Preliminary study on effect of Gegen Qinlian Decoction on enzyme activity, gene expression and methylation level of FASN in adipose tissue of rats with insulin resistance.
10.19540/j.cnki.cjcmm.20200901.401
- Author:
Yong-Qiang CHEN
1
;
Shu-Fang GONG
1
;
Xin HUANG
2
;
Zhi-Jun ZENG
3
;
Guo-Liang XU
3
;
Shu-Hong PENG
3
;
Wei-Feng ZHU
4
Author Information
1. Research Center for Differentiation and Development of Traditional Chinese Medicine Basic Theory,Jiangxi University of Traditional Chinese Medicine Nanchang 330004, China Jiangxi Province Key Laboratory of Traditional Chinese Medicine Etiopathogenisis Nanchang 330004, China College of Traditional Chinese Medicine, Jiangxi University of Traditional Chinese Medicine Nanchang 330004, China.
2. College of Traditional Chinese Medicine, Jiangxi University of Traditional Chinese Medicine Nanchang 330004, China.
3. Research Center for Differentiation and Development of Traditional Chinese Medicine Basic Theory,Jiangxi University of Traditional Chinese Medicine Nanchang 330004, China Jiangxi Province Key Laboratory of Traditional Chinese Medicine Etiopathogenisis Nanchang 330004, China.
4. Key Laboratory of Modern Preparation of Traditional Chinese Medicine, Ministry of Education, Jiangxi University of Traditional Chinese Medicine Nanchang 330004, China.
- Publication Type:Journal Article
- Keywords:
DNA methylation;
Gegen Qinlian Decoction;
fatty acid synthase;
insulin resistance;
transcription factor
- MeSH:
Adipose Tissue;
Animals;
Drugs, Chinese Herbal;
Fatty Acid Synthases/genetics*;
Gene Expression;
Insulin Resistance/genetics*;
Male;
Methylation;
Rats;
Rats, Sprague-Dawley
- From:
China Journal of Chinese Materia Medica
2021;46(2):398-405
- CountryChina
- Language:Chinese
-
Abstract:
To investigate the effect of Gegen Qinlian Decoction(GQD) on enzyme activity, gene expression and methylation level of fatty acid synthase(FASN) in adipose tissue from rats with insulin resistance induced by high-fat diet. The 60% fat-powered high-fat diet was continuously given to male SD rats to induce the insulin resistance model. Then, they were divided into five groups randomly and administrated by gavage every day for 16 weeks with following drugs respectively: 10 mL·kg~(-1)water for control group(C) and insulin resistance model control group(IR), 1.65 g·kg~(-1)GQD per day for low-dose group(GQDL), 4.95 g·kg~(-1)GQD per day for medium-dose group(GQDM), 14.85 g·kg~(-1)GQD per day for high-dose group(GQDH), and 5 mg·kg~(-1) rosiglitazone per day for rosiglitazone group(RGN). Epididymal adipose tissue was taken to determine enzyme activity of FASN by colorimetric method, mRNA expression level of Fasn by quantitative Real-time PCR(Q-PCR) and CpGs methylation level between +313 and +582 by bisulfite sequencing PCR(BSP). These results showed that Fasn expression was significantly lowered in IR model rats compared with the control rats(P<0.01). Enzymatic activity and CpGs methylation level of Fasn in IR group showed downward trends. Low and medium-dose GQD can increase enzyme activity of FASN(P<0.05). Moreover, low-dose GQD increased the total CpGs methylation level of Fasn fragment between +313 and +582 in insulin resistance rats(P<0.05). For GQDM group, the methylation frequency of CpGs at positions +506 and +508(P<0.01) as well as the methylation frequency of CpGs on the binding sites of transcription factorzinc finger protein 161(P<0.05) were significantly increased. The methylation frequency of CpG at +442 position was positively correlated with Fasn expression(P<0.01, r=0.735), and methylation frequencies of CpGs at +345 and +366 positions were positively associated to enzyme activity of FASN respectively(P<0.05, r=0.479; P<0.01, r=0.640). In conclusion, GQD can reverse enzyme activity of FASN and methylation level of Fasn in adipose tissue of insulin resistant rats, and CpG sites at positions +506 and +508 may be the targets of GQD. The methylation level of CpGs at + 345 and + 366 sites were possibly related to FASN activity, while methylation of CpG at + 442 site may be closely correlated with mRNA level of Fasn. In addition, GQD did not significantly change mRNA expression level of Fasn, but effectively reversed enzymatic activity, suggesting that GQD may regulate the post transcriptional expression of Fasn.
