Sulforaphane inhibits hepatic steatosis in rats by down-regulating DGAT2 and ACAT1 expression

Objective To study the effects of sulforaphane (SFN) on the deposition of lipid droplets and the expression of their peripheral proteins in the liver and elucidate the mechanism by which SFN inhibits non-alcoholic fatty liver caused by high-fat diet. Methods Sixty male Wistar rats were randomized in...

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Main Authors: TIAN Sicong, LEI Peng, SUN Yao
Format: Article
Language:zho
Published: Editorial Office of Journal of Third Military Medical University 2019-06-01
Series:Di-san junyi daxue xuebao
Subjects:
Online Access:http://aammt.tmmu.edu.cn/Upload/rhtml/201812039.htm
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author TIAN Sicong
LEI Peng
SUN Yao
author_facet TIAN Sicong
LEI Peng
SUN Yao
author_sort TIAN Sicong
collection DOAJ
description Objective To study the effects of sulforaphane (SFN) on the deposition of lipid droplets and the expression of their peripheral proteins in the liver and elucidate the mechanism by which SFN inhibits non-alcoholic fatty liver caused by high-fat diet. Methods Sixty male Wistar rats were randomized into 6 equal groups (n=10), includinganormal food group, ahigh-fat diet group, 3 high-fat diet groups treated with high (20 mg/kg), moderate (10 mg/kg) and low (5 mg/kg) doses of SFN, andahigh-fat diet group treated withapositive drug (30 mg/kg). Triglyceride and total cholesterol contents were examined and the deposition of lipid droplets in the liver was detected with oil redOstaining in all the rats. The protein expression of DGAT2 and ACAT1 (the key synthases of triglyceride and cholesterol, respectively) in the liver tissues were detected with Western blotting; immunohistochemistry and real-time PCR were performed to examine the expression of the PAT proteins (PLIN1, PLIN2, PLIN3 and PLIN5) at both the protein and mRNA levels in the liver. Results SFN treatment obviously reduced high-fat diet-induced bodyweight gain in the rats, lowered the levels of triglyceride and total cholesterol, lessened lipid droplet deposition in the liver and reduced the volume of the lipid droplets. Treatment with SFN at all the 3 doses significantly down-regulated the expression of ACAT1 and DGAT2 in the liver of the rats (P < 0.01). SFN at the high doses significantly down-regulated the expression of PLIN2 and PLIN5 in liver tissue at both the mRNA and protein levels (P < 0.01, P < 0.05). Conclusion SFN can inhibit the formation of lipid droplets by reducing the expressions of DGAT2, ACAT1, PLIN2 and PLIN5 in the liver of rats.
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spelling doaj.art-779a2b09aafb4fb9a5ee7c838f54e0182022-12-21T18:43:00ZzhoEditorial Office of Journal of Third Military Medical UniversityDi-san junyi daxue xuebao1000-54042019-06-0141121102110910.16016/j.1000-5404.201812039Sulforaphane inhibits hepatic steatosis in rats by down-regulating DGAT2 and ACAT1 expressionTIAN Sicong0LEI Peng1SUN Yao2Faculty of Food Science and Engineering, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin, Heilongjiang Province, 150001Faculty of Food Science and Engineering, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin, Heilongjiang Province, 150001Faculty of Food Science and Engineering, School of Chemistry and Chemical Engineering, Harbin Institute of Technology, Harbin, Heilongjiang Province, 150001Objective To study the effects of sulforaphane (SFN) on the deposition of lipid droplets and the expression of their peripheral proteins in the liver and elucidate the mechanism by which SFN inhibits non-alcoholic fatty liver caused by high-fat diet. Methods Sixty male Wistar rats were randomized into 6 equal groups (n=10), includinganormal food group, ahigh-fat diet group, 3 high-fat diet groups treated with high (20 mg/kg), moderate (10 mg/kg) and low (5 mg/kg) doses of SFN, andahigh-fat diet group treated withapositive drug (30 mg/kg). Triglyceride and total cholesterol contents were examined and the deposition of lipid droplets in the liver was detected with oil redOstaining in all the rats. The protein expression of DGAT2 and ACAT1 (the key synthases of triglyceride and cholesterol, respectively) in the liver tissues were detected with Western blotting; immunohistochemistry and real-time PCR were performed to examine the expression of the PAT proteins (PLIN1, PLIN2, PLIN3 and PLIN5) at both the protein and mRNA levels in the liver. Results SFN treatment obviously reduced high-fat diet-induced bodyweight gain in the rats, lowered the levels of triglyceride and total cholesterol, lessened lipid droplet deposition in the liver and reduced the volume of the lipid droplets. Treatment with SFN at all the 3 doses significantly down-regulated the expression of ACAT1 and DGAT2 in the liver of the rats (P < 0.01). SFN at the high doses significantly down-regulated the expression of PLIN2 and PLIN5 in liver tissue at both the mRNA and protein levels (P < 0.01, P < 0.05). Conclusion SFN can inhibit the formation of lipid droplets by reducing the expressions of DGAT2, ACAT1, PLIN2 and PLIN5 in the liver of rats.http://aammt.tmmu.edu.cn/Upload/rhtml/201812039.htmsulforaphanetriglyceridecholesterollipid dropletsdgat2acat1plin2plin5
spellingShingle TIAN Sicong
LEI Peng
SUN Yao
Sulforaphane inhibits hepatic steatosis in rats by down-regulating DGAT2 and ACAT1 expression
Di-san junyi daxue xuebao
sulforaphane
triglyceride
cholesterol
lipid droplets
dgat2
acat1
plin2
plin5
title Sulforaphane inhibits hepatic steatosis in rats by down-regulating DGAT2 and ACAT1 expression
title_full Sulforaphane inhibits hepatic steatosis in rats by down-regulating DGAT2 and ACAT1 expression
title_fullStr Sulforaphane inhibits hepatic steatosis in rats by down-regulating DGAT2 and ACAT1 expression
title_full_unstemmed Sulforaphane inhibits hepatic steatosis in rats by down-regulating DGAT2 and ACAT1 expression
title_short Sulforaphane inhibits hepatic steatosis in rats by down-regulating DGAT2 and ACAT1 expression
title_sort sulforaphane inhibits hepatic steatosis in rats by down regulating dgat2 and acat1 expression
topic sulforaphane
triglyceride
cholesterol
lipid droplets
dgat2
acat1
plin2
plin5
url http://aammt.tmmu.edu.cn/Upload/rhtml/201812039.htm
work_keys_str_mv AT tiansicong sulforaphaneinhibitshepaticsteatosisinratsbydownregulatingdgat2andacat1expression
AT leipeng sulforaphaneinhibitshepaticsteatosisinratsbydownregulatingdgat2andacat1expression
AT sunyao sulforaphaneinhibitshepaticsteatosisinratsbydownregulatingdgat2andacat1expression