High intracolonic acetaldehyde values produced by a bacteriocolonic pathway for ethanol oxidation in piglets

被引:73
作者
Jokelainen, K
MatysiakBudnik, T
Makisalo, H
Hockerstedt, K
Salaspuro, M
机构
[1] UNIV HELSINKI,CENT HOSP,ALCOHOL DIS RES UNIT,HELSINKI,FINLAND
[2] UNIV HELSINKI,CENT HOSP,DEPT SURG 4,HELSINKI,FINLAND
关键词
alcohol; ethanol; acetaldehyde; colonic bacteria; ethanol toxicity;
D O I
10.1136/gut.39.1.100
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background-Human colonic contents and many colonic microbes produce considerable amounts of acetaldehyde from ethanol in vitro. Aims-To examine in piglets if acetaldehyde is produced in the colon also in vivo, and if so, what is the fate of intracolonically formed acetaldehyde. Animals-Seventeen native, non-fasted female piglets (20-25 kg) were used. Methods-Six piglets received either 1.5 g/kg bw or 2.5 g/kg bw of ethanol intravenously. In seven piglets, 0.7 g or 1.75 g of ethanol/kg bw was administered intravenously, followed by a subsequent intragastric ethanol infusion of 1.8 g/kg bw and 4.5 g/kg bw, respectively. The samples of colonic contents for the assessment of ethanol and acetaldehyde concentrations were obtained up to seven hours, In four additional piglets, the intracolonic values of ethanol, acetaldehyde, and acetate were observed for 60 minutes after an intracolonic infusion of acetaldehyde solution. Results-A raised intracolonic, endogenous acetaldehyde concentration (mean (SEM); 36 (9) mu M) was found in all piglets before ethanol infusion. After the infusion of ethanol, intracolonic ethanol and acetaldehyde values increased in parallel, reaching the peak values 57 (4) mM of ethanol and 271 (20) mu M of acetaldehyde in the group that received the highest dose of ethanol. A positive correlation (r=0.45; p<0.001) was found between intracolonic ethanol and acetaldehyde values. Acetaldehyde administered intracolonically was mainly metabolised to acetate but also to ethanol in the colon, Conclusions-Significant endogenous intracolonic acetaldehyde values can be found in the normal porcine colon. Furthermore, our results suggest the existence of a bacteriocolonic pathway for ethanol oxidation. Increased amounts of acetaldehyde are formed intracolonically from ingested ethanol by this pathway.
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页码:100 / 104
页数:5
相关论文
共 48 条
  • [31] MINUK GY, 1994, HEPATOLOGY, V20, pA317
  • [32] THE 2 ALCOHOL DEHYDROGENASES OF ZYMOMONAS-MOBILIS - PURIFICATION BY DIFFERENTIAL DYE LIGAND CHROMATOGRAPHY, MOLECULAR CHARACTERIZATION AND PHYSIOLOGICAL ROLES
    NEALE, AD
    SCOPES, RK
    KELLY, JM
    WETTENHALL, REH
    [J]. EUROPEAN JOURNAL OF BIOCHEMISTRY, 1986, 154 (01): : 119 - 124
  • [33] PACE DM, 1960, CANCER RES, V20, P868
  • [34] POST-JEJUNOILEAL-BYPASS HEPATIC DISEASE - ITS SIMILARITY TO ALCOHOLIC HEPATIC DISEASE
    PETERS, RL
    GAY, T
    REYNOLDS, TB
    [J]. AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1975, 63 (03) : 318 - 331
  • [35] PROSPECTIVE-STUDY OF ALCOHOL-CONSUMPTION AND CANCER
    POLLACK, ES
    NOMURA, AMY
    HEILBRUN, LK
    STEMMERMANN, GN
    GREEN, SB
    [J]. NEW ENGLAND JOURNAL OF MEDICINE, 1984, 310 (10) : 617 - 621
  • [36] MOLECULAR CHARACTERIZATION OF MICROBIAL ALCOHOL DEHYDROGENASES
    REID, MF
    FEWSON, CA
    [J]. CRITICAL REVIEWS IN MICROBIOLOGY, 1994, 20 (01) : 13 - 56
  • [37] CHARACTERISTICS OF HELICOBACTER-PYLORI ALCOHOL-DEHYDROGENASE
    SALMELA, KS
    ROINE, RP
    KOIVISTO, T
    HOOKNIKANNE, J
    KOSUNEN, TU
    SALASPURO, M
    [J]. GASTROENTEROLOGY, 1993, 105 (02) : 325 - 330
  • [38] ALCOHOLIC CARDIOMYOPATHY .2. INHIBITION OF CARDIAC MICROSOMAL PROTEIN-SYNTHESIS BY ACETALDEHYDE
    SCHREIBER, SS
    ORATZ, M
    ROTHSCHILD, MA
    REFF, F
    EVANS, C
    [J]. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY, 1974, 6 (02) : 207 - 213
  • [39] POSSIBLE ROLE OF ACETALDEHYDE IN ETHANOL-RELATED RECTAL COCARCINOGENESIS IN THE RAT
    SEITZ, HK
    SIMANOWSKI, UA
    GARZON, FT
    RIDEOUT, JM
    PETERS, TJ
    KOCH, A
    BERGER, MR
    EINECKE, H
    MAIWALD, M
    [J]. GASTROENTEROLOGY, 1990, 98 (02) : 406 - 413
  • [40] SEITZ HK, 1984, GASTROENTEROLOGY, V86, P886