Literature DB >> 12755383

Administration of the non-steroidal anti-inflammatory drug ibuprofen increases macrophage concentrations but reduces necrosis during modified muscle use.

E V Cheung1, J G Tidball.   

Abstract

OBJECTIVE: To test the hypothesis that ibuprofen administration during modified muscle use reduces muscle necrosis and invasion by select myeloid cell populations.
METHODS: Rats were subjected to hindlimb unloading for 10 days, after which they experienced muscle reloading by normal weight-bearing to induce muscle inflammation and necrosis. Some animals received ibuprofen by intraperitoneal injection 8 h prior to the onset of muscle reloading, and then again at 8 and 16 h following the onset of reloading. Other animals received buffer injection at 8 h prior to reloading and then ibuprofen at 8 and 16 h following the onset of reloading. Control animals received buffer only at each time point. Quantitative immunohistochemical analysis was used to assess the presence of necrotic muscle fibers, total inflammatory infiltrate, neutrophils, ED1+ macrophages and ED2+ macrophages at 24 h following the onset of reloading. RESULT: Administration of ibuprofen beginning 8 h prior to reloading caused significant reduction in the concentration of necrotic fibers, but increased the concentration of inflammatory cells in muscle. The increase in inflammatory cells was attributable to a 2.6-fold increase in the concentration of ED2+ macrophages. Animals treated with ibuprofen 8 h following the onset of reloading showed no decrease in muscle necrosis or increase in ED2+ macrophage concentrations.
CONCLUSION: Administration of ibuprofen prior to increased muscle loading reduces muscle damage, but increases the concentration of macrophages that express the ED2 antigen. The increase in ED2+ macrophage concentration and decrease in necrosis may be mechanistically related because ED2+ macrophages have been associated with muscle regeneration and repair.

Entities:  

Keywords:  NASA Discipline Musculoskeletal; NASA Program Fundamental Space Biology; Non-NASA Center

Mesh:

Substances:

Year:  2003        PMID: 12755383     DOI: 10.1007/s000110300068

Source DB:  PubMed          Journal:  Inflamm Res        ISSN: 1023-3830            Impact factor:   4.575


  10 in total

1.  Amelioration of Duchenne muscular dystrophy in mdx mice by elimination of matrix-associated fibrin-driven inflammation coupled to the αMβ2 leukocyte integrin receptor.

Authors:  Berta Vidal; Esther Ardite; Mònica Suelves; Vanessa Ruiz-Bonilla; Anna Janué; Matthew J Flick; Jay L Degen; Antonio L Serrano; Pura Muñoz-Cánoves
Journal:  Hum Mol Genet       Date:  2012-03-01       Impact factor: 6.150

2.  Is there an association between prior anti-inflammatory drug exposure and occurrence of peritonsillar abscess (PTA)? A national multicenter prospective observational case-control study.

Authors:  D Lepelletier; V Pinaud; P Le Conte; C Bourigault; N Asseray; F Ballereau; J Caillon; C Ferron; C Righini; E Batard; G Potel
Journal:  Eur J Clin Microbiol Infect Dis       Date:  2016-09-07       Impact factor: 3.267

3.  Degenerative and regenerative features of myofibers differ among skeletal muscles in a murine model of muscular dystrophy.

Authors:  Teppei Ikeda; Osamu Ichii; Saori Otsuka-Kanazawa; Teppei Nakamura; Yaser Hosny Ali Elewa; Yasuhiro Kon
Journal:  J Muscle Res Cell Motil       Date:  2016-07-29       Impact factor: 2.698

4.  The effects of MyD88 deficiency on disease phenotype in dysferlin-deficient A/J mice: role of endogenous TLR ligands.

Authors:  Kitipong Uaesoontrachoon; Hee-Jae Cha; Beryl Ampong; Arpana Sali; Jack Vandermeulen; Benjamin Wei; Brittany Creeden; Tony Huynh; James Quinn; Kathleen Tatem; Sree Rayavarapu; Eric P Hoffman; Kanneboyina Nagaraju
Journal:  J Pathol       Date:  2013-10       Impact factor: 7.996

5.  NS-398, a cyclooxygenase-2-specific inhibitor, delays skeletal muscle healing by decreasing regeneration and promoting fibrosis.

Authors:  Wei Shen; Yong Li; Ying Tang; James Cummins; Johnny Huard
Journal:  Am J Pathol       Date:  2005-10       Impact factor: 4.307

6.  Use of pifithrin to inhibit p53-mediated signalling of TNF in dystrophic muscles of mdx mice.

Authors:  Felicity J Waters; Thea Shavlakadze; Matthew J McIldowie; Matthew J Piggott; Miranda D Grounds
Journal:  Mol Cell Biochem       Date:  2009-10-27       Impact factor: 3.396

Review 7.  The inflammatory response to skeletal muscle injury: illuminating complexities.

Authors:  Carine Smith; Maritza J Kruger; Robert M Smith; Kathryn H Myburgh
Journal:  Sports Med       Date:  2008       Impact factor: 11.136

8.  Nonsteroidal anti-inflammatory drug use and the risk of severe skin and soft tissue complications in patients with varicella or zoster disease.

Authors:  Yann Mikaeloff; Abbas Kezouh; Samy Suissa
Journal:  Br J Clin Pharmacol       Date:  2008-02       Impact factor: 4.335

9.  Modulation of Klotho expression in injured muscle perturbs Wnt signalling and influences the rate of muscle growth.

Authors:  Steven S Welc; Michelle Wehling-Henricks; Makoto Kuro-O; Kyle A Thomas; James G Tidball
Journal:  Exp Physiol       Date:  2019-12-16       Impact factor: 2.969

Review 10.  Key concepts in muscle regeneration: muscle "cellular ecology" integrates a gestalt of cellular cross-talk, motility, and activity to remodel structure and restore function.

Authors:  Judy E Anderson
Journal:  Eur J Appl Physiol       Date:  2021-12-20       Impact factor: 3.078

  10 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.