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Effectiveness of forest honey ( Apis dorsata) as therapy for ovarian failure causing malnutrition

Background: Malnutrition is the imbalance between intake and nutritional needs, resulting in a decrease in body weight, composition, and physical function. Malnutrition causes infertility due to intestinal and liver degeneration,which may progress to testicular and ovarian degeneration. Methods: An...

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Autores principales: Safitri, Erma, Purnobasuki, Hery, Purnama, Muhammad Thohawi Elziyad, Chhetri, Shekhar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: F1000 Research Limited 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521050/
https://www.ncbi.nlm.nih.gov/pubmed/37767071
http://dx.doi.org/10.12688/f1000research.110660.2
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author Safitri, Erma
Purnobasuki, Hery
Purnama, Muhammad Thohawi Elziyad
Chhetri, Shekhar
author_facet Safitri, Erma
Purnobasuki, Hery
Purnama, Muhammad Thohawi Elziyad
Chhetri, Shekhar
author_sort Safitri, Erma
collection PubMed
description Background: Malnutrition is the imbalance between intake and nutritional needs, resulting in a decrease in body weight, composition, and physical function. Malnutrition causes infertility due to intestinal and liver degeneration,which may progress to testicular and ovarian degeneration. Methods: An infertile female rat model with a degenerative ovary was induced with malnutrition through a 5-day food fasting but still had drinking water. The administration of (T1) 30% (v/v) and (T2) 50% (v/v) forest honey ( Apis dorsata) were performed for ten consecutive days, whereas the (T+) group was fasted and not administered forest honey and the (T−) group has not fasted and not administered forest honey. Superoxide dismutase, malondialdehyde, IL-13 and TNF-α cytokine expressions, and ovarian tissue regeneration were analyzed. Results: Superoxide dismutase was significantly different ( p<0.05) in T1 (65.24±7.53), T2 (74.16±12.3), and T− (65.09±6.56) compared with T+ (41.76±8.51). Malondialdehyde was significantly different ( p<0.05) in T1 (9.71±1.53), T2 (9.23±0.96), and T− (9.83±1.46) compared with T+ (15.28±1.61). Anti-inflammatory cytokine (IL-13) expression was significantly different ( p<0.05) in T1 (5.30±2.31), T2 (9.80±2.53), and T− (0.30±0.48) compared with T+ (2.70±1.57). Pro-inflammatory cytokine (TNF-α) expression was significantly different ( p<0.05) in T1 (4.40±3.02), T2 (2.50±1.65), and T− (0.30±0.48) compared with T+ (9.50±1.78). Ovarian tissue regeneration was significantly different ( p<0.05) in T− (8.6±0.69) and T2 (5.10±0.99) compared with T1 (0.7±0.95) and T+ (0.3±0.67). Conclusion: The 10-day administration of 50% (v/v) forest honey can be an effective therapy for ovarian failure that caused malnutrition in the female rat model.
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spelling pubmed-105210502023-09-27 Effectiveness of forest honey ( Apis dorsata) as therapy for ovarian failure causing malnutrition Safitri, Erma Purnobasuki, Hery Purnama, Muhammad Thohawi Elziyad Chhetri, Shekhar F1000Res Research Article Background: Malnutrition is the imbalance between intake and nutritional needs, resulting in a decrease in body weight, composition, and physical function. Malnutrition causes infertility due to intestinal and liver degeneration,which may progress to testicular and ovarian degeneration. Methods: An infertile female rat model with a degenerative ovary was induced with malnutrition through a 5-day food fasting but still had drinking water. The administration of (T1) 30% (v/v) and (T2) 50% (v/v) forest honey ( Apis dorsata) were performed for ten consecutive days, whereas the (T+) group was fasted and not administered forest honey and the (T−) group has not fasted and not administered forest honey. Superoxide dismutase, malondialdehyde, IL-13 and TNF-α cytokine expressions, and ovarian tissue regeneration were analyzed. Results: Superoxide dismutase was significantly different ( p<0.05) in T1 (65.24±7.53), T2 (74.16±12.3), and T− (65.09±6.56) compared with T+ (41.76±8.51). Malondialdehyde was significantly different ( p<0.05) in T1 (9.71±1.53), T2 (9.23±0.96), and T− (9.83±1.46) compared with T+ (15.28±1.61). Anti-inflammatory cytokine (IL-13) expression was significantly different ( p<0.05) in T1 (5.30±2.31), T2 (9.80±2.53), and T− (0.30±0.48) compared with T+ (2.70±1.57). Pro-inflammatory cytokine (TNF-α) expression was significantly different ( p<0.05) in T1 (4.40±3.02), T2 (2.50±1.65), and T− (0.30±0.48) compared with T+ (9.50±1.78). Ovarian tissue regeneration was significantly different ( p<0.05) in T− (8.6±0.69) and T2 (5.10±0.99) compared with T1 (0.7±0.95) and T+ (0.3±0.67). Conclusion: The 10-day administration of 50% (v/v) forest honey can be an effective therapy for ovarian failure that caused malnutrition in the female rat model. F1000 Research Limited 2022-10-20 /pmc/articles/PMC10521050/ /pubmed/37767071 http://dx.doi.org/10.12688/f1000research.110660.2 Text en Copyright: © 2022 Safitri E et al. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Safitri, Erma
Purnobasuki, Hery
Purnama, Muhammad Thohawi Elziyad
Chhetri, Shekhar
Effectiveness of forest honey ( Apis dorsata) as therapy for ovarian failure causing malnutrition
title Effectiveness of forest honey ( Apis dorsata) as therapy for ovarian failure causing malnutrition
title_full Effectiveness of forest honey ( Apis dorsata) as therapy for ovarian failure causing malnutrition
title_fullStr Effectiveness of forest honey ( Apis dorsata) as therapy for ovarian failure causing malnutrition
title_full_unstemmed Effectiveness of forest honey ( Apis dorsata) as therapy for ovarian failure causing malnutrition
title_short Effectiveness of forest honey ( Apis dorsata) as therapy for ovarian failure causing malnutrition
title_sort effectiveness of forest honey ( apis dorsata) as therapy for ovarian failure causing malnutrition
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10521050/
https://www.ncbi.nlm.nih.gov/pubmed/37767071
http://dx.doi.org/10.12688/f1000research.110660.2
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