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大鼠下颌下腺紧密连接通透性的自主神经调节。

Autonomic regulation of tight junctional permeability in the rat submandibular gland.

作者信息

Kawabe H, Takai N

机构信息

Osaka Dental University.

出版信息

J Osaka Dent Univ. 1990 Oct;24(2):121-34.

PMID:2130159
Abstract

The permeability of tight junctions to tracers having different molecular weights was investigated in the submandibular gland of rats stimulated parasympathetically, sympathetically, or both. Lactoperoxidase (82,000 daltons), horseradish peroxidase (40,000 daltons), and microperoxidase (1,630 daltons) were used as the tracers. The tracers were administered by close arterial infusion via the glandular artery, and their secretion into the saliva was quantified biochemically, and their secretory routes within the gland were determined histochemically at the electron microscopic level. Microperoxidase and horseradish peroxidase passed into the saliva by electrical stimulation of either the chorda or superior cervical ganglion, and the combined stimulation of both caused a larger output of both tracers. No output of lactoperoxidase into the saliva occurred with any type of nerve stimulation. Electron microscopic histochemical observations showed that molecules of molecular weight equal to or lower than that of horseradish peroxidase entered the lumen through the tight junctions between adjacent acinar cells following combined stimulations of chorda and superior cervical ganglion. These findings indicate that electrical stimulation of parasympathetic and sympathetic nerves causes an increase in tight junctional permeability of acinar cells to microperoxidase and horseradish peroxidase. Although the combined stimulation of parasympathetic and sympathetic nerves resulted in increased junctional permeability to these tracers, the junctions remained impermeable to larger molecules, i.e., lactoperoxidase.

摘要

在对大鼠下颌下腺进行副交感神经、交感神经或两者联合刺激的情况下,研究了紧密连接对具有不同分子量示踪剂的通透性。使用了乳过氧化物酶(82,000道尔顿)、辣根过氧化物酶(40,000道尔顿)和微过氧化物酶(1,630道尔顿)作为示踪剂。通过经由腺动脉进行近距离动脉灌注给予示踪剂,对其分泌到唾液中的情况进行生化定量,并在电子显微镜水平通过组织化学方法确定其在腺体内的分泌途径。通过对鼓索或颈上神经节进行电刺激,微过氧化物酶和辣根过氧化物酶进入唾液,并且两者联合刺激导致两种示踪剂的分泌量更大。在任何类型的神经刺激下,乳过氧化物酶都不会分泌到唾液中。电子显微镜组织化学观察表明,在鼓索和颈上神经节联合刺激后,分子量等于或低于辣根过氧化物酶的分子通过相邻腺泡细胞之间的紧密连接进入管腔。这些发现表明,副交感神经和交感神经的电刺激会导致腺泡细胞紧密连接对微过氧化物酶和辣根过氧化物酶的通透性增加。尽管副交感神经和交感神经联合刺激导致对这些示踪剂的连接通透性增加,但紧密连接对更大的分子(即乳过氧化物酶)仍然是不可通透的。

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