PRODUCTION OF PIPECOLIC ACID FROM INTESTINAL BACTERIA - PLASMA-LEVELSOF PIPECOLIC ACID IN PATIENTS WITH LIVER-CIRRHOSIS DECREASED AFTER ORAL KANAMYCIN ADMINISTRATION

Citation
Y. Matsuda et al., PRODUCTION OF PIPECOLIC ACID FROM INTESTINAL BACTERIA - PLASMA-LEVELSOF PIPECOLIC ACID IN PATIENTS WITH LIVER-CIRRHOSIS DECREASED AFTER ORAL KANAMYCIN ADMINISTRATION, HEPATOLOGY RESEARCH, 4(1), 1995, pp. 26-34
Citations number
20
Categorie Soggetti
Gastroenterology & Hepatology
Journal title
ISSN journal
13866346
Volume
4
Issue
1
Year of publication
1995
Pages
26 - 34
Database
ISI
SICI code
1386-6346(1995)4:1<26:POPAFI>2.0.ZU;2-8
Abstract
We analyzed the changes in plasma levels of pipecolic acid before and after the oral administration of kanamycin in patients with liver cirr hosis and investigated the relationship between plasma pipecolic acid and clinical laboratory tests. Twenty patients received oral kanamycin 1.5-3.0 g/day for 7-14 days. Plasma levels of pipecolic acid, which w ere determined by high-performance liquid chromatography after dansyl derivatization, significantly decreased following kanamycin administra tion (before 3.16 +/- 2.91 nmol/ml, after 2.37 +/- 2.48 nmol/ml; P = 0 .0002). In addition, plasma ammonia concentration also decreased, alth ough there were no significant changes in plasma lysine and the BCAA/A AA ratio. Plasma pipecolic acid correlated closely with plasma ammonia concentration (P < 0.0001), but not with other hepatic function tests such as ICGR(15), serum albumin, prothrombin time, the BCAA/AAA ratio , lysine and serum bilirubin. Plasma levels of pipecolic acid in patie nts with esophageal varices were significantly higher than those witho ut esophageal varices (P = 0.032). Plasma level of pipecolic acid in a patient with cirrhosis complicated with hepatic encephalopathy was lo wered after kanamycin administration concomitantly with the remission of hepatic encephalopathy. These results show that plasma pipecolic ac id is derived in part from intestinal bacteria and is correlated with the degrees of porto-systemic shunt volume.