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. 2022 Sep 9;14(18):3718. doi: 10.3390/nu14183718

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© 2022 by the authors.

Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

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P-PCs and P-OPCs administration improves hepatic lipid accumulation and adipose tissue development. C57BL/6 mice were fed a HFD with the administration of P-PCs and P-OPCs. (a) H&E stained liver sections and epididymal adipose tissue; (b–d) weight of perirenal fat mass, epididymal fat mass and inguinal fat mass in different treatment groups; (e) Adipocyte size area of epididymal fat mass; (f,g) Liver weights and liver lipids accumulation in different group. Hepatic lipids were extracted by homogenizing the liver tissue in chloroform/methanol lipid extraction buffer and were analyzed according to the manufacturer’s protocol. The results were analyzed with a one-way ANOVA with Tukey’s Multiple Comparison Test using GraphPad Prism ver. 5.1 software. * p < 0.05, ** p < 0.01. # p < 0.05 between PPCs and POPCs.

P-PCs and P-OPCs administration improves hepatic lipid accumulation and adipose tissue development. C57BL/6 mice were fed a HFD with the administration of P-PCs and P-OPCs. (a) H&E stained liver sections and epididymal adipose tissue; (b–d) weight of perirenal fat mass, epididymal fat mass and inguinal fat mass in different treatment groups; (e) Adipocyte size area of epididymal fat mass; (f,g) Liver weights and liver lipids accumulation in different group. Hepatic lipids were extracted by homogenizing the liver tissue in chloroform/methanol lipid extraction buffer and were analyzed according to the manufacturer’s protocol. The results were analyzed with a one-way ANOVA with Tukey’s Multiple Comparison Test using GraphPad Prism ver. 5.1 software. * p < 0.05, ** p < 0.01. # p < 0.05 between PPCs and POPCs.