Abstract
Pharmacokinetic and pharmacological studies were performed to compare the antipyretic
effects of salicin (SL), saligenin (SG, an aglycone of SL) and salicylic acid (SA,
an active metabolite of SL) in rats. When SL was administered orally to rats, SA appeared
slowly in the plasma and levels increased gradually, in contrast to the rapid appearance
observed after oral administration of sodium salicylate (SANa) or SG. Orally administered
SL did not affect the rectal temperatures of afebrile rats at a dose of 5 mmol/kg;
at this dose, SANa and SG lowered body temperature significantly. However, it significantly
reduced yeast-induced fever, producing a normal body temperature, and completely prevented
fever when administered simultaneously with yeast. SL did not induce gastric lesions
even at a dose of 5 mmol/kg; conversely, SANa and SG induced severe gastric lesions
in a dose-dependent manner at 1, 2.5 and 5 mmol/kg. Poor absorption of SL and rapid
absorption of SA and SG were confirmed in an in vivo system, as well as in an in vitro system using everted rat jejunal sacs. Only small amounts of SA and SG were detected
in the intestinal tracts of rats 1 h after oral administration, whereas more than
50 % of an SL dose was recovered as SL and SG from the intestinal tracts 1 h after
treatment and 15.8 % of the dose was still present as SG 4 h after administration.
When given to germ-free rats, 19.8 % of the SL dose was recovered intact, mainly from
the cecum, and no SG was detected even at 4 h after treatment. These results indicate
that SL is a prodrug which is gradually transported to the lower part of the intestine,
hydrolyzed to SG by intestinal bacteria, and converted to SA after absorption. It
thus produces an antipyretic action without causing gastric injury.
Abbreviations
SL:salicin
SG:saligenin
SA:salicylic acid
SANa:sodium salicylate
NSAIDs:non-steroidal anti-inflammatory drugs
Key words
Salicin - salicylic acid - saligenin - antipyretic - intestinal bacteria - gastric
lesion - prodrug
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Dr. T. Akao
Faculty of Pharmaceutical Sciences
Toyama Medical and Pharmaceutical University
2630 Sugitani
Toyama 930-0194
Japan
Email: ta0113@ms.toyama-mpu.ac.jp
Fax: +81(076)434-4656