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Furthermore, at physiological concentrations, nitric oxide ( NO) is considered neuroprotective due to its role in vasodilation and neurotransmission [19]

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One hallmark feature of OA-related subchondral bone pathology in early stages is the disruption of its architecture, including the formation of bone marrow lesions (BMLs), microcracks, diffuse microdamage, and marginal osteophytes

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