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Amphotericin B Lipid Complex or Amphotericin B Multiple-Dose Administration to Rabbits with Elevated Plasma Cholesterol Levels: Pharmacokinetics in Plasma and Blood Plasma Lipoprotein Levels Distribution in Tissues and Renal Toxicities

机译:对血浆胆固醇水平升高的家兔进行两性霉素B脂质复合物或两性霉素B多次给药:血浆和血液中的药代动力学血浆脂蛋白水平组织中的分布以及肾毒性

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摘要

The purpose of the present study was to determine if a relationship exists between the plasma cholesterol concentration, the severity of amphotericin B (AmpB)-induced renal toxicity, and the pharmacokinetics of AmpB in plasma in hypercholesterolemic rabbits administered multiple doses of amphotericin B (AmB) deoxycholate (Doc-AmB) and AmB lipid complex (ABLC). After 7 days of administration of a cholesterol-enriched diet (0.50% [wt/vol]) or a regular rabbit diet, each rabbit was administered a single intravenous bolus of Doc-AmB (n = 8) or ABLC (n = 10) (1.0 mg/kg of body weight) daily for 7 consecutive days (a total of eight doses). Blood samples were obtained daily before and 24 h after the administration of each dose and serially thereafter following the administration of the last dose for the assessment of pharmacokinetics in plasma, kidney toxicity, plasma lipoprotein levels, and drug distribution in tissue. The pharmacokinetics of AmB in blood following the administration of ABLC were also determined in rabbits fed cholesterol-enriched and regular diets (n = 3 each group). Before drug treatment, cholesterol-fed rabbits demonstrated marked increases in total, low-density lipoprotein (LDL), and triglyceride-rich lipoprotein (TRL) cholesterol levels in plasma compared with the levels in rabbits on a regular diet. No significant differences in total plasma triglyceride levels were observed. Significant increases in plasma creatinine levels were observed in rabbits fed a cholesterol-enriched diet (P < 0.05) and rabbits fed a regular diet (P < 0.05) when administered AmB. However, the magnitude of this increase was twofold greater in rabbits fed a regular diet than in rabbits fed a cholesterol-enriched diet. An increase in plasma creatinine levels was observed only in rabbits on a cholesterol-enriched diet administered ABLC. The pharmacokinetics of AmB were significantly altered in rabbits on a cholesterol-enriched diet administered Doc-AmB or ABLC compared to those in rabbits on a regular diet administered each of these compounds. The pharmacokinetics of AmB in blood were significantly different following ABLC administration but not following Doc-AmB administration in both rabbits fed cholesterol-enriched diets and rabbits fed regular diets compared to their corresponding pharmacokinetics in plasma. An increased percentage of AmB was recovered in the TRL fraction when Doc-AmB was administered to rabbits fed a cholesterol-enriched diet than when it was administered to rabbits fed a regular diet. Furthermore, an increased percentage of AmB was recovered in the LDL and TRL fractions when ABLC was administered to rabbits fed a cholesterol-enriched diet rabbits fed a regular diet. These findings suggest that an increase in plasma cholesterol levels modifies the pharmacokinetics of AmB and renal toxicity following the administration of multiple intravenous doses of Doc-AmB and ABLC.
机译:本研究的目的是确定血浆胆固醇浓度,两性霉素B(AmpB)引起的肾脏毒性的严重程度以及多剂量两性霉素B(AmB)的高胆固醇血症兔血浆中AmpB的药代动力学之间是否存在关系)脱氧胆酸盐(Doc-AmB)和AmB脂质复合物(ABLC)。在给予富含胆固醇的饮食(0.50%[wt / vol])或常规兔子饮食7天后,每只兔子都被单次静脉推注Doc-AmB(n = 8)或ABLC(n = 10)连续7天每天(1.0毫克/千克体重)(共八剂)。每天在每次剂量给药之前和之后24小时获取血样,然后在最后一次给药之后连续获取血样,以评估血浆中的药代动力学,肾脏毒性,血浆脂蛋白水平以及组织中的药物分布。还测定了饲喂富含胆固醇和常规饮食(每组n = 3)的兔子中ABLC给药后血液中AmB的药代动力学。在进行药物治疗之前,胆固醇喂养的兔子血浆中的总胆固醇,低密度脂蛋白(LDL)和富含甘油三酸酯的脂蛋白(TRL)胆固醇水平明显高于常规饮食中的兔子水平。没有观察到总血浆甘油三酯水平的显着差异。饲喂高胆固醇饮食的兔子(P <0.05)和常规饮食(P <0.05)的兔子在服用AmB后观察到血浆肌酐水平显着增加。然而,这种增加的幅度在喂食常规饮食的兔子中要比喂食富含胆固醇的饮食的兔子大两倍。仅在接受了ABLC的高胆固醇饮食的兔子中观察到血浆肌酐水平的增加。与在常规饮食中施用这些化合物的兔子相比,在使用富含胆固醇的饮食中施用Doc-AmB或ABLC的兔子中AmB的药代动力学显着改变。与血浆中相应的药代动力学相比,ABLC给药后,AmB在血液中的药代动力学显着不同,但在Doc-AmB给药后,与饲喂高胆固醇饮食的兔子和常规饮食相比,其血浆中的药代动力学差异显着。与饲喂普通饮食的兔子服用Doc-AmB相比,将Doc-AmB饲喂给兔子的TRL分数增加了。此外,当ABLC给予饲喂高胆固醇饮食的兔子喂食常规饮食时,在LDL和TRL馏分中回收的AmB百分比增加。这些发现表明,在多次静脉给药Doc-AmB和ABLC后,血浆胆固醇水平的升高改变了AmB的药代动力学和肾毒性。

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