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胃窦切除术或门腔分流术对大鼠胃泌酸黏膜中组胺储存内分泌样细胞的影响。荧光组织化学、电子显微镜及化学研究。

Effects of antrectomy or porta-caval shunting on the histamine-storing endocrine-like cells in oxyntic mucosa of rat stomach. A fluorescence histochemical, electron microscopic and chemical study.

作者信息

Häkanson R, Larsson L I, Liedberg G, Oscarson J, Sundler F, Vang J

出版信息

J Physiol. 1976 Aug;259(3):785-800. doi: 10.1113/jphysiol.1976.sp011495.

DOI:10.1113/jphysiol.1976.sp011495
PMID:957264
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1309064/
Abstract
  1. The argyrophil (enterochromaffin-like) cells in the oxyntic gland area of the rat stomach contain histamine, which can be demonstrated fluorescence microscopically after exposure to gaseous OPT. After administration of L-dopa (or L-5-hydroxytryptophan), these cells produce and temporarily store dopamine (or 5-hydroxytryptamine), demonstrable by its characteristic formaldehyde-induced fluorescence. Ultrastructurally, the enterochromaffin-like cells, which have the appearance of polypeptide hormone-secreting cells, comprise two main cell types, the most predominant one having vesicular type granules (EGL cells), the second most predominant one having smaller, uniformly electron dense granules (A-like cells). 2. Rats were subjected to the following surgical treatments: antrectomy; porta-caval shunting; antrectomy+porta-caval shunting; or sham-operation. Three to eight weeks after surgery the histamine-storing cells (enterochromaffin-like cells) of the oxyntic mucosa were analysed by fluorescence histochemistry, light and (quantitative) electron microscopy, and fluorometric determination of amines. 3. After antrectomy, fluorescence histochemistry and silver staining revealed a reduced number of enterochromaffin-like cells. The histamine content in the oxyntic mucosa was reduced by about 50%. As in unoperated injection of pentagastrin seemed to mobilize histamine. Feeding or injection of insulin failed to do so in antrectomized as opposed to control rats. Ultrastructurally, the cytoplasmic granules of both endocrine-like cell types were less numerous than in the unoperated rats. The reduction in cell number and granularity was particularly conspicuous with regard to the EGL cells. 4. After porta-caval shunting the number of enterochromaffin-like cells increased markedly. Chemical determination revealed a twofold increase in the histamine concentration of the oxyntic mucosa. Feeding or injection of insulin or pentagastrin lowered the histamine concentration. As judged by electron microscopy, the proliferation of endocrine-like cells induced by porta-caval shunting was restricted to the ECL cell type. Besides occurring in greater number, these cells were larger than those in unoperated controls, and their cytoplasm was densely packed with granules that were increased in size. 5. Following antrectomy of the porta-caval shunted rats the number of enterochromaffin-like cells and the oxyntic histamine concentration was reduced. 6. The results support the idea that gastrin exerts trophic as well as excitatory effects on oxyntic endocrine-like cells.
摘要
  1. 大鼠胃泌酸腺区的嗜银(肠嗜铬样)细胞含有组胺,暴露于气态OPT后可通过荧光显微镜显示。给予左旋多巴(或L - 5 - 羟色氨酸)后,这些细胞产生并暂时储存多巴胺(或5 - 羟色胺),可通过其特征性的甲醛诱导荧光显示。超微结构上,肠嗜铬样细胞具有分泌多肽激素细胞的外观,包括两种主要细胞类型,最主要的一种具有囊泡型颗粒(EGL细胞),第二主要的一种具有较小的、电子密度均匀的颗粒(A样细胞)。2. 对大鼠进行以下手术治疗:胃窦切除术;门腔分流术;胃窦切除术 + 门腔分流术;或假手术。术后3至8周,通过荧光组织化学、光镜和(定量)电镜以及胺的荧光测定法分析泌酸黏膜中储存组胺的细胞(肠嗜铬样细胞)。3. 胃窦切除术后,荧光组织化学和银染色显示肠嗜铬样细胞数量减少。泌酸黏膜中的组胺含量降低约50%。与未手术的大鼠一样,注射五肽胃泌素似乎能动员组胺。与对照大鼠相反,给胃窦切除的大鼠喂食或注射胰岛素未能做到这一点。超微结构上,两种内分泌样细胞类型的胞质颗粒均比未手术的大鼠少。细胞数量和颗粒度的减少在EGL细胞方面尤为明显。4. 门腔分流术后,肠嗜铬样细胞数量明显增加。化学测定显示泌酸黏膜中组胺浓度增加了两倍。给胰岛素或五肽胃泌素喂食或注射可降低组胺浓度。通过电镜判断,门腔分流诱导的内分泌样细胞增殖仅限于ECL细胞类型。除了数量更多外这些细胞比未手术对照中的细胞更大,其细胞质中密集充满了尺寸增大的颗粒。5. 对门腔分流的大鼠进行胃窦切除术后,肠嗜铬样细胞数量和泌酸组胺浓度降低。6. 结果支持胃泌素对泌酸内分泌样细胞具有营养和兴奋作用这一观点。
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7443/1309064/5083dad15838/jphysiol00843-0228-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7443/1309064/1af9bb930b88/jphysiol00843-0224-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7443/1309064/3086cbfbfcf1/jphysiol00843-0225-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7443/1309064/c9a9b1e19458/jphysiol00843-0226-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7443/1309064/81124a37f147/jphysiol00843-0227-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7443/1309064/5083dad15838/jphysiol00843-0228-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7443/1309064/1af9bb930b88/jphysiol00843-0224-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7443/1309064/3086cbfbfcf1/jphysiol00843-0225-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7443/1309064/c9a9b1e19458/jphysiol00843-0226-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7443/1309064/81124a37f147/jphysiol00843-0227-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7443/1309064/5083dad15838/jphysiol00843-0228-a.jpg

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