Variable effects of short chain fatty acids and lactic acid in inducing intestinal mucosal injury in newborn rats

被引:53
作者
Lin, J
Nafday, SM
Chauvin, SN
Magid, MS
Pabbatireddy, S
Holzman, IR
Babyatsky, MW
机构
[1] CUNY Mt Sinai Sch Med, Div Newborn Med, Jack & Lucy Clark Dept Pediat, New York, NY 10029 USA
[2] CUNY Mt Sinai Sch Med, Dept Pediat, New York, NY 10029 USA
[3] CUNY Mt Sinai Sch Med, Dept Pathol, New York, NY 10029 USA
[4] CUNY Mt Sinai Sch Med, Dept Med, New York, NY 10029 USA
关键词
short chain fatty acids; lactic acid; enterocolitis; necrotizing;
D O I
10.1097/00005176-200210000-00016
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background: Short chain fatty acids and lactic acid are colonic bacterial fermentation products. Methods: To evaluate the effects of these organic acids on the intestinal mucosa, a total of 72 newborn Sprague-Dawley rats (10 days old) were studied. A 3.5F catheter was inserted per rectum 4.0 cm deep into the proximal colon for organic acid administration at a volume of 0.1 ml/10 g body weight. The pH of organic acid solutions and normal saline was adjusted to 4.0. Group I (n = 10) received normal saline as a control. Group 2 (n = 11) received 150 mM acetic acid. Group 3 (n = 11) received 300 mM acetic acid. Group 4 (n = 10) received 150 mM butyric acid. Group 5 (n = 11) received 300 mM butyric acid. Group 6 (n = 7) received 150 mM lactic acid, and group 7 (n = 12) received 300 mM lactic acid. Animals were killed 24 hours after colonic installation of test solutions. Results: Both 300 mM acetic acid and 300 mM butyric acid were associated with impaired weight gain, increased colon wet weight, and increased histologic injury scores in the colon and distal ileum (P < 0.05, analysis of variance). Both 150 mM acetic acid and butyric acid at 150 mmol/L induced minimal injury in the colon and distal ileum. Neither 150 mM nor 300 mM lactic acid induced any identifiable gross or microscopic intestinal mucosal injury. Conclusion: Luminal short chain fatty acids can induce dose-dependent intestinal mucosal injury in newborn rats, resembling the pathology seen in neonatal necrotizing enterocolitis. Overproduction/accumulation of short chain fatty acids, but not lactic acid, in the proximal colon and/or distal ileum may play a role in the pathogenesis of necrotizing enterocolitis in premature infants.
引用
收藏
页码:545 / 550
页数:6
相关论文
共 38 条
[1]  
ARGENZIO RA, 1991, DIGEST DIS SCI, V36, P1495
[2]   Apoptosis cascade proteins are regulated in vivo by high intracolonic butyrate concentration: Correlation with colon cancer inhibition [J].
Avivi-Green, C ;
Polak-Charcon, S ;
Madar, Z ;
Schwartz, B .
ONCOLOGY RESEARCH, 2000, 12 (02) :83-95
[3]   PATHOLOGY OF NEONATAL NECROTIZING ENTEROCOLITIS - A 10-YEAR EXPERIENCE [J].
BALLANCE, WA ;
DAHMS, BB ;
SHENKER, N ;
KLIEGMAN, RM .
JOURNAL OF PEDIATRICS, 1990, 117 (01) :S6-S13
[4]  
Bianchi-Salvadori B, 2001, MICROBIOLOGICA, V24, P23
[5]   FATE OF SOLUBLE CARBOHYDRATE IN COLON OF RATS AND MAN [J].
BOND, JH ;
LEVITT, MD .
JOURNAL OF CLINICAL INVESTIGATION, 1976, 57 (05) :1158-1164
[6]   Clostridial pathogenicity in experimental necrotising enterocolitis in gnotobiotic quails and protective role of bifidobacteria [J].
Butel, MJ ;
Roland, N ;
Hibert, A ;
Popot, F ;
Favre, A ;
Tessedre, AC ;
Bensaada, M ;
Rimbault, A ;
Szylit, O .
JOURNAL OF MEDICAL MICROBIOLOGY, 1998, 47 (05) :391-399
[7]   New concepts in necrotizing enterocolitis [J].
Caplan, MS ;
Jilling, T .
CURRENT OPINION IN PEDIATRICS, 2001, 13 (02) :111-115
[8]   Bifidobacterial supplementation reduces the incidence of necrotizing enterocolitis in a neonatal rat model [J].
Caplan, MS ;
Miller-Catchpole, R ;
Kaup, S ;
Russell, T ;
Lickerman, M ;
Amer, M ;
Xiao, Y ;
Thomson, R .
GASTROENTEROLOGY, 1999, 117 (03) :577-583
[9]   BREATH HYDROGEN EXCRETION AS A SCREENING-TEST FOR THE EARLY DIAGNOSIS OF NECROTIZING ENTEROCOLITIS [J].
CHEU, HW ;
BROWN, DR ;
ROWE, MI .
AMERICAN JOURNAL OF DISEASES OF CHILDREN, 1989, 143 (02) :156-159
[10]   NECROTIZING ENTEROCOLITIS - INTRALUMINAL BIOCHEMISTRY IN HUMAN NEONATES AND A RABBIT MODEL [J].
CLARK, DA ;
THOMPSON, JE ;
WEINER, LB ;
MCMILLAN, JA ;
SCHNEIDER, AJ ;
ROKAHR, JE .
PEDIATRIC RESEARCH, 1985, 19 (09) :919-921