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Exercise training increased gene expression of LDL-R and PCSK9 in intestine: link to transintestinal cholesterol excretion. | LitMetric

AI Article Synopsis

  • The study investigates how exercise training affects the intestinal receptors that play a role in transintestinal cholesterol excretion (TICE) in both regular and ovariectomized (Ovx) rats.
  • Researchers divided Sprague-Dawley rats into four groups based on diet (standard vs. high cholesterol) and measured the impact of exercise over six weeks.
  • Results showed that exercise increased the expression of key intestinal receptors (LDL-R and PCSK9) involved in cholesterol uptake, suggesting that physical activity could help eliminate cholesterol via TICE pathways in both types of rats.

Article Abstract

Transintestinal cholesterol excretion (TICE) is known as an alternate non-biliary route of cholesterol excretion from the body. The aim of this study was to determine whether exercise training has effects on intestinal membrane receptors involved in TICE in intact and ovariectomized (Ovx) rats. Sprague-Dawley rats were first divided into 4 groups: Sham operated and Ovx rats fed a standard diet (Sham-SD; Ovx-SD), or a high cholesterol diet (Sham-Chol; Ovx-Chol). These 4 groups were subsequently subdivided into either sedentary or voluntary wheel running groups for 6 weeks. The cholesterol diet resulted in increased hepatic cholesterol accumulation (p< 0.001) in both Sham and Ovx rats. Exercise training increased (p < 0.01) transcripts of intestinal low density lipoprotein receptor (LDL-R) and proprotein convertase subtilisin/kexin type 9 (PCSK9), which are involved in trans-intestinal cholesterol uptake from circulation, in both Sham and Ovx rats compared to rats remaining sedentary in all diet conditions. The up-regulation of intestinal gene expression of LDL-R and PCSK9 following voluntary wheel running in intact and Ovx rats suggests that exercise training may contribute to elimination of cholesterol through the TICE pathway.

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Source
http://dx.doi.org/10.4149/gpb_2017047DOI Listing

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