Mucuna pruriens restores spermatogenesis in mice after exposure to 2-methoxyethanol

Background Increasing industrial activity is causing many problems in reproductive health, such as infertility. The factors causing infertility are hormones, infection, radiation, drugs and chemicals. One of these is 2-methoxyethanol (2-ME). The objective of this study was to evaluate the effect o...

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Main Authors: Putu Oky Ari Tania, Sri Winarni
Format: Article
Language:English
Published: Faculty of Medicine Trisakti University 2013-12-01
Series:Universa Medicina
Subjects:
Online Access:http://www.univmed.org/wp-content/uploads/2014/01/putu1.pdf
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author Putu Oky Ari Tania
Sri Winarni
author_facet Putu Oky Ari Tania
Sri Winarni
author_sort Putu Oky Ari Tania
collection DOAJ
description Background Increasing industrial activity is causing many problems in reproductive health, such as infertility. The factors causing infertility are hormones, infection, radiation, drugs and chemicals. One of these is 2-methoxyethanol (2-ME). The objective of this study was to evaluate the effect of Mucuna pruriens (MP) seed fraction on spermatogenesis, including number of spermatogenic cells and spermatozoal membrane protein profiles after exposure to 2-ME in mice. Methods This study was of experimental design. Thirty mice were randomized into 5 groups, i.e. 2 control groups and 3 treatment groups. All mice were injected subcutaneously with 2-ME doses of 100mg/kg body weight (BW)/day, for a period of 12 days. Positive (PC) and negative controls (NC) were treated with carboxy methyl cellulose (CMC). The three treatment groups were given MP seed fraction in doses of 14 (T1), 28 (T2) and 56 mg/kg BW (T3), respectively, from day 13 until day 64. Data on spermatogenic cells were collected from histological cross-sections and analyzed with one-way ANOVA. The spermatozoal membrane protein profile was identified by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) with silver staining and were analyzed descriptively. Results Administration of MP seed fractions resulted in significantly different numbers of spermatocytes I and round spermatids between PC and T1, T2, and T3. A protein with the molecular weight of 41.6 kDa was expressed in all groups except the positive controls, while a 24.5 kDa protein was expressed in the positive controls only. Conclusion MP seed fraction effectively recovers spermatogenesis loss in mice due to 2-ME exposure.
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spelling doaj.art-5858758b7fa04870b95b0360e38b066b2022-12-21T19:40:09ZengFaculty of Medicine Trisakti UniversityUniversa Medicina1907-30622013-12-01323137145Mucuna pruriens restores spermatogenesis in mice after exposure to 2-methoxyethanolPutu Oky Ari Tania0Sri Winarni1Biomedical Department and Medical Genetics Laboratory, Biomolecular Research Center, Faculty of Medicine, Wijaya Kusuma University, Surabaya Department of Public Health, Faculty of Medicine, Diponogoro UniversityBackground Increasing industrial activity is causing many problems in reproductive health, such as infertility. The factors causing infertility are hormones, infection, radiation, drugs and chemicals. One of these is 2-methoxyethanol (2-ME). The objective of this study was to evaluate the effect of Mucuna pruriens (MP) seed fraction on spermatogenesis, including number of spermatogenic cells and spermatozoal membrane protein profiles after exposure to 2-ME in mice. Methods This study was of experimental design. Thirty mice were randomized into 5 groups, i.e. 2 control groups and 3 treatment groups. All mice were injected subcutaneously with 2-ME doses of 100mg/kg body weight (BW)/day, for a period of 12 days. Positive (PC) and negative controls (NC) were treated with carboxy methyl cellulose (CMC). The three treatment groups were given MP seed fraction in doses of 14 (T1), 28 (T2) and 56 mg/kg BW (T3), respectively, from day 13 until day 64. Data on spermatogenic cells were collected from histological cross-sections and analyzed with one-way ANOVA. The spermatozoal membrane protein profile was identified by sodium dodecyl sulfate polyacrylamide gel electrophoresis (SDS-PAGE) with silver staining and were analyzed descriptively. Results Administration of MP seed fractions resulted in significantly different numbers of spermatocytes I and round spermatids between PC and T1, T2, and T3. A protein with the molecular weight of 41.6 kDa was expressed in all groups except the positive controls, while a 24.5 kDa protein was expressed in the positive controls only. Conclusion MP seed fraction effectively recovers spermatogenesis loss in mice due to 2-ME exposure.http://www.univmed.org/wp-content/uploads/2014/01/putu1.pdfMucuna pruriens2-methoxyethanolspermatogenic cellsmice
spellingShingle Putu Oky Ari Tania
Sri Winarni
Mucuna pruriens restores spermatogenesis in mice after exposure to 2-methoxyethanol
Universa Medicina
Mucuna pruriens
2-methoxyethanol
spermatogenic cells
mice
title Mucuna pruriens restores spermatogenesis in mice after exposure to 2-methoxyethanol
title_full Mucuna pruriens restores spermatogenesis in mice after exposure to 2-methoxyethanol
title_fullStr Mucuna pruriens restores spermatogenesis in mice after exposure to 2-methoxyethanol
title_full_unstemmed Mucuna pruriens restores spermatogenesis in mice after exposure to 2-methoxyethanol
title_short Mucuna pruriens restores spermatogenesis in mice after exposure to 2-methoxyethanol
title_sort mucuna pruriens restores spermatogenesis in mice after exposure to 2 methoxyethanol
topic Mucuna pruriens
2-methoxyethanol
spermatogenic cells
mice
url http://www.univmed.org/wp-content/uploads/2014/01/putu1.pdf
work_keys_str_mv AT putuokyaritania mucunapruriensrestoresspermatogenesisinmiceafterexposureto2methoxyethanol
AT sriwinarni mucunapruriensrestoresspermatogenesisinmiceafterexposureto2methoxyethanol