Cargando…

Reno-Hepatoprotective and Antidiabetic Properties of Methanol Leaf Extract of Laportea Aestuans in Wistar Rats

Toxicities due to exposure to arsenic-contaminated water and the occurrence of diabetes mellitus are major health concerns. Treatment of these concerns using therapeutic measures have recorded limited success. Traditionally, Laportea aestuans (LA) has been used in managing various diseases. Hence, w...

Descripción completa

Detalles Bibliográficos
Autores principales: Adetunji, Oluwaseyi Adegoke, Olugbami, Jeremiah Olorunjuwon, Adegoke, Ayodeji Mathias, Gbadegesin, Michael Adedapo, Odunola, Oyeronke Adunni
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168169/
https://www.ncbi.nlm.nih.gov/pubmed/34039071
http://dx.doi.org/10.1177/2515690X211017464
_version_ 1783701834737647616
author Adetunji, Oluwaseyi Adegoke
Olugbami, Jeremiah Olorunjuwon
Adegoke, Ayodeji Mathias
Gbadegesin, Michael Adedapo
Odunola, Oyeronke Adunni
author_facet Adetunji, Oluwaseyi Adegoke
Olugbami, Jeremiah Olorunjuwon
Adegoke, Ayodeji Mathias
Gbadegesin, Michael Adedapo
Odunola, Oyeronke Adunni
author_sort Adetunji, Oluwaseyi Adegoke
collection PubMed
description Toxicities due to exposure to arsenic-contaminated water and the occurrence of diabetes mellitus are major health concerns. Treatment of these concerns using therapeutic measures have recorded limited success. Traditionally, Laportea aestuans (LA) has been used in managing various diseases. Hence, we investigated the reno-hepatoprotective/antidiabetic potentials of methanol leaf extract of LA (MeLELA) in male Wistar rats. Thirty rats (100-150 g) were equally distributed into 6 groups: Group I (vehicle-treated); group II received 2.5 mg/kg sodium arsenite (SA) thrice a week for 2 weeks; group III received streptozotocin (STZ, 50 mg/kg once); group IV received 200 mg/kg LA daily for 14 days; group V received SA and LA; group VI received STZ and LA. Sodium arsenite and STZ induced reno-hepatotoxicity and diabetes, respectively. Phytochemical screening, biomarkers/enzyme activities, blood glucose levels, micronucleus assay, kidney, liver and pancreas histologies were determined according to standard procedures. Alkaloids, carotenoids and flavonoids were present in abundance. Both SA-and STZ-treated groups recorded significant (p < 0.05) reductions in serum protein concentrations, while co-treatment with LA significantly restored the levels. The SA-induced significant increase in creatinine/urea levels were significantly reduced by LA. Co-treatment of each of SA-and STZ-treated groups, respectively, with LA significantly decreased the elevated serum alanine and aspartate aminotransferases’ activities. Increased blood glucose level in diabetic group was remarkably lowered by LA. Also, the SA-induced frequency of micronucleated polychromatic erythrocytes was significantly ameliorated by LA. Conclusively, LA is protective against SA-induced toxicity and STZ-induced diabetes in Wistar rats.
format Online
Article
Text
id pubmed-8168169
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher SAGE Publications
record_format MEDLINE/PubMed
