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大鼠小肠和大肠中甘露醇通透性的机制及部位

Mechanisms and sites of mannitol permeability of small and large intestine in the rat.

作者信息

Krugliak P, Hollander D, Schlaepfer C C, Nguyen H, Ma T Y

机构信息

Department of Medicine, University of California, Irvine 92717.

出版信息

Dig Dis Sci. 1994 Apr;39(4):796-801. doi: 10.1007/BF02087426.

Abstract

Mannitol is commonly used as an intestinal permeability probe, yet the mechanisms of its penetration of the intestinal barrier are not entirely clear. Therefore, we studied mannitol's permeability of different segments of the intestine and studied the kinetics and influence of intraluminal factors on mannitol permeability in vivo in perfused intestinal segments of rats. There was linear relationship between permeability rate of mannitol and its luminal concentration (y = 7.2x + 1.7; r = 0.98), indicating that passive diffusion is involved in mannitol's permeability. Increased luminal fluid osmolarity from 0.3 to 0.6 osmol/liter resulted in decreased net water flux with a corresponding decrease in mannitol permeability in both jejunum and colon (P < 0.01), indicating the prominent influence of solvent drag on net mannitol permeability. The relationship between mannitol permeability and water absorption at different osmolarities was linear in the jejunum and colon. At luminal osmolarity of 0.3 osmol/liter, 34.6% of mannitol permeability was mediated by passive diffusion and 65.4% was mediated by solvent drag in the jejunum. Mannitol permeability was much more dependent on solvent drag in the colon (88.9%) than in the small intestine (65.4%). The net permeability rate of mannitol was similar in the jejunum and ileum but was much higher in the colon (P < 0.01). Addition of chenodeoxycholate (5 mM) to the perfusate resulted in a significant decrease in absorption of water (P < 0.01) with a corresponding decrease in mannitol permeability (P < 0.01). These studies indicate that mannitol permeability of the intestinal barrier is mediated by passive diffusion and solvent drag, with the latter accounting for a greater fraction of the total permeability.

摘要

甘露醇通常用作肠道通透性探针,但其穿透肠道屏障的机制尚不完全清楚。因此,我们研究了甘露醇在肠道不同节段的通透性,并在大鼠离体灌注肠段中研究了腔内因素对甘露醇体内通透性的动力学及影响。甘露醇的通透速率与其腔内浓度呈线性关系(y = 7.2x + 1.7;r = 0.98),表明被动扩散参与了甘露醇的通透过程。腔内液体渗透压从0.3 osmol/升增加到0.6 osmol/升,导致空肠和结肠的净水通量降低,同时甘露醇通透性相应降低(P < 0.01),表明溶剂拖曳对甘露醇净通透性有显著影响。在不同渗透压下,空肠和结肠中甘露醇通透性与水吸收之间的关系呈线性。在腔内渗透压为0.3 osmol/升时,空肠中34.6%的甘露醇通透由被动扩散介导,65.4%由溶剂拖曳介导。与小肠(65.4%)相比,结肠中甘露醇通透性对溶剂拖曳的依赖性更强(88.9%)。甘露醇的净通透速率在空肠和回肠中相似,但在结肠中要高得多(P < 0.01)。向灌注液中添加鹅去氧胆酸(5 mM)导致水吸收显著降低(P < 0.01),同时甘露醇通透性相应降低(P < 0.01)。这些研究表明,肠道屏障对甘露醇的通透性由被动扩散和溶剂拖曳介导,后者在总通透性中占更大比例。

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