Effects of oxidative stress on the pharmacokinetics and hepatic metabolism of atazanavir in rats
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Kobuchi, S.
[1
]
Fukushima, K.
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Kobe Gakuin Univ, Fac Pharmaceut Sci, Dept Clin Pharmacokinet, Chuo Ku, Kobe, Hyogo, JapanKyoto Pharmaceut Univ, Dept Pharmacokinet, Yamashina Ku, Kyoto 6078412, Japan
Fukushima, K.
[2
]
Aoyama, H.
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Kyoto Pharmaceut Univ, Dept Pharmacokinet, Yamashina Ku, Kyoto 6078412, JapanKyoto Pharmaceut Univ, Dept Pharmacokinet, Yamashina Ku, Kyoto 6078412, Japan
Aoyama, H.
[1
]
Ito, Y.
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Kyoto Pharmaceut Univ, Dept Pharmacokinet, Yamashina Ku, Kyoto 6078412, JapanKyoto Pharmaceut Univ, Dept Pharmacokinet, Yamashina Ku, Kyoto 6078412, Japan
Ito, Y.
[1
]
Sugioka, N.
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Kobe Gakuin Univ, Fac Pharmaceut Sci, Dept Clin Pharmacokinet, Chuo Ku, Kobe, Hyogo, JapanKyoto Pharmaceut Univ, Dept Pharmacokinet, Yamashina Ku, Kyoto 6078412, Japan
Sugioka, N.
[2
]
Takada, K.
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Kyoto Pharmaceut Univ, Dept Pharmacokinet, Yamashina Ku, Kyoto 6078412, JapanKyoto Pharmaceut Univ, Dept Pharmacokinet, Yamashina Ku, Kyoto 6078412, Japan
Takada, K.
[1
]
机构:
[1] Kyoto Pharmaceut Univ, Dept Pharmacokinet, Yamashina Ku, Kyoto 6078412, Japan
[2] Kobe Gakuin Univ, Fac Pharmaceut Sci, Dept Clin Pharmacokinet, Chuo Ku, Kobe, Hyogo, Japan
drug metabolism;
cytochrome P450;
lipid peroxidation;
iron citrate complexes;
red blood cells;
LOW-DENSITY-LIPOPROTEIN;
FERRIC-NITRILOTRIACETATE;
LIPID-PEROXIDATION;
FE-NTA;
LIVER;
PLASMA;
IRON;
KIDNEY;
DRUGS;
CARCINOGENESIS;
D O I:
10.3109/10715762.2013.770149
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
We studied the effects of oxidative stress (OS) on the pharmacokinetics of atazanavir (ATV), particularly the distribution of ATV in the plasma and its metabolism in hepatic microsomes, using a rat model of ferric-nitrilotriacetate-induced OS (OS rats). The areas under the plasma concentration-time curves for intravenous bolus, oral, and intraportal administration of ATV in the OS rats were significantly greater than those in the control rats, whereas blood clearance of ATV after intravenous bolus injection in the OS rats (0.94. +/- 0.04 L/h/kg) was approximately half of that in the control rats (2.08 +/- 0.20 L/h/kg). Moreover, the intrinsic clearance (CLint), which is determined by in vitro metabolic studies using hepatic microsomal fractions of rats, was approximately 43% lower in the OS rats (0.489. +/- 0.017 mL/min/mg protein) than in the control rats (0.851. +/- 0.004 mL/min/mg protein). ATV concentrations in both the plasma-bound fraction and erythrocytes of the OS rats were significantly greater than those in the control rats. These results suggest that the hepatic metabolism of ATV may be reduced in patients under OS.