spelling pubmed-81681692021-06-07 Reno-Hepatoprotective and Antidiabetic Properties of Methanol Leaf Extract of Laportea Aestuans in Wistar Rats Adetunji, Oluwaseyi Adegoke Olugbami, Jeremiah Olorunjuwon Adegoke, Ayodeji Mathias Gbadegesin, Michael Adedapo Odunola, Oyeronke Adunni J Evid Based Integr Med Original Manuscript Toxicities due to exposure to arsenic-contaminated water and the occurrence of diabetes mellitus are major health concerns. Treatment of these concerns using therapeutic measures have recorded limited success. Traditionally, Laportea aestuans (LA) has been used in managing various diseases. Hence, we investigated the reno-hepatoprotective/antidiabetic potentials of methanol leaf extract of LA (MeLELA) in male Wistar rats. Thirty rats (100-150 g) were equally distributed into 6 groups: Group I (vehicle-treated); group II received 2.5 mg/kg sodium arsenite (SA) thrice a week for 2 weeks; group III received streptozotocin (STZ, 50 mg/kg once); group IV received 200 mg/kg LA daily for 14 days; group V received SA and LA; group VI received STZ and LA. Sodium arsenite and STZ induced reno-hepatotoxicity and diabetes, respectively. Phytochemical screening, biomarkers/enzyme activities, blood glucose levels, micronucleus assay, kidney, liver and pancreas histologies were determined according to standard procedures. Alkaloids, carotenoids and flavonoids were present in abundance. Both SA-and STZ-treated groups recorded significant (p < 0.05) reductions in serum protein concentrations, while co-treatment with LA significantly restored the levels. The SA-induced significant increase in creatinine/urea levels were significantly reduced by LA. Co-treatment of each of SA-and STZ-treated groups, respectively, with LA significantly decreased the elevated serum alanine and aspartate aminotransferases’ activities. Increased blood glucose level in diabetic group was remarkably lowered by LA. Also, the SA-induced frequency of micronucleated polychromatic erythrocytes was significantly ameliorated by LA. Conclusively, LA is protective against SA-induced toxicity and STZ-induced diabetes in Wistar rats. SAGE Publications 2021-05-26 /pmc/articles/PMC8168169/ /pubmed/34039071 http://dx.doi.org/10.1177/2515690X211017464 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Manuscript
Adetunji, Oluwaseyi Adegoke
Olugbami, Jeremiah Olorunjuwon
Adegoke, Ayodeji Mathias
Gbadegesin, Michael Adedapo
Odunola, Oyeronke Adunni
Reno-Hepatoprotective and Antidiabetic Properties of Methanol Leaf Extract of Laportea Aestuans in Wistar Rats
title Reno-Hepatoprotective and Antidiabetic Properties of Methanol Leaf Extract of Laportea Aestuans in Wistar Rats
title_full Reno-Hepatoprotective and Antidiabetic Properties of Methanol Leaf Extract of Laportea Aestuans in Wistar Rats
title_fullStr Reno-Hepatoprotective and Antidiabetic Properties of Methanol Leaf Extract of Laportea Aestuans in Wistar Rats
title_full_unstemmed Reno-Hepatoprotective and Antidiabetic Properties of Methanol Leaf Extract of Laportea Aestuans in Wistar Rats
title_short Reno-Hepatoprotective and Antidiabetic Properties of Methanol Leaf Extract of Laportea Aestuans in Wistar Rats
title_sort reno-hepatoprotective and antidiabetic properties of methanol leaf extract of laportea aestuans in wistar rats
topic Original Manuscript
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8168169/
https://www.ncbi.nlm.nih.gov/pubmed/34039071
http://dx.doi.org/10.1177/2515690X211017464
work_keys_str_mv AT adetunjioluwaseyiadegoke renohepatoprotectiveandantidiabeticpropertiesofmethanolleafextractoflaporteaaestuansinwistarrats
AT olugbamijeremiaholorunjuwon renohepatoprotectiveandantidiabeticpropertiesofmethanolleafextractoflaporteaaestuansinwistarrats
AT adegokeayodejimathias renohepatoprotectiveandantidiabeticpropertiesofmethanolleafextractoflaporteaaestuansinwistarrats
AT gbadegesinmichaeladedapo renohepatoprotectiveandantidiabeticpropertiesofmethanolleafextractoflaporteaaestuansinwistarrats
AT odunolaoyeronkeadunni renohepatoprotectiveandantidiabeticpropertiesofmethanolleafextractoflaporteaaestuansinwistarrats