Run to Remember: A Mouse-Model Study Investigating the Mechanism of Exercise-Induced Neuroprotection

Research in animal models shows physical exercise can induce changes in the brain. In humans, studies also revealed changes in brain physiology and function resulting from physical exercise, including increased hippocampal and cognitive performance (1). Several studies in mice and rats also demonstrated that exercise can improve learning and memory and decrease neuroinflammation in models of Alzheimer’s disease and other neurodegenerative pathologies (2); these benefits are tied to increased plasticity and decreased inflammation in the hippocampus in mice (2). If regular time pounding the pavement does improve brain function, what is the underlying molecular biology of exercise-induced neuroprotection? Can we identify the cellular pathways and components involved? Can we detect important components in blood plasma? And, is the benefit of these components transferrable between organisms? De Miguel and colleagues set out to answer these questions and describe their results in a recent study published in Nature.

A recent study investigates the underlying molecular mechanisms of exercise-induced neuroprotection in a mouse model.
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Insights into the Function of P7C3 Compounds in Neuroprotection

The multiple Lombardi trophies won by Pittsburgh Steelers.  Image used under Wikimedia Creative Commons, and attributed to daveynin.
The multiple Lombardi trophies won by Pittsburgh Steelers. Image used under Wikimedia Creative Commons, and attributed to daveynin.

It is fall and the season for American football. For this football fan, watching the game is a bit less enjoyable than it used to be, asย more and more information is available about the serious and permanent brain injuries suffered by football players.

In the introduction to a recent paper in the journal Cell, โ€œP7C3 Neuroprotective Chemicals Function by Activating the Rate-Limiting Enzyme in NAD Salvageโ€, not a word about American football is mentioned.

However, the paper begins, โ€œNo substantive therapeutics are available for the treatment of almost any form of disease entailing nerve deathโ€ (1). The authors list a range of neurodegenerative disorders such as Huntingtonโ€™s, Alzheimers and Parkinsonโ€™s diseases, as well as ALSย  or Lou Gherig’s disease. They also note that there are currently no effective treatments for trauma to the brain or peripheral nervous system.

The authors note that a chemical treatment that could interfere with nerve cell death would have a โ€œtransformative impact in modern medicineโ€. Continue reading “Insights into the Function of P7C3 Compounds in Neuroprotection”