Effect of oxytocin on lipid accumulation under inflammatory conditions in human macrophages

Oxytocin (OT) is a neuropeptide hormone secreted by the posterior pituitary gland. Deficits in OT action have been observed in patients with behavioral and mood disorders, some of which correlate with an increased risk of cardiovascular disease (CVD). Recent research has revealed a wider systemic ro...

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Veröffentlicht in:Experimental and molecular pathology 2021-02, Vol.118, p.104604, Article 104604
Hauptverfasser: Karten, Ariel, Vernice, Nicholas A., Renna, Heather A., Carsons, Steven E., DeLeon, Joshua, Pinkhasov, Aaron, Gomolin, Irving H., Glass, Daniel S., Reiss, Allison B., Kasselman, Lora J.
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Sprache:eng
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Zusammenfassung:Oxytocin (OT) is a neuropeptide hormone secreted by the posterior pituitary gland. Deficits in OT action have been observed in patients with behavioral and mood disorders, some of which correlate with an increased risk of cardiovascular disease (CVD). Recent research has revealed a wider systemic role that OT plays in inflammatory modulation and development of atherosclerotic plaques. This study investigated the role that OT plays in cholesterol transport and foam cell formation in LPS-stimulated THP-1 human macrophages. THP-1 differentiated macrophages were treated with media, LPS (100 ng/ml), LPS + OT (10 pM), or LPS + OT (100 pM). Changes in gene expression and protein levels of cholesterol transporters were analyzed by real time quantitative PCR (RT-qPCR) and Western blot, while oxLDL uptake and cholesterol efflux capacity were evaluated with fluorometric assays. RT-qPCR analysis revealed a significant increase in ABCG1 gene expression upon OT + LPS treatment, compared to LPS alone (p = 0.0081), with Western blotting supporting the increase in expression of the ABCG1 protein. Analysis of oxLDL uptake showed a significantly lower fluorescent value in LPS + OT (100pM) -treated cells when compared to LPS alone (p 
ISSN:0014-4800
1096-0945
DOI:10.1016/j.yexmp.2021.104604