Title : DHA Supplementation Attenuates MI-Induced LV Matrix Remodeling and Dysfunction in Mice.

Pub. Date : 2020

PMID : 32832005






4 Functional Relationships(s)
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1 Cardiac function was assessed using a pressure-volume catheter for up to 14 d. Results: DHA supplementation significantly attenuated the induction of peroxisome proliferator-activated receptor-alpha (PPAR-alpha) (2.3 +- 0.4 CD vs. 1.4 +- 0.3 DHA) after LAD occlusion. Docosahexaenoic Acids peroxisome proliferator activated receptor alpha Mus musculus
2 Cardiac function was assessed using a pressure-volume catheter for up to 14 d. Results: DHA supplementation significantly attenuated the induction of peroxisome proliferator-activated receptor-alpha (PPAR-alpha) (2.3 +- 0.4 CD vs. 1.4 +- 0.3 DHA) after LAD occlusion. Docosahexaenoic Acids peroxisome proliferator activated receptor alpha Mus musculus
3 Cardiac function was assessed using a pressure-volume catheter for up to 14 d. Results: DHA supplementation significantly attenuated the induction of peroxisome proliferator-activated receptor-alpha (PPAR-alpha) (2.3 +- 0.4 CD vs. 1.4 +- 0.3 DHA) after LAD occlusion. Docosahexaenoic Acids peroxisome proliferator activated receptor alpha Mus musculus
4 DHA seems to attenuate MI-induced cardiomyocyte injury partly by transient PPAR-alpha downregulation, diminishing the need for antioxidant mechanisms including mitochondrial function, or alpha- to beta-MHC isoform switch. Docosahexaenoic Acids peroxisome proliferator activated receptor alpha Mus musculus