Capsaicinoids improve consequences of physical activity

  • Toxicol Rep. 2018 May 15:5:598-607. doi: 10.1016/j.toxrep.2018.05.001.
Kazim Sahin  1 ,  Cemal Orhan  1 ,  Mehmet Tuzcu  2 ,  Nurhan Sahin  1 ,  Fusun Erten  2 ,  Vijaya Juturu  3
Affiliations
  • 1. Department of Animal Nutrition, Faculty of Veterinary Science, Firat University, Elazig, Turkey.
  • 2. Division of Biology, Faculty of Science, Firat University, Elazig, Turkey.
  • 3. Research and Development, Clinical Affairs, OmniActive Health Technologies Inc., Morristown, NJ, USA.
PMID: 29854630 DOI: 10.1016/j.toxrep.2018.05.001
Abstract

The purpose of this study was to investigate the effects of capsaicinoids (CAPs) on lipid metabolism, inflammation, antioxidant status and the changes in gene products involved in these metabolic functions in exercised rats. A total of 28 male Wistar albino rats were randomly divided into four groups (n = 7) (i) No exercise and no CAPs, (ii) No exercise + CAPs (iii) Regular exercise, (iv) Regular exercise + CAPs. Rats were administered as 0.2 mg capsaicinoids from 10 mg/kg BW/day Capsimax® daily for 8 weeks. A significant decrease in lactate and malondialdehyde (MDA) levels and increase in activities of antioxidant Enzymes were observed in the combination of regular exercise and CAPs group (P < 0.0001). Regular exercise + CAPs treated rats had greater nuclear factor-E2-related factor-2 (Nrf2) and heme oxygenase-1 (HO-1) levels in muscle than regular exercise and no exercise rats (P < 0.001). Nevertheless, regular exercise + CAPs treated had lower nuclear factor kappa B (NF-κB) and IL-10 levels in muscle than regular exercise and control rats (P < 0.001). Muscle sterol regulatory element-binding protein 1c (SREBP-1c), liver X receptors (LXR), ATP Citrate Lyase (ACLY) and fatty acid synthase (FAS) levels in the regular exercise + CAPs group were lower than all groups (P < 0.05). However, muscle PPAR-γ level was higher in the regular exercise and CAPs alone than the no exercise rats. These results suggest CAPs with regular exercise may enhance lipid metabolism by regulation of gene products involved in lipid and antioxidant metabolism including SREBP-1c, PPAR-γ, and Nrf2 pathways in rats.

Keywords
ACLY, ATP-citrate lyase; ACS, acetyl-CoA synthetase; AMPK, phosphorylated AMP-activated protein kinase; ARE, antioxidant response element; CAPs, capsaicinoids; Capsaicinoid; Exercise; FAS, fatty acid synthase; GSH-Px, glutathione peroxidase; HO-1, heme-oxygenase 1; IL-10, interleukin-10; LXR-s, liver X receptor-s; MDA, malondialdehyde; MMP-9, matrix metalloproteinase-9; NF-κB, nuclear factor kappa-light-chain-enhancer of activated B cells; Nrf2; Nrf2, nuclear factor (erythroid-derived 2)-like 2; PGC-la, peroxisomal proliferator activator receptor c coactivator; PPAR-γ; PPAR-γ, peroxisome proliferator-activated receptor gamma; ROS, reactive oxygen species; SOD, superoxide dismutase; SREBP-1c; SREBP-1c, sterol regulatory element-binding protein1c; TC, total serum cholesterol; TG, triglyceride; TNF-α, tumor necrosis factor-α; TRPV1, transient receptor potential vanilloid subtype 1; Tfam, mitochondrial transcription factor A.
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