2016
DOI: 10.4103/0973-1296.186340
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Expression of cytochrome P450s in the liver of rats administered with Socheongryong-tang, a traditional herbal formula

Abstract: Objective:The purpose of this study was to investigate the potential influences of Socheongryong-tang (SCRT) on the messenger ribonucleic acid (mRNA) and protein expression of cytochrome P450 (CYP450) in vivo.Materials and Methods:SCRT was orally administered to either male or female Sprague-Dawley rats once daily at doses of 0, 1000, 2000, or 5000 mg/kg/day for 13 weeks. The mRNA expression of CYP450s (CYP1A1, 1A2, 2B1/2, 2C11, 2E1, 3A1, 3A2, and 4A1) in liver tissues was measured by reverse transcription pol… Show more

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Cited by 7 publications
(3 citation statements)
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“…HCC is characterized by uncontrolled cell proliferation. 49 Formulas such as son-you-yin 12 and so-cheong-ryong-tang 50 as well as herbs including Danshen 51 and Huangyaozi 52 significantly inhibit cell proliferation and tumor growth in HCC. The compounds isolated from herbs Raddeanin A, 53 and Ardipusilloside-I 54 also showed anti-proliferative effects in HCC cells.…”
Section: History Of Tcm For Hcc Prevention and Therapymentioning
confidence: 99%
“…HCC is characterized by uncontrolled cell proliferation. 49 Formulas such as son-you-yin 12 and so-cheong-ryong-tang 50 as well as herbs including Danshen 51 and Huangyaozi 52 significantly inhibit cell proliferation and tumor growth in HCC. The compounds isolated from herbs Raddeanin A, 53 and Ardipusilloside-I 54 also showed anti-proliferative effects in HCC cells.…”
Section: History Of Tcm For Hcc Prevention and Therapymentioning
confidence: 99%
“…38 CYP induction by drugs is one of the major side-effects of drug administration. 39,40 The activity of CYP genes also is an indication of functionality of hepatocytes. The major gene in rats for CYP450 activity is CYP1A1.…”
Section: Resultsmentioning
confidence: 99%
“…Certain gene polymorphisms in the CYP450 superfamily may cause intrinsic drug resistance by affecting protein function. 9,30 In Phase II, the drug binds glutathione, glucuronic acid, or sulfate via glutathione S -transferase (GST), UDP-glucuronosyl transferase, and sulfase catalysis, respectively and drug toxicity is attenuated. 9 In Phase III, metabolites are generated by efflux pumps such as P-gp and MRP family members.…”
Section: Increased Drug Metabolismmentioning
confidence: 99%