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. 2015 Mar 17;7(3):1978–1991. doi: 10.3390/nu7031978

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© 2015 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 license (http://creativecommons.org/licenses/by/4.0/).

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Histology of epididymal adipose (A) and liver (C) tissues of mice fed experimental diets for six weeks (magnification= ×200). Normal-fat diet (NFD), high-fat diet (HFD), high-fat diet with 100 mg·kg⁻¹·day⁻¹ Allomirina dichotoma larva suspension (HFD + ADL 100), and HFD with 3000 mg·kg⁻¹·day⁻¹ ADL (HFD + ADL 3000). Epididymal adipose cell volume measured by IMT i-Solution Lite program (B). Histopathology of the liver with steatosis. Arrows indicate the macrovesicular lipid droplets in the cytoplasm of hepatocytes (C). Results are expressed as mean ± SD (n = 3). Statistical significance was evaluated by Duncan post-hoc test in ANOVA. p < 0.001 and p < 0.01, compared to the high-fat diet group.

Histology of epididymal adipose (A) and liver (C) tissues of mice fed experimental diets for six weeks (magnification= ×200). Normal-fat diet (NFD), high-fat diet (HFD), high-fat diet with 100 mg·kg⁻¹·day⁻¹ Allomirina dichotoma larva suspension (HFD + ADL 100), and HFD with 3000 mg·kg⁻¹·day⁻¹ ADL (HFD + ADL 3000). Epididymal adipose cell volume measured by IMT i-Solution Lite program (B). Histopathology of the liver with steatosis. Arrows indicate the macrovesicular lipid droplets in the cytoplasm of hepatocytes (C). Results are expressed as mean ± SD (n = 3). Statistical significance was evaluated by Duncan post-hoc test in ANOVA. p < 0.001 and p < 0.01, compared to the high-fat diet group.