Cargando…

Impact of diabetes on male sexual function in streptozotocin-induced diabetic rats: Protective role of soluble epoxide hydrolase inhibitor

Diabetes-induced male sexual dysfunction is associated with endothelial dysfunction. Inhibition of soluble epoxide hydrolase (sEH) is known to improve endothelial function in diabetes. Therefore, we hypothesized that sEH inhibitor (sEHI), [trans-4-{4-[3-(4-trifluoromethoxyphenyl)-ureido]cyclohexylox...

Descripción completa

Detalles Bibliográficos
Autores principales: Minaz, Nathani, Razdan, Rema, Hammock, Bruce D., Mujwar, Somdutt, Goswami, Sumanta Kumar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893866/
https://www.ncbi.nlm.nih.gov/pubmed/31102913
http://dx.doi.org/10.1016/j.biopha.2019.108897
_version_ 1783476295017955328
author Minaz, Nathani
Razdan, Rema
Hammock, Bruce D.
Mujwar, Somdutt
Goswami, Sumanta Kumar
author_facet Minaz, Nathani
Razdan, Rema
Hammock, Bruce D.
Mujwar, Somdutt
Goswami, Sumanta Kumar
author_sort Minaz, Nathani
collection PubMed
description Diabetes-induced male sexual dysfunction is associated with endothelial dysfunction. Inhibition of soluble epoxide hydrolase (sEH) is known to improve endothelial function in diabetes. Therefore, we hypothesized that sEH inhibitor (sEHI), [trans-4-{4-[3-(4-trifluoromethoxyphenyl)-ureido]cyclohexyloxy}benzoic acid] / t-TUCB can restore the male sexual function in diabetic rat. After one week of administration of diabetogenic agent STZ (52 mg/kg i.p) injection, diabetic rats were treated with t-TUCB (0.1 and 0.3 mg/kg, p.o) or vehicle for 8 weeks. The sexual behaviour parameters of the animals were evaluated at the end of dosing period. The levels of testosterone and glucose in serum, and sperm were quantified. Effect of treatment on weight of reproductive organs and histopathology of penile tissue was evaluated. Diabetes had a negative effect on male sexual function, weight of sexual organs and production of sperm with a parallel decrease in the level of testosterone. The sEHI, t-TUCB, significantly preserved the sexual function and minimized an increase in the level of blood glucose in diabetic rats. It also prevented a decrease in the level of testosterone and sperm in diabetic rats, in comparison to diabetic control rats. Further, diabetes induced distortion of corpus cavernosum was attenuated by t-TUCB. Based on our findings, sEHI may delay the development of sexual dysfunction in diabetes.
format Online
Article
Text
id pubmed-6893866
institution National Center for Biotechnology Information
language English
publishDate 2019
record_format MEDLINE/PubMed
spelling pubmed-68938662020-07-01 Impact of diabetes on male sexual function in streptozotocin-induced diabetic rats: Protective role of soluble epoxide hydrolase inhibitor Minaz, Nathani Razdan, Rema Hammock, Bruce D. Mujwar, Somdutt Goswami, Sumanta Kumar Biomed Pharmacother Article Diabetes-induced male sexual dysfunction is associated with endothelial dysfunction. Inhibition of soluble epoxide hydrolase (sEH) is known to improve endothelial function in diabetes. Therefore, we hypothesized that sEH inhibitor (sEHI), [trans-4-{4-[3-(4-trifluoromethoxyphenyl)-ureido]cyclohexyloxy}benzoic acid] / t-TUCB can restore the male sexual function in diabetic rat. After one week of administration of diabetogenic agent STZ (52 mg/kg i.p) injection, diabetic rats were treated with t-TUCB (0.1 and 0.3 mg/kg, p.o) or vehicle for 8 weeks. The sexual behaviour parameters of the animals were evaluated at the end of dosing period. The levels of testosterone and glucose in serum, and sperm were quantified. Effect of treatment on weight of reproductive organs and histopathology of penile tissue was evaluated. Diabetes had a negative effect on male sexual function, weight of sexual organs and production of sperm with a parallel decrease in the level of testosterone. The sEHI, t-TUCB, significantly preserved the sexual function and minimized an increase in the level of blood glucose in diabetic rats. It also prevented a decrease in the level of testosterone and sperm in diabetic rats, in comparison to diabetic control rats. Further, diabetes induced distortion of corpus cavernosum was attenuated by t-TUCB. Based on our findings, sEHI may delay the development of sexual dysfunction in diabetes. 2019-05-15 2019-07 /pmc/articles/PMC6893866/ /pubmed/31102913 http://dx.doi.org/10.1016/j.biopha.2019.108897 Text en https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/BY/4.0/ (https://creativecommons.org/licenses/by/4.0/) ).
spellingShingle Article
Minaz, Nathani
Razdan, Rema
Hammock, Bruce D.
Mujwar, Somdutt
Goswami, Sumanta Kumar
Impact of diabetes on male sexual function in streptozotocin-induced diabetic rats: Protective role of soluble epoxide hydrolase inhibitor
title Impact of diabetes on male sexual function in streptozotocin-induced diabetic rats: Protective role of soluble epoxide hydrolase inhibitor
title_full Impact of diabetes on male sexual function in streptozotocin-induced diabetic rats: Protective role of soluble epoxide hydrolase inhibitor
title_fullStr Impact of diabetes on male sexual function in streptozotocin-induced diabetic rats: Protective role of soluble epoxide hydrolase inhibitor
title_full_unstemmed Impact of diabetes on male sexual function in streptozotocin-induced diabetic rats: Protective role of soluble epoxide hydrolase inhibitor
title_short Impact of diabetes on male sexual function in streptozotocin-induced diabetic rats: Protective role of soluble epoxide hydrolase inhibitor
title_sort impact of diabetes on male sexual function in streptozotocin-induced diabetic rats: protective role of soluble epoxide hydrolase inhibitor
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6893866/
https://www.ncbi.nlm.nih.gov/pubmed/31102913
http://dx.doi.org/10.1016/j.biopha.2019.108897
work_keys_str_mv AT minaznathani impactofdiabetesonmalesexualfunctioninstreptozotocininduceddiabeticratsprotectiveroleofsolubleepoxidehydrolaseinhibitor
AT razdanrema impactofdiabetesonmalesexualfunctioninstreptozotocininduceddiabeticratsprotectiveroleofsolubleepoxidehydrolaseinhibitor
AT hammockbruced impactofdiabetesonmalesexualfunctioninstreptozotocininduceddiabeticratsprotectiveroleofsolubleepoxidehydrolaseinhibitor
AT mujwarsomdutt impactofdiabetesonmalesexualfunctioninstreptozotocininduceddiabeticratsprotectiveroleofsolubleepoxidehydrolaseinhibitor
AT goswamisumantakumar impactofdiabetesonmalesexualfunctioninstreptozotocininduceddiabeticratsprotectiveroleofsolubleepoxidehydrolaseinhibitor