The Statin Target HMG-Coenzyme a Reductase (Hmgcr) Regulates Sleep Homeostasis in Drosophila

Statins, HMG Coenzyme A Reductase (HMGCR) inhibitors, are a first-line therapy, used to reduce hypercholesterolemia and the risk for cardiovascular events. While sleep disturbances are recognized as a side-effect of statin treatment, the impact of statins on sleep is under debate. Using Drosophila,...

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Veröffentlicht in:Pharmaceuticals (Basel, Switzerland) Switzerland), 2022-01, Vol.15 (1), p.79
Hauptverfasser: Alsehli, Ahmed M, Liao, Sifang, Al-Sabri, Mohamed H, Vasionis, Lukas, Purohit, Archana, Behare, Neha, Clemensson, Laura E, Williams, Michael J, Schiöth, Helgi B
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Sprache:eng
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Zusammenfassung:Statins, HMG Coenzyme A Reductase (HMGCR) inhibitors, are a first-line therapy, used to reduce hypercholesterolemia and the risk for cardiovascular events. While sleep disturbances are recognized as a side-effect of statin treatment, the impact of statins on sleep is under debate. Using Drosophila, we discovered a novel role for Hmgcr in sleep modulation. Loss of pan-neuronal expression affects fly sleep behavior, causing a decrease in sleep latency and an increase in sleep episode duration. We localized the (PI), equivalent to the mammalian hypothalamus, as the region within the fly brain requiring Hmgcr activity for proper sleep maintenance. Lack of expression in the PI insulin-producing cells recapitulates the sleep effects of pan-neuronal knockdown. Conversely, loss of in a different PI subpopulation, the corticotropin releasing factor (CRF) homologue-expressing neurons (DH44 neurons), increases sleep latency and decreases sleep duration. The requirement for Hmgcr activity in different neurons signifies its importance in sleep regulation. Interestingly, loss of in the PI does not affect circadian rhythm, suggesting that Hmgcr regulates sleep by pathways distinct from the circadian clock. Taken together, these findings suggest that Hmgcr activity in the PI is essential for proper sleep homeostasis in flies.
ISSN:1424-8247
1424-8247
DOI:10.3390/ph15010079