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Systemic bee venom exerts anti-arthritic and anti-inflammatory properties in a rat model of arthritis

Bee venom (BV) is widely used as a traditional China medicine to treat various conditions, including rheumatoid arthritis (RA). The aim of the present study was to evaluate the effects of systemic BV (60 mg/kg) as an anti-arthritic natural product, compare it with Methotrexate and determine the poss...

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Autores principales: El-Tedawy, Doaa Mohamed, Abd-Alhaseeb, Mohammad Mahmoud, Helmy, Maged Wasfy, Ghoneim, Asser Ibrahim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: D.A. Spandidos 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403832/
https://www.ncbi.nlm.nih.gov/pubmed/32765859
http://dx.doi.org/10.3892/br.2020.1327
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author El-Tedawy, Doaa Mohamed
Abd-Alhaseeb, Mohammad Mahmoud
Helmy, Maged Wasfy
Ghoneim, Asser Ibrahim
author_facet El-Tedawy, Doaa Mohamed
Abd-Alhaseeb, Mohammad Mahmoud
Helmy, Maged Wasfy
Ghoneim, Asser Ibrahim
author_sort El-Tedawy, Doaa Mohamed
collection PubMed
description Bee venom (BV) is widely used as a traditional China medicine to treat various conditions, including rheumatoid arthritis (RA). The aim of the present study was to evaluate the effects of systemic BV (60 mg/kg) as an anti-arthritic natural product, compare it with Methotrexate and determine the possible underlying mechanisms of BV action using complete Freund's adjuvant-induced arthritic rats. The development of signs of RA signs (knee joint circumference and arthritis scoring index) was evaluated. Erythrocyte sedimentation rate, serum tumor necrosis factor-α (TNF-α) and serum interleukin-1β (IL-1β) levels were measured at the end of the study. Histopathological examination followed by immunostaining of NF-κB (P65) was performed on the affected knee joints. Additionally, in vitro cyclooxygenase (COX) inhibition activity, carrageenan paw edema test and acetic acid writhing tests were performed to evaluate the anti-inflammatory and analgesic effects of the assessed dose and compared with diclofenac. An acute toxicity test was performed to establish the safety of BV at high doses. The results of the present study highlighted the potential of systemic BV on preventing the development of signs of RA. BV also significantly reduced serum levels of TNF-α, IL-1β and NF-κB in the affected joints. In addition to its potent analgesic activity, BV exhibited favorable inhibitory activity of the COX pathway in both in vivo and in vitro models. Therefore, high dose administration of systemic BV displayed safe and promising anti-arthritic, anti-inflammatory and analgesic properties through regulation of different mechanisms associated with the pathogenesis of RA.
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spelling pubmed-74038322020-08-05 Systemic bee venom exerts anti-arthritic and anti-inflammatory properties in a rat model of arthritis El-Tedawy, Doaa Mohamed Abd-Alhaseeb, Mohammad Mahmoud Helmy, Maged Wasfy Ghoneim, Asser Ibrahim Biomed Rep Articles Bee venom (BV) is widely used as a traditional China medicine to treat various conditions, including rheumatoid arthritis (RA). The aim of the present study was to evaluate the effects of systemic BV (60 mg/kg) as an anti-arthritic natural product, compare it with Methotrexate and determine the possible underlying mechanisms of BV action using complete Freund's adjuvant-induced arthritic rats. The development of signs of RA signs (knee joint circumference and arthritis scoring index) was evaluated. Erythrocyte sedimentation rate, serum tumor necrosis factor-α (TNF-α) and serum interleukin-1β (IL-1β) levels were measured at the end of the study. Histopathological examination followed by immunostaining of NF-κB (P65) was performed on the affected knee joints. Additionally, in vitro cyclooxygenase (COX) inhibition activity, carrageenan paw edema test and acetic acid writhing tests were performed to evaluate the anti-inflammatory and analgesic effects of the assessed dose and compared with diclofenac. An acute toxicity test was performed to establish the safety of BV at high doses. The results of the present study highlighted the potential of systemic BV on preventing the development of signs of RA. BV also significantly reduced serum levels of TNF-α, IL-1β and NF-κB in the affected joints. In addition to its potent analgesic activity, BV exhibited favorable inhibitory activity of the COX pathway in both in vivo and in vitro models. Therefore, high dose administration of systemic BV displayed safe and promising anti-arthritic, anti-inflammatory and analgesic properties through regulation of different mechanisms associated with the pathogenesis of RA. D.A. Spandidos 2020-10 2020-07-09 /pmc/articles/PMC7403832/ /pubmed/32765859 http://dx.doi.org/10.3892/br.2020.1327 Text en Copyright: © El-Tedawy et al. This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which permits use and distribution in any medium, provided the original work is properly cited, the use is non-commercial and no modifications or adaptations are made.
spellingShingle Articles
El-Tedawy, Doaa Mohamed
Abd-Alhaseeb, Mohammad Mahmoud
Helmy, Maged Wasfy
Ghoneim, Asser Ibrahim
Systemic bee venom exerts anti-arthritic and anti-inflammatory properties in a rat model of arthritis
title Systemic bee venom exerts anti-arthritic and anti-inflammatory properties in a rat model of arthritis
title_full Systemic bee venom exerts anti-arthritic and anti-inflammatory properties in a rat model of arthritis
title_fullStr Systemic bee venom exerts anti-arthritic and anti-inflammatory properties in a rat model of arthritis
title_full_unstemmed Systemic bee venom exerts anti-arthritic and anti-inflammatory properties in a rat model of arthritis
title_short Systemic bee venom exerts anti-arthritic and anti-inflammatory properties in a rat model of arthritis
title_sort systemic bee venom exerts anti-arthritic and anti-inflammatory properties in a rat model of arthritis
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7403832/
https://www.ncbi.nlm.nih.gov/pubmed/32765859
http://dx.doi.org/10.3892/br.2020.1327
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