Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5905770 | Gene | 2014 | 6 Pages |
Abstract
Epigallocatechin gallate (EGCG), the major active component of the green tea, has recently been found to inhibit 3-hydroxy-3-methylglutaryl-CoA reductase (HMGCoAR) activity in vitro and to modulate lipogenesis in vivo. In this study we have evaluated the effects of short-term in vivo exposure to EGCG (6 μg gâ 1 BW or 9 μg gâ 1 BW) on hepatic HMGCoAR gene expression of goldfish (Carassius auratus). We initially characterized a partial sequence of goldfish HMGCoAR suggesting that the obtained fragment shares high similarity (> 92%) with other fish HMGCoAR sequences. Further, the HMGCoAR transcript was detected in all goldfish tissues (except muscle) but primarily in liver, brain and gonads; on the contrary, low expression levels were found in intestine, heart, gill, and kidney. Both EGCG doses significantly decreased hepatic HMGCoAR mRNA levels 180 min post-injection. HMGCoAR was also significantly down-regulated at 90 min after injection in fish treated with the highest dose of EGCG. Our results demonstrate that hepatic HMGCoAR gene expression is acutely responsive to short-term EGCG exposure in goldfish. This finding suggests a potential role of EGCG in transcriptional regulation of the rate-limiting enzyme in cholesterol synthesis.
Keywords
SREBPSterol regulatory element-binding transcription factor 1CYP7A1SSDORFHMGCoARNADPHEGCGCarassius auratusppmRT-PCRABCA1MS-222SREBF1LXR3-hydroxy-3-methylglutaryl-CoA reductaseATP-binding cassette transporter A1Real-time PCRExpression patternepigallocatechin gallatepart per millionstandard error of the meansterol-sensing domainopen reading frameSEMnicotinamide adenine dinucleotide phosphatebody weightsterol regulatory element binding proteinliver X receptor
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Authors
Paolo Cocci, Gilberto Mosconi, Francesco Alessandro Palermo,