Literature DB >> 33668129

Early Lipid Raft-Related Changes: Interplay between Unilateral Denervation and Hindlimb Suspension.

Irina G Bryndina1, Maria N Shalagina1, Vladimir A Protopopov1, Alexey V Sekunov1, Andrey L Zefirov2, Guzalia F Zakirjanova2,3, Alexey M Petrov2,3.   

Abstract

Muscle disuse and denervation leads to muscle atrophy, but underlying mechanisms can be different. Previously, we have found ceramide (Cer) accumulation and lipid raft disruption after acute hindlimb suspension (HS), a model of muscle disuse. Herein, using biochemical and fluorescent approaches the influence of unilateral denervation itself and in combination with short-term HS on membrane-related parameters of rat soleus muscle was studied. Denervation increased immunoexpression of sphingomyelinase and Cer in plasmalemmal regions, but decreased Cer content in the raft fraction and enhanced lipid raft integrity. Preliminary denervation suppressed (1) HS-induced Cer accumulation in plasmalemmal regions, shown for both nonraft and raft-fractions; (2) HS-mediated decrease in lipid raft integrity. Similar to denervation, inhibition of the sciatic nerve afferents with capsaicin itself increased Cer plasmalemmal immunoexpression, but attenuated the membrane-related effects of HS. Finally, both denervation and capsaicin treatment increased immunoexpression of proapoptotic protein Bax and inhibited HS-driven increase in antiapoptotic protein Bcl-2. Thus, denervation can increase lipid raft formation and attenuate HS-induced alterations probably due to decrease of Cer levels in the raft fraction. The effects of denervation could be at least partially caused by the loss of afferentation. The study points to the importance of motor and afferent inputs in control of Cer distribution and thereby stability of lipid rafts in the junctional and extrajunctional membranes of the muscle.

Entities:  

Keywords:  acid sphingomyelinase; apoptotic proteins; capsaicin; ceramide; deafferentation; denervation; disuse; lipid rafts; neuromuscular junction; skeletal muscle

Mesh:

Substances:

Year:  2021        PMID: 33668129      PMCID: PMC7956661          DOI: 10.3390/ijms22052239

Source DB:  PubMed          Journal:  Int J Mol Sci        ISSN: 1422-0067            Impact factor:   5.923


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