Cargando…

Supplementation of Abelmoschus manihot Ameliorates Diabetic Nephropathy and Hepatic Steatosis by Activating Autophagy in Mice

Diabetic nephropathy (DN) is a diabetic complication marked by albuminuria and a decline of the glomerular filtration rate. Diabetic kidneys are defective in the autophagy process and mitochondrial function and their enhancement of activity alleviates the pathology. In this paper, we developed a mou...

Descripción completa

Detalles Bibliográficos
Autores principales: Kim, Hwajin, Dusabimana, Theodomir, Kim, So Ra, Je, Jihyun, Jeong, Kyuho, Kang, Min Cheol, Cho, Kye Man, Kim, Hye Jung, Park, Sang Won
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6266484/
https://www.ncbi.nlm.nih.gov/pubmed/30405076
http://dx.doi.org/10.3390/nu10111703
_version_ 1783375849704128512
author Kim, Hwajin
Dusabimana, Theodomir
Kim, So Ra
Je, Jihyun
Jeong, Kyuho
Kang, Min Cheol
Cho, Kye Man
Kim, Hye Jung
Park, Sang Won
author_facet Kim, Hwajin
Dusabimana, Theodomir
Kim, So Ra
Je, Jihyun
Jeong, Kyuho
Kang, Min Cheol
Cho, Kye Man
Kim, Hye Jung
Park, Sang Won
author_sort Kim, Hwajin
collection PubMed
description Diabetic nephropathy (DN) is a diabetic complication marked by albuminuria and a decline of the glomerular filtration rate. Diabetic kidneys are defective in the autophagy process and mitochondrial function and their enhancement of activity alleviates the pathology. In this paper, we developed a mouse model of DN by a combined treatment of a high-fat diet and streptozotocin after unilateral nephrectomy and supplementation with flower or leaf extracts of Abelmoschus manihot (AM) were tested. The preventive effects of the extracts on DN pathology and changes on autophagy and mitochondrial proteins were investigated. DN mice showed a significant increase in fasting blood glucose, plasma creatinine, blood urea nitrogen, and urinary albumin levels. Periodic acid–Schiff and Sirius red staining of the diabetic kidney presented a significant change in glomerular and tubular structures that was associated with podocyte loss and fibrotic protein accumulation. These changes were attenuated by AM extract treatment in DN mice. In addition, hepatic injury, proinflammatory cytokines, and lipid accumulation were decreased by AM extracts in DN mice. As a protective mechanism, AM extracts significantly increased the expression of proteins by regulating autophagy and mitochondrial dynamics, which potentially prevented the kidney and liver from accumulating pathogenic proteins and dysfunctional mitochondria, which alleviated the progression of DN.
format Online
Article
Text
id pubmed-6266484
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-62664842018-12-06 Supplementation of Abelmoschus manihot Ameliorates Diabetic Nephropathy and Hepatic Steatosis by Activating Autophagy in Mice Kim, Hwajin Dusabimana, Theodomir Kim, So Ra Je, Jihyun Jeong, Kyuho Kang, Min Cheol Cho, Kye Man Kim, Hye Jung Park, Sang Won Nutrients Article Diabetic nephropathy (DN) is a diabetic complication marked by albuminuria and a decline of the glomerular filtration rate. Diabetic kidneys are defective in the autophagy process and mitochondrial function and their enhancement of activity alleviates the pathology. In this paper, we developed a mouse model of DN by a combined treatment of a high-fat diet and streptozotocin after unilateral nephrectomy and supplementation with flower or leaf extracts of Abelmoschus manihot (AM) were tested. The preventive effects of the extracts on DN pathology and changes on autophagy and mitochondrial proteins were investigated. DN mice showed a significant increase in fasting blood glucose, plasma creatinine, blood urea nitrogen, and urinary albumin levels. Periodic acid–Schiff and Sirius red staining of the diabetic kidney presented a significant change in glomerular and tubular structures that was associated with podocyte loss and fibrotic protein accumulation. These changes were attenuated by AM extract treatment in DN mice. In addition, hepatic injury, proinflammatory cytokines, and lipid accumulation were decreased by AM extracts in DN mice. As a protective mechanism, AM extracts significantly increased the expression of proteins by regulating autophagy and mitochondrial dynamics, which potentially prevented the kidney and liver from accumulating pathogenic proteins and dysfunctional mitochondria, which alleviated the progression of DN. MDPI 2018-11-07 /pmc/articles/PMC6266484/ /pubmed/30405076 http://dx.doi.org/10.3390/nu10111703 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Kim, Hwajin
Dusabimana, Theodomir
Kim, So Ra
Je, Jihyun
Jeong, Kyuho
Kang, Min Cheol
Cho, Kye Man
Kim, Hye Jung
Park, Sang Won
Supplementation of Abelmoschus manihot Ameliorates Diabetic Nephropathy and Hepatic Steatosis by Activating Autophagy in Mice
title Supplementation of Abelmoschus manihot Ameliorates Diabetic Nephropathy and Hepatic Steatosis by Activating Autophagy in Mice
title_full Supplementation of Abelmoschus manihot Ameliorates Diabetic Nephropathy and Hepatic Steatosis by Activating Autophagy in Mice
title_fullStr Supplementation of Abelmoschus manihot Ameliorates Diabetic Nephropathy and Hepatic Steatosis by Activating Autophagy in Mice
title_full_unstemmed Supplementation of Abelmoschus manihot Ameliorates Diabetic Nephropathy and Hepatic Steatosis by Activating Autophagy in Mice
title_short Supplementation of Abelmoschus manihot Ameliorates Diabetic Nephropathy and Hepatic Steatosis by Activating Autophagy in Mice
title_sort supplementation of abelmoschus manihot ameliorates diabetic nephropathy and hepatic steatosis by activating autophagy in mice
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6266484/
https://www.ncbi.nlm.nih.gov/pubmed/30405076
http://dx.doi.org/10.3390/nu10111703
work_keys_str_mv AT kimhwajin supplementationofabelmoschusmanihotamelioratesdiabeticnephropathyandhepaticsteatosisbyactivatingautophagyinmice
AT dusabimanatheodomir supplementationofabelmoschusmanihotamelioratesdiabeticnephropathyandhepaticsteatosisbyactivatingautophagyinmice
AT kimsora supplementationofabelmoschusmanihotamelioratesdiabeticnephropathyandhepaticsteatosisbyactivatingautophagyinmice
AT jejihyun supplementationofabelmoschusmanihotamelioratesdiabeticnephropathyandhepaticsteatosisbyactivatingautophagyinmice
AT jeongkyuho supplementationofabelmoschusmanihotamelioratesdiabeticnephropathyandhepaticsteatosisbyactivatingautophagyinmice
AT kangmincheol supplementationofabelmoschusmanihotamelioratesdiabeticnephropathyandhepaticsteatosisbyactivatingautophagyinmice
AT chokyeman supplementationofabelmoschusmanihotamelioratesdiabeticnephropathyandhepaticsteatosisbyactivatingautophagyinmice
AT kimhyejung supplementationofabelmoschusmanihotamelioratesdiabeticnephropathyandhepaticsteatosisbyactivatingautophagyinmice
AT parksangwon supplementationofabelmoschusmanihotamelioratesdiabeticnephropathyandhepaticsteatosisbyactivatingautophagyinmice