Kuendee Natthaporn, Naladta Alisa, Kulsirirat Thitianan, Yimsoo Thunyatorn, Yingmema Werayut, Pansuksan Kanoktip, Sathirakul Korbtham, Sukprasert Sophida
Faculty of Veterinary Medicine, Rajamangala University of Technology Tawan-ok, Chonburi 20110, Thailand.
Department of Biochemistry, Faculty of Science, Khon Kaen University, Khon Kaen 40002, Thailand.
Pharmaceuticals (Basel). 2023 Feb 3;16(2):237. doi: 10.3390/ph16020237.
(Craib) A. Schmitz (LS) has been traditionally used as a medicinal herb by folk healers in Thailand with rare evidence-based support. Hepatic cytochrome P450s (CYPs450) are well known as the drug-metabolizing enzymes that catalyze all drugs and toxicants. In this study, we investigated the mRNA levels of six clinically important CYPs450, i.e., CYP1A2, 3A2, 2C11, 2D1, 2D2, and 2E1, in rats given LS extracts. Seventy Wistar rats were randomized into seven groups (n = 10). Each group was given LS stem ethanol (SE) and leaf water (LW) extracts orally at doses of 300, 2000, and 5000 mg/kg body weight (mg/kg.bw) for twenty-eight consecutive days. After treatment, the expression of CYPs450 genes was measured using quantitative real-time PCR. The results revealed that SE and LW, which contained quercetin and gallic acid, promoted the upregulation of all CYPs450. Almost all CYPs450 genes were downregulated in all male LW-treated rats but upregulated in female-treated groups, suggesting that CYP gene expressions in LS-treated rats were influenced by gender. Moderate and high doses of the LS extracts had a tendency to induce six CYP450s' transcription levels in both rat genders. CYP2E1 gene showed a unique expression level in male rats receiving SE at a dose of 2000 mg/kg.bw, whereas a low dose of 300 mg/kg.bw was found in the LW-treated female group. As a result, our findings suggest that different doses of LS extracts can moderate the varying mRNA expression of clinically relevant CYP genes. In this study, we provide information about CYP induction and inhibition in vivo, which could be a desirable condition for furthering the practical use of LS extracts in humans.
(克莱布)A.施密茨(LS)传统上一直被泰国民间治疗师用作草药,但缺乏基于证据的支持。肝细胞色素P450(CYPs450)作为催化所有药物和毒物的药物代谢酶而广为人知。在本研究中,我们调查了给予LS提取物的大鼠中六种临床重要的CYPs450,即CYP1A2、3A2、2C11、2D1、2D2和2E1的mRNA水平。70只Wistar大鼠被随机分为七组(n = 10)。每组大鼠连续28天口服给予300、2000和5000毫克/千克体重(mg/kg.bw)剂量的LS茎乙醇(SE)提取物和叶水(LW)提取物。治疗后,使用定量实时PCR测量CYPs450基因的表达。结果显示,含有槲皮素和没食子酸的SE和LW促进了所有CYPs450的上调。几乎所有CYPs450基因在所有接受LW治疗的雄性大鼠中均下调,但在接受治疗的雌性组中上调,这表明LS治疗大鼠中CYP基因的表达受性别影响。中高剂量的LS提取物倾向于诱导两种性别的大鼠中六种CYP450的转录水平。CYP2E1基因在接受2000 mg/kg.bw剂量SE的雄性大鼠中表现出独特的表达水平,而在接受LW治疗的雌性组中发现低剂量为300 mg/kg.bw。因此,我们的研究结果表明,不同剂量的LS提取物可以调节临床相关CYP基因的不同mRNA表达。在本研究中,我们提供了体内CYP诱导和抑制的信息,这可能是进一步推动LS提取物在人类中实际应用的理想条件。