Hirakawa H, Kobayashi H, O'Briain D S, Puri P
Children's Research Centre, Our Lady's Hospital for Sick Children, Crumlin, Dublin, Ireland.
J Pediatr Gastroenterol Nutr. 1995 Jan;20(1):54-8. doi: 10.1097/00005176-199501000-00010.
We studied the internal anal sphincter (IAS) muscle from 10 patients with achalasia and five normal controls using histochemical staining for NADPH-diaphorase and acetylcholinