Publications by authors named "S Buvinic"

Oxidative stress and the activation of the nucleotide-binding domain, leucine-rich-containing family, pyrin domain containing 3 (NLRP3) inflammasome have been linked to insulin resistance in skeletal muscle. In immune cells, the exacerbated generation of reactive oxygen species (ROS) activates the NLRP3 inflammasome, by facilitating the interaction between thioredoxin interacting protein (TXNIP) and NLRP3. However, the precise role of ROS/TXNIP-dependent NLRP3 inflammasome activation in skeletal muscle during obesity-induced insulin resistance remains undefined.

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Article Synopsis
  • Adult mice are used in mandibular dynamics studies because their chewing patterns are similar to humans; researchers used botulinum toxin type A (BoNTA) to induce muscle atrophy in one masseter muscle and studied its effects.
  • After BoNTA treatment, there was a significant increase in atrophy-related gene expression and a reduction in muscle size, particularly in the masseter, temporalis, and medial pterygoid muscles, observed at 14 days.
  • The study concluded that impairment of one masticatory muscle affects not only the treated muscle but also its agonistic counterpart, highlighting the interconnectedness of the masticatory system and the need for further clinical research.
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Fibroblast growth factor 21 (FGF21) is a hormone involved in the regulation of lipid, glucose, and energy metabolism. Although it is released mainly from the liver, in recent years it has been shown that it is a "myokine", synthesized in skeletal muscles after exercise and stress conditions through an Akt-dependent pathway and secreted for mediating autocrine and endocrine roles. To date, the molecular mechanism for the pathophysiological regulation of FGF21 production in skeletal muscle is not totally understood.

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Muscle and bone are tightly integrated through mechanical and biochemical signals. Osteoclasts are cells mostly related to pathological bone loss; however, they also start physiological bone remodeling. Therefore, osteoclast signals released during bone remodeling could improve both bone and skeletal muscle mass.

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One of the most important functions of skeletal muscle is to respond to nerve stimuli by contracting. This function ensures body movement but also participates in other important physiological roles, like regulation of glucose homeostasis. Muscle activity is closely regulated to adapt to different demands and shows a plasticity that relies on both transcriptional activity and nerve stimuli.

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