reproductive toxicity are essential. This study was designed to evaluate the possible protective effect of combined treatment with L-GF(equina) on CP-induced reproductive toxicity in the mature female rat. METHODOLOGY: Forty mature female rats were assigned into four groups: First group, control: rats were intraperitoneally injected (IP) with 200 µl sterile saline solution on days 1 and 10; Group 2 (CP): were IP injected with 75 mg/kg on days 1 and 10 to induce POI); Group 3 (CP + L-GF(equina)): as in group 2 + IP injected with 200 µl rehydrated L-GF(equina) half-hour after CP injection on day 1 and 10); Group 4 (L-GF(equina)): rats were IP injected with 200 µl L-GF(equina) on day 1 and 10). Blood samples were collected for a complete blood picture and determinations of nitric oxide and malondialdehyde. Animals were sacrificed on Day-21, and genitalia was dissected, weighed, and fixed in 10% formalin for histopathological and morphometric evaluation. RESULTS: On day 21 of the experiment, body weight, ovarian parameters (Ovarian weight, uterine weight, the number of ovarian follicles, and corpora lutea (CL) were determined, and histopathological changes, blood profile, as well as antioxidant activity assessment, were performed. CP significantly suppresses ovarian and uterine functions and increased MAD, NO levels, RBCs, hemoglobin, WBCs, and platelet count compared to the control group ( P < 0.05). While, in CP + L-GF(equina) group, gross, histomorphometry parameters, blood, and biochemical markers were similar to that in the control. IP injection of L-GF(equina) alone significantly (P < 0.05) increased body weight, and ovarian and uterine morphometry compared with the control. CONCLUSION: co-administration of L-GF(equina) with CP might protect the reproductive organs in rats through its high antioxidant capacity.
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spelling pubmed-101419442023-04-29 Lyophilized equine platelet-rich plasma (L-GF(equina)) antagonize the Reproductive toxicity and oxidative stress Induced by Cyclophosphamide in female rats Abdoon, Ahmed Sabry S. Al-Atrash, Ahmed M.E Soliman, Seham S. El-Sanea, Amro M. Gamal el Din, Amina A. Fahmy, Hossam M. J Ovarian Res Research BACKGROUND: The antineoplastic agent Cyclophosphamide (CP) induces reproductive toxicity. New strategies for protecting ovarian tissue damage in women with chemotherapy-induced reproductive toxicity are essential. This study was designed to evaluate the possible protective effect of combined treatment with L-GF(equina) on CP-induced reproductive toxicity in the mature female rat. METHODOLOGY: Forty mature female rats were assigned into four groups: First group, control: rats were intraperitoneally injected (IP) with 200 µl sterile saline solution on days 1 and 10; Group 2 (CP): were IP injected with 75 mg/kg on days 1 and 10 to induce POI); Group 3 (CP + L-GF(equina)): as in group 2 + IP injected with 200 µl rehydrated L-GF(equina) half-hour after CP injection on day 1 and 10); Group 4 (L-GF(equina)): rats were IP injected with 200 µl L-GF(equina) on day 1 and 10). Blood samples were collected for a complete blood picture and determinations of nitric oxide and malondialdehyde. Animals were sacrificed on Day-21, and genitalia was dissected, weighed, and fixed in 10% formalin for histopathological and morphometric evaluation. RESULTS: On day 21 of the experiment, body weight, ovarian parameters (Ovarian weight, uterine weight, the number of ovarian follicles, and corpora lutea (CL) were determined, and histopathological changes, blood profile, as well as antioxidant activity assessment, were performed. CP significantly suppresses ovarian and uterine functions and increased MAD, NO levels, RBCs, hemoglobin, WBCs, and platelet count compared to the control group ( P < 0.05). While, in CP + L-GF(equina) group, gross, histomorphometry parameters, blood, and biochemical markers were similar to that in the control. IP injection of L-GF(equina) alone significantly (P < 0.05) increased body weight, and ovarian and uterine morphometry compared with the control. CONCLUSION: co-administration of L-GF(equina) with CP might protect the reproductive organs in rats through its high antioxidant capacity. BioMed Central 2023-04-28 /pmc/articles/PMC10141944/ /pubmed/37118826 http://dx.doi.org/10.1186/s13048-023-01161-x Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Abdoon, Ahmed Sabry S.
Al-Atrash, Ahmed M.E
Soliman, Seham S.
El-Sanea, Amro M.
Gamal el Din, Amina A.
Fahmy, Hossam M.
Lyophilized equine platelet-rich plasma (L-GF(equina)) antagonize the Reproductive toxicity and oxidative stress Induced by Cyclophosphamide in female rats
title Lyophilized equine platelet-rich plasma (L-GF(equina)) antagonize the Reproductive toxicity and oxidative stress Induced by Cyclophosphamide in female rats
title_full Lyophilized equine platelet-rich plasma (L-GF(equina)) antagonize the Reproductive toxicity and oxidative stress Induced by Cyclophosphamide in female rats
title_fullStr Lyophilized equine platelet-rich plasma (L-GF(equina)) antagonize the Reproductive toxicity and oxidative stress Induced by Cyclophosphamide in female rats
title_full_unstemmed Lyophilized equine platelet-rich plasma (L-GF(equina)) antagonize the Reproductive toxicity and oxidative stress Induced by Cyclophosphamide in female rats
title_short Lyophilized equine platelet-rich plasma (L-GF(equina)) antagonize the Reproductive toxicity and oxidative stress Induced by Cyclophosphamide in female rats
title_sort lyophilized equine platelet-rich plasma (l-gf(equina)) antagonize the reproductive toxicity and oxidative stress induced by cyclophosphamide in female rats
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10141944/
https://www.ncbi.nlm.nih.gov/pubmed/37118826
http://dx.doi.org/10.1186/s13048-023-01161-x
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