Prevention of cyclosporine-induced nephrotoxicity with pentoxifylline.

Prevention of cyclosporine-induced nephrotoxicity with pentoxifylline.
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用己酮可可碱预防环孢素引起的肾毒性。

DOI:
10.3109/08860228909066950
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发表时间:
1989
期刊:
影响因子:
3
通讯作者:
D. Luke
D. Luke
中科院分区:
医学3区
文献类型:
--
作者:
L. J. Brunner;K. Vadiei;L. Iyer;D. Luke

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Although cyclosporine (CSA) is established in the prevention of allograft rejection, its use has been associated with dose-limiting toxicities, most notably to the kidney and liver. To date, the pathogenesis of the acute form of nephrotoxicity is unclear but may be related to inhibition of vasodilatory prostaglandins resulting in vasoconstriction and ischemia. The present study investigated the coadministration of CSA with a unique hemorheologic agent, pentoxifylline (PTX), in the murine model. A total of 48 rats were orally dosed with CSA 25 mg/kg for 10 days with either PTX 45 mg/kg i.p. or saline every 12 hr. Posttreatment renal function, assessed by creatinine (CCR) and inulin (CIN) clearances and renal electrolyte handling, was compared with baseline data and between groups. In an attempt to assess prostaglandin-mediated changes in enteral absorption, oral CSA pharmacokinetics with and without PTX were compared to the pharmacokinetics of similar groups (N = 8) administered i.v. CSA. Mean CIN of rats coadministered CSA and PTX (942 +/- 214 microliters/min/g KW) was similar to control rats 884 +/- 185 microliters/min/g KW); both were significantly greater than CSA alone (537 +/- 211 microliters/min/g KW; p less than .01). Likewise, percent of baseline CCR was significantly reduced in rats treated CSA (61 +/- 24%) compared to controls 113 +/- 41%) and rats coadministered PTX (117 +/- 75%; p less than .05). No differences in percent change from baseline electrolyte handling were observed among groups. Further, no differences in CSA pharmacokinetics with or without PTX were found.(ABSTRACT TRUNCATED AT 250 WORDS)
DOI: --
发表时间: 1988
影响因子: 0.9
作者:
Didlake,RH;Kim,EK;Grevel,J;Jarolimek,L;Kahan,BD
通讯作者: Kahan,BD
DOI: 10.1038/ki.1985.196
发表时间: 1985-11-01
影响因子: 19.6
作者:
MURRAY, BM;PALLER, MS;FERRIS, TF
通讯作者: FERRIS, TF