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. 2001 Mar 2;5(Suppl 1):P081. doi: 10.1186/cc1148

Low dose pentoxifylline (PTX) reduces mortality in an animal model of acute hepatic and multi-organ failure

TM Rahman 1, HJF Hodgson 2
PMCID: PMC3333268

Introduction

Pentoxifylline inhibits, release of TNF-α, platelet aggregation and adherence of leukocytes to endothelium. Previous studies report increased mortality following its use.

Methods

AHF is induced by two intraperitoneal (i.p.) injections (500 mg/kg 8 hours apart) of TAA. Four groups were studied (n = 5). Group 1 received TAA only. Groups 2, 3, & 4 followed the protocol for Group 1, however, Groups 2 and 3 were pre-treated for 5 days with once daily high dose PTX (300 mg/kg i.p.) and low dose PTX (25 mg/kg i.p.), respectively. Whereas, Group 4, commenced PTX (25 mg/kg i.p.) post-TAA for 5 days. Mortality was determined at 96 hours in separate groups (n = 5).

Results

See Table.

Table 1.

Mortality
AST (iu/l) PT (s) Ammonia (μg/ml) Lactate (mmol/l) (%)
Hours 24 72 24 72 24 72 24 72 96

G1-TAA 1553 ± 343 4512 ± 501 26 ± 3 121 ± 12 58 ± 8 134 ± 12 2.6 ± 1.2 6.3 ± 0.4 75
G2-PTX 300 mg/kg 2065 ± 330 5221 ± 528 >121* >121 117 ± 34* 153 ± 13 3.9 ± 0.5 7.8 ± 0.6 100*
G3-PTX 25 mg/kg 1177 ± 177 2021 ± 43* 23 ± 4 101 ± 13 71.4 ± 9 70.2 ± 10* 3.5 ± 0.1 4.6 ± 0.2* 40*
G4-Post PTX 25 mg/kg 2161 ± 166 5014 ± 299 >121 >121 121 ± 8* 156 ± 12 4.7 ± 0.6* 7.4 ± 0.8 100*

*P < 0.05, mean ± SD.

Conclusion

Pre-treatment with low dose PTX reduces hepatic injury, multi-organ failure and mortality.


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