Effects of intestinal mucosal blood flow and motility on intestinal mucosa

被引:0
|
作者
Yan-Bin Wang
机构
关键词
Traumatic brain injury; Intestinal mucosa barrier; Stress; Intestinal mucosa blood flow; Intestinal motility;
D O I
暂无
中图分类号
R651.15 []; R574 [肠疾病];
学科分类号
1002 ; 100201 ; 100210 ;
摘要
AIM:To investigate the role of intestinal mucosal blood flow(IMBF) and motility in the damage of intestinal mucosal barrier in rats with traumatic brain injury.METHODS:Sixty-four healthy male Wistar rats were divided randomly into two groups:traumatic brain injury(TBI) group(n = 32),rats with traumatic brain injury;and control group(n = 32),rats with sham-operation.Each group was divided into four subgroups(n = 8) as 6,12,24 and 48 h after operation.Intestinal motility was measured by the propulsion ratio of a semi-solid colored marker(carbon-ink).IMBF was measured with the laser-Doppler technique.Endotoxin and D-xylose levels in plasma were measured to evaluate the change of intestinal mucosal barrier function following TBI.RESULTS:The level of endotoxin was significantly higher in TBI group than in the control group at each time point(0.382 ± 0.014 EU/mL vs 0.102 ± 0.007 EU/mL,0.466 ± 0.018 EU/mL vs 0.114 ± 0.021 EU/mL,0.478 ± 0.029 EU/mL vs 0.112 ± 0.018 EU/mL and 0.412 ± 0.036 EU/mL vs 0.108 ± 0.011 EU/mL,P < 0.05).D-xylose concentrations in plasma in TBI group were significantly higher than in the control group(6.68 ± 2.37 mmol/L vs 3.66 ±1.07 mmol/L,8.51 ± 2.69 mmol /L vs 3.15 ± 0.95 mmol/L,11.68 ± 3.24 mmol/L vs 3.78 ± 1.12 mmol/L and 10.23 ± 2.83 mmol/L vs 3.34 ± 1.23 mmol/L,P < 0.05).The IMBF in TBI group was significantly lower than that in the control group(38.5 ± 2.8 PU vs 45.6 ± 4.6 PU,25.2 ± 3.1 PU vs 48.2 ± 5.3 PU,21.5 ± 2.7 PU vs 44.9 ± 2.8 PU,29.4 ± 3.8 PU vs 46.7 ± 3.2 PU)(P < 0.05).Significant decelerations of intestinal propulsion ratio in TBI groups were found compared with the control group(0.48% ± 0.06% vs 0.62% ± 0.03%,0.37% ± 0.05% vs 0.64% ± 0.01%,0.39% ± 0.07% vs 0.63% ± 0.05% and 0.46% ± 0.03% vs 0.65% ± 0.02%)(P < 0.05).CONCLUSION:The intestinal mucosal permeability is increased obviously in TBI rats.Decrease of intestinal motility and IMBF occur early in TBI,both are important pathogenic factors for stress-related damage of the intestinal mucosal barrier in TBI.
引用
收藏
页码:657 / 661
页数:5
相关论文
共 50 条
  • [41] RELATION BETWEEN INTESTINAL MOTILITY AND MESENTERIC BLOOD-FLOW IN THE CONSCIOUS DOG
    FIORAMONTI, J
    BUENO, L
    AMERICAN JOURNAL OF PHYSIOLOGY, 1984, 246 (02): : G108 - G113
  • [42] EFFECTS OF ETHANOL OF INTESTINAL MOTILITY IN MAN
    ROBLES, EA
    SCHUSTER, MM
    MEZEY, E
    HALSTED, CH
    GASTROENTEROLOGY, 1972, 62 (04) : 799 - &
  • [43] Effects of serotonin on intestinal secretion and motility
    Spiller, RC
    CURRENT OPINION IN GASTROENTEROLOGY, 2001, 17 (02) : 99 - 103
  • [44] EFFECTS OF EXPERIMENTAL HYPERTHYROIDISM ON INTESTINAL MOTILITY
    KARAUS, M
    ENCK, P
    GRUSSENDORF, M
    WIENBECK, M
    ERCKENBRECHT, JF
    HEPATO-GASTROENTEROLOGY, 1988, 35 (04) : 199 - 200
  • [45] INTESTINAL MUSCLE AND MUCOSAL BLOOD-FLOW DURING DIRECT SYMPATHETIC STIMULATION
    BOHLEN, HG
    HENRICH, H
    GORE, RW
    JOHNSON, PC
    AMERICAN JOURNAL OF PHYSIOLOGY, 1978, 235 (01): : H40 - H45
  • [46] MOTILITY EFFECTS OF INTESTINAL ANAPHYLAXIS IN THE RAT
    SCOTT, RB
    DIAMANT, SC
    GALL, DG
    AMERICAN JOURNAL OF PHYSIOLOGY, 1988, 255 (04): : G505 - G511
  • [47] ESTIMATION OF CANINE INTESTINAL MUCOSAL BLOOD-FLOW BY LASER DOPPLER VELOCIMETRY
    FELD, AD
    FONDACARO, JD
    HOLLOWAY, GA
    JACOBSON, ED
    CLINICAL RESEARCH, 1981, 29 (04): : A758 - A758
  • [48] MESENTERIC HEMODYNAMIC EFFECTS OF INTESTINAL MOTILITY
    KACHELHOFFER, J
    POUSSE, A
    HOHMATTER, D
    GRENIER, JF
    EUROPEAN SURGICAL RESEARCH, 1976, 8 : 60 - 61
  • [49] THE EFFECTS OF ISCHEMIA AND REPERFUSION ON INTESTINAL MOTILITY
    HEBRA, A
    BROWN, MF
    MCGEEHIN, K
    BROUSSARD, D
    ROSS, AJ
    JOURNAL OF PEDIATRIC SURGERY, 1993, 28 (03) : 362 - 366
  • [50] EFFECTS OF VAGOTOMY ON INTESTINAL MOTILITY IN DOGS
    WINGATE, DL
    REVERDIN, N
    HUTTON, M
    LING, A
    CHRISTOFIDES, N
    ADRIAN, TE
    BLOOM, SR
    RITCHIE, HD
    GASTROENTEROLOGIE CLINIQUE ET BIOLOGIQUE, 1979, 3 (01): : 90 - 90