β-lonone has been reported to induce the cytochrome P450 (P450) 2B1 in rats. In this study, the effects of and an isomer, α-lonone, on liver P450 1A and 2B experssion in Sprague Dawley rats were investigated. Subctaneous administration of α-and �...
http://chineseinput.net/에서 pinyin(병음)방식으로 중국어를 변환할 수 있습니다.
변환된 중국어를 복사하여 사용하시면 됩니다.
https://www.riss.kr/link?id=A30068489
Jeong, Hye Gwang (College of Pharmacy, of Chosun University) ; Chun, Young-Jin (College of Pharmacy, Chung-Ang University) ; Yun, Chul-Ho (Department of Genetic Engineering, Pai-Chai University) ; Moon, Chang-Kiu (College of Pharmacy, Seoul National University) ; Lee, Hye-Sook (College of Pharmacy, Wonkwang University) ; Han, Sang Seop (Toxicology Research Center, Korea Research Institute of Chemical Technology) ; Lee, Eung-Seok (College of Pharmacy, Yeungnam University) ; Jeong, Tae Cheon (College of Pharmacy, Yeungnam University)
2002
English
518.000
학술저널
102-106(5쪽)
※ KISS의 원문 서비스 중단에 따라, 학술지명을 클릭하여 [복사/대출] 서비스를 이용해 주시기 바랍니다.
0
상세조회0
다운로드다국어 초록 (Multilingual Abstract)
β-lonone has been reported to induce the cytochrome P450 (P450) 2B1 in rats. In this study, the effects of and an isomer, α-lonone, on liver P450 1A and 2B experssion in Sprague Dawley rats were investigated. Subctaneous administration of α-and �...
β-lonone has been reported to induce the cytochrome P450 (P450) 2B1 in rats. In this study, the effects of and an isomer, α-lonone, on liver P450 1A and 2B experssion in Sprague Dawley rats were investigated. Subctaneous administration of α-and β-ionone 72 and 48hr prior to sacrificing the animals induced the liver microsomal P450 1A and 2B proteins. P450 2B1 induction was associated with the accumulation of its corresponding mRNA. Induction by β-ionone was much higher than that by α-ionone in both the mRNA and protein levels. When the route of administration was compared. P450 2B was induced more strongly after oral administration compared to that after subcutaneous injection. A single oral dose of 100, 300 and 600 mg/kg of α- and β-ionone for 24 h induced P450 2B-1selective pantoxyresorufin O-depentylase activity comparably in a dose-dependent manner. In addition, α- and β-ionone might be potent P450 2B1 inducers in rats, and that both ionones may be useful for examining the role of metabolic activation in chemical-induced toxicity where metabolic activation is required.
Physicochemical Characterization and Evaluation of Buccal Adhesive Tablets Containing Omeprazole
Terfenadine-β-Cyclodextrin Inclusion Complex with Antihistaminic Activity Enhancement