Cargando…

Neuroprotective Effect of Red Sea Marine Sponge Xestospongia testudinaria Extract Using In Vitro and In Vivo Diabetic Peripheral Neuropathy Models

Diabetic peripheral neuropathy (DPN) is a common complication of diabetes. Oxidative stress plays an important role in the pathophysiology of DPN. Red Sea marine sponge Xestospongia testudinaria extract has a promising neuroprotective effect, presumably owing to its antioxidant and anti-inflammatory...

Descripción completa

Detalles Bibliográficos
Autores principales: Magadmi, Rania, Borouk, Kariman, Youssef, Diaa T. A., Shaala, Lamiaa A., Alrafiah, Aziza R., Shaik, Rasheed A., Alharthi, Sameer E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9693000/
https://www.ncbi.nlm.nih.gov/pubmed/36355482
http://dx.doi.org/10.3390/ph15111309
_version_ 1784837419507384320
author Magadmi, Rania
Borouk, Kariman
Youssef, Diaa T. A.
Shaala, Lamiaa A.
Alrafiah, Aziza R.
Shaik, Rasheed A.
Alharthi, Sameer E.
author_facet Magadmi, Rania
Borouk, Kariman
Youssef, Diaa T. A.
Shaala, Lamiaa A.
Alrafiah, Aziza R.
Shaik, Rasheed A.
Alharthi, Sameer E.
author_sort Magadmi, Rania
collection PubMed
description Diabetic peripheral neuropathy (DPN) is a common complication of diabetes. Oxidative stress plays an important role in the pathophysiology of DPN. Red Sea marine sponge Xestospongia testudinaria extract has a promising neuroprotective effect, presumably owing to its antioxidant and anti-inflammatory properties. Thus, this study aimed to investigate the neuroprotective effect of the sponge X. testudinaria extract on in vitro and in vivo models of DPN. Mice dorsal root ganglia (DRG) were cultured with high glucose (HG) media and used as an in vitro model of DPN. Some of the DRGs were pre-treated with 2 mg/mL of X. testudinaria. The X. testudinaria extract significantly improved the HG-induced decreased neuronal viability and the neurite length. It improved the oxidative stress biomarkers in DRG cultures. The DPN model was induced in vivo by an injection of streptozotocin at a dose of 150 mg/kg in mice. After 35 days, 0.75 mg/kg of the X. testudinaria extract improved the hot hyperalgesia and the DRG histology. Although the sponge extract did not reduce hyperglycemia, it ameliorated the oxidative stress markers and pro-inflammatory markers in the DRG. In conclusion, the current study demonstrates the neuroprotective effect of Red Sea sponge X. testudinaria extract against experimentally induced DPN through its antioxidant and anti-inflammatory mechanisms.
format Online
Article
Text
id pubmed-9693000
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher MDPI
record_format MEDLINE/PubMed
spelling pubmed-96930002022-11-26 Neuroprotective Effect of Red Sea Marine Sponge Xestospongia testudinaria Extract Using In Vitro and In Vivo Diabetic Peripheral Neuropathy Models Magadmi, Rania Borouk, Kariman Youssef, Diaa T. A. Shaala, Lamiaa A. Alrafiah, Aziza R. Shaik, Rasheed A. Alharthi, Sameer E. Pharmaceuticals (Basel) Article Diabetic peripheral neuropathy (DPN) is a common complication of diabetes. Oxidative stress plays an important role in the pathophysiology of DPN. Red Sea marine sponge Xestospongia testudinaria extract has a promising neuroprotective effect, presumably owing to its antioxidant and anti-inflammatory properties. Thus, this study aimed to investigate the neuroprotective effect of the sponge X. testudinaria extract on in vitro and in vivo models of DPN. Mice dorsal root ganglia (DRG) were cultured with high glucose (HG) media and used as an in vitro model of DPN. Some of the DRGs were pre-treated with 2 mg/mL of X. testudinaria. The X. testudinaria extract significantly improved the HG-induced decreased neuronal viability and the neurite length. It improved the oxidative stress biomarkers in DRG cultures. The DPN model was induced in vivo by an injection of streptozotocin at a dose of 150 mg/kg in mice. After 35 days, 0.75 mg/kg of the X. testudinaria extract improved the hot hyperalgesia and the DRG histology. Although the sponge extract did not reduce hyperglycemia, it ameliorated the oxidative stress markers and pro-inflammatory markers in the DRG. In conclusion, the current study demonstrates the neuroprotective effect of Red Sea sponge X. testudinaria extract against experimentally induced DPN through its antioxidant and anti-inflammatory mechanisms. MDPI 2022-10-24 /pmc/articles/PMC9693000/ /pubmed/36355482 http://dx.doi.org/10.3390/ph15111309 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/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 (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Magadmi, Rania
Borouk, Kariman
Youssef, Diaa T. A.
Shaala, Lamiaa A.
Alrafiah, Aziza R.
Shaik, Rasheed A.
Alharthi, Sameer E.
Neuroprotective Effect of Red Sea Marine Sponge Xestospongia testudinaria Extract Using In Vitro and In Vivo Diabetic Peripheral Neuropathy Models
title Neuroprotective Effect of Red Sea Marine Sponge Xestospongia testudinaria Extract Using In Vitro and In Vivo Diabetic Peripheral Neuropathy Models
title_full Neuroprotective Effect of Red Sea Marine Sponge Xestospongia testudinaria Extract Using In Vitro and In Vivo Diabetic Peripheral Neuropathy Models
title_fullStr Neuroprotective Effect of Red Sea Marine Sponge Xestospongia testudinaria Extract Using In Vitro and In Vivo Diabetic Peripheral Neuropathy Models
title_full_unstemmed Neuroprotective Effect of Red Sea Marine Sponge Xestospongia testudinaria Extract Using In Vitro and In Vivo Diabetic Peripheral Neuropathy Models
title_short Neuroprotective Effect of Red Sea Marine Sponge Xestospongia testudinaria Extract Using In Vitro and In Vivo Diabetic Peripheral Neuropathy Models
title_sort neuroprotective effect of red sea marine sponge xestospongia testudinaria extract using in vitro and in vivo diabetic peripheral neuropathy models
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9693000/
https://www.ncbi.nlm.nih.gov/pubmed/36355482
http://dx.doi.org/10.3390/ph15111309
work_keys_str_mv AT magadmirania neuroprotectiveeffectofredseamarinespongexestospongiatestudinariaextractusinginvitroandinvivodiabeticperipheralneuropathymodels
AT boroukkariman neuroprotectiveeffectofredseamarinespongexestospongiatestudinariaextractusinginvitroandinvivodiabeticperipheralneuropathymodels
AT youssefdiaata neuroprotectiveeffectofredseamarinespongexestospongiatestudinariaextractusinginvitroandinvivodiabeticperipheralneuropathymodels
AT shaalalamiaaa neuroprotectiveeffectofredseamarinespongexestospongiatestudinariaextractusinginvitroandinvivodiabeticperipheralneuropathymodels
AT alrafiahazizar neuroprotectiveeffectofredseamarinespongexestospongiatestudinariaextractusinginvitroandinvivodiabeticperipheralneuropathymodels
AT shaikrasheeda neuroprotectiveeffectofredseamarinespongexestospongiatestudinariaextractusinginvitroandinvivodiabeticperipheralneuropathymodels
AT alharthisameere neuroprotectiveeffectofredseamarinespongexestospongiatestudinariaextractusinginvitroandinvivodiabeticperipheralneuropathymodels