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Polyherbal formulation PL02 alleviates pain, inflammation, and subchondral bone deterioration in an osteoarthritis rodent model
INTRODUCTION: Osteoarthritis (OA) is a debilitating disease with significant personal and socioeconomic burdens worldwide. METHODS: To address this, we developed a multitargeted formulation called PL02, which includes standardized extracts of Rosa canina L, Hippophae rhamnoides, and collagen peptide...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693428/ https://www.ncbi.nlm.nih.gov/pubmed/38045809 http://dx.doi.org/10.3389/fnut.2023.1217051 |
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author | Upadhyay, Prabhat Kalra, Diya Nilakhe, Aishwarya Shrikant Aggrawal, Vijay Gupta, Sarika |
author_facet | Upadhyay, Prabhat Kalra, Diya Nilakhe, Aishwarya Shrikant Aggrawal, Vijay Gupta, Sarika |
author_sort | Upadhyay, Prabhat |
collection | PubMed |
description | INTRODUCTION: Osteoarthritis (OA) is a debilitating disease with significant personal and socioeconomic burdens worldwide. METHODS: To address this, we developed a multitargeted formulation called PL02, which includes standardized extracts of Rosa canina L, Hippophae rhamnoides, and collagen peptide. We tested the pharmacological efficacy of PL02 in a rodent model of OA induced by Monosodium iodoacetate (MIA). RESULTS: Our results demonstrate that oral administration of PL02 has antioxidant effects by down-regulating NOS, reduces pain-related behavior, and mitigates inflammation by inhibiting IL-1b and TNF-α production, as well as downregulating CGRP1 and COX-II. PL02 also exhibits anti-catabolic and chondroprotective activity by significantly downregulating MMP13 and upregulating BCL2. Additionally, PL02 demonstrates chondrogenic activity by significantly upregulating SOX-9 (a master regulator of chondrogenesis), Coll-I, and aggrecan, which are major components of articular cartilage. Furthermore, PL02 prevents microarchitectural deterioration of subchondral bone. CONCLUSION: Overall, PL02 is an orally active, multi-targeted therapy that not only alleviates pain and inflammation but also effectively halts cartilage and subchondral bone deterioration. It represents a safe and promising candidate for the treatment and management of OA. |
format | Online Article Text |
id | pubmed-10693428 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-106934282023-12-03 Polyherbal formulation PL02 alleviates pain, inflammation, and subchondral bone deterioration in an osteoarthritis rodent model Upadhyay, Prabhat Kalra, Diya Nilakhe, Aishwarya Shrikant Aggrawal, Vijay Gupta, Sarika Front Nutr Nutrition INTRODUCTION: Osteoarthritis (OA) is a debilitating disease with significant personal and socioeconomic burdens worldwide. METHODS: To address this, we developed a multitargeted formulation called PL02, which includes standardized extracts of Rosa canina L, Hippophae rhamnoides, and collagen peptide. We tested the pharmacological efficacy of PL02 in a rodent model of OA induced by Monosodium iodoacetate (MIA). RESULTS: Our results demonstrate that oral administration of PL02 has antioxidant effects by down-regulating NOS, reduces pain-related behavior, and mitigates inflammation by inhibiting IL-1b and TNF-α production, as well as downregulating CGRP1 and COX-II. PL02 also exhibits anti-catabolic and chondroprotective activity by significantly downregulating MMP13 and upregulating BCL2. Additionally, PL02 demonstrates chondrogenic activity by significantly upregulating SOX-9 (a master regulator of chondrogenesis), Coll-I, and aggrecan, which are major components of articular cartilage. Furthermore, PL02 prevents microarchitectural deterioration of subchondral bone. CONCLUSION: Overall, PL02 is an orally active, multi-targeted therapy that not only alleviates pain and inflammation but also effectively halts cartilage and subchondral bone deterioration. It represents a safe and promising candidate for the treatment and management of OA. Frontiers Media S.A. 2023-11-16 /pmc/articles/PMC10693428/ /pubmed/38045809 http://dx.doi.org/10.3389/fnut.2023.1217051 Text en Copyright © 2023 Upadhyay, Kalra, Nilakhe, Aggrawal and Gupta. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Nutrition Upadhyay, Prabhat Kalra, Diya Nilakhe, Aishwarya Shrikant Aggrawal, Vijay Gupta, Sarika Polyherbal formulation PL02 alleviates pain, inflammation, and subchondral bone deterioration in an osteoarthritis rodent model |
title | Polyherbal formulation PL02 alleviates pain, inflammation, and subchondral bone deterioration in an osteoarthritis rodent model |
title_full | Polyherbal formulation PL02 alleviates pain, inflammation, and subchondral bone deterioration in an osteoarthritis rodent model |
title_fullStr | Polyherbal formulation PL02 alleviates pain, inflammation, and subchondral bone deterioration in an osteoarthritis rodent model |
title_full_unstemmed | Polyherbal formulation PL02 alleviates pain, inflammation, and subchondral bone deterioration in an osteoarthritis rodent model |
title_short | Polyherbal formulation PL02 alleviates pain, inflammation, and subchondral bone deterioration in an osteoarthritis rodent model |
title_sort | polyherbal formulation pl02 alleviates pain, inflammation, and subchondral bone deterioration in an osteoarthritis rodent model |
topic | Nutrition |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10693428/ https://www.ncbi.nlm.nih.gov/pubmed/38045809 http://dx.doi.org/10.3389/fnut.2023.1217051 |
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