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利多卡因对犬十二指肠中对腔内化学刺激产生反应的CCK-PZ和分泌素分泌旁神经元的影响(作者译)

[Effects of lidocaine upon CCK-PZ and secretin producing paraneurons in the canine duodenum responding to luminal chemical stimuli (author's transl)].

作者信息

Sato K, Muraki S, Fujita T, Noguchi R, Shimoji K

出版信息

No To Shinkei. 1982 Apr;34(4):375-81.

PMID:7093074
Abstract

Amino acid solution (50 mM tryptophan and 50 mM phenylalanine in saline) introduced into the canine duodenal loop causes an increased enzyme output from the pancreas, whereas administration of 0.1 N HCl into the duodenal loop causes an increased juice flow from the organ. Local anesthetic, lidocaine, introduced into the duodenal lumen suppressed the pancreatic enzyme releasing response to the intraluminal amino acid without affecting the juice flow response to the hydrochloric stimulus. Intravenously administered lidocaine did not block the pancreatic response to the intraluminal amino acid stimulus, suggesting that lidocaine affects the chemoreceptive, apical part of the endocrine cell or paraneuron which releases cholecystokinin-pancreozymin (CCK-PZ). Neither was the pancreas responding to an intravenous injection of CCK-PZ (5 Ivy Dog Units) suppressed by intravenously administered lidocaine even when its arterial concentration exceeded the convulsion level. This indicates that lidocaine affects the duodenal paraneurons recognizing the luminal stimuli but not the pancreatic cells responding to the hormones released by them. The results further suggest that in paraneurons as well as in neurons there seems to be a spectrum with regard to the susceptibility to anesthetics; thus the secretin releasing paraneuron is much more resistant to lidocaine than the CCK-PZ producing one.

摘要

将氨基酸溶液(盐水中含50 mM色氨酸和50 mM苯丙氨酸)注入犬十二指肠肠袢会导致胰腺的酶分泌增加,而向十二指肠肠袢注入0.1 N盐酸会使该器官的胰液分泌增加。将局部麻醉药利多卡因注入十二指肠腔可抑制胰腺对腔内氨基酸的酶释放反应,而不影响对盐酸刺激的胰液分泌反应。静脉注射利多卡因不会阻断胰腺对腔内氨基酸刺激的反应,这表明利多卡因影响释放胆囊收缩素-促胰酶素(CCK-PZ)的内分泌细胞或副神经元的化学感受性顶端部分。即使静脉注射利多卡因后其动脉血浓度超过惊厥水平,静脉注射CCK-PZ(5个艾维犬单位)时胰腺的反应也不会受到抑制。这表明利多卡因影响识别腔内刺激的十二指肠副神经元,但不影响对它们释放的激素作出反应的胰腺细胞。结果还进一步表明,副神经元和神经元一样,对麻醉药的敏感性似乎存在一个范围;因此,释放促胰液素的副神经元比产生CCK-PZ的副神经元对利多卡因的耐受性要强得多。

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