Abstract

Insights into the effects of osteoarthritis (OA) and physical interventions on the musculoskeletal system are limited. Our goal was to analyze musculoskeletal changes in OA mice and test the efficacy of 8-week exposure to hypergravity, as a replacement of physical activity. 16-week-old male (C57BL/6J) mice allocated to sham control and OA groups not centrifuged (Ctrl 1g and OA 1g, respectively) or centrifuged at 2g acceleration (Ctrl 2g and OA 2g). OA 1g displayed decreased trabecular bone in the proximal tibia metaphysis and increased osteoclastic activity and local TNFα gene expression, all entirely prevented by 2g gravitational therapy. However, while cortical bone of tibia midshaft was preserved in OA 1g (vs. ctrl), it is thinner in OA 2g (vs. OA 1g). In the hind limb, OA at 1g increased fibers with lipid droplets by 48% in the tibialis anterior, a fact fully prevented by 2g. In Ctrl, 2g increased soleus, tibialis anterior and gastrocnemius masses. In the soleus of both Ctrl and OA, 2g induced larger fibers and a switch from type-II to type-I fiber. Catabolic (myostatin and its receptor activin RIIb and visfatine) and anabolic (FNDC5) genes dramatically increased in Ctrl 2g and OA 2g (p<0.01 vs 1g). Nevertheless, the overexpression of FNDC5 (and follistatine) was smaller in OA 2g than in Ctrl 2g. Thus, hypergravity in OA mice produced positive effects for trabecular bone and muscle typology, similar to resistance exercises, but negative effects for cortical bone.

Highlights

  • The hallmark of osteoarthritis (OA) is loss of articular cartilage, subchondral bone disturbances such as sclerotic changes and osteophyte growth [1, 2]

  • Following the destabilization of the medial meniscus, its medial displacement occurs, and weight is transmitted across a small area on the medial side, leading to increased local mechanical stress

  • At the proximal metaphysis, trabecular bone volume decreased due to reduced trabecular number, increased osteoclastic resorption, and increased local TNFα gene expression, a potent proinflammatory cytokine playing a crucial role in stimulating osteoclastogenesis [39]

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Summary

Introduction

The hallmark of osteoarthritis (OA) is loss of articular cartilage, subchondral bone disturbances such as sclerotic changes and osteophyte growth [1, 2]. OA patients have pain related to joint degeneration, inflammation and joint stiffness that reduce range of motion [4,5,6,7]. These disabilities can combine with depressive states and expose them to a negative spiral of accumulation of negative effects due to sedentary lifestyle.

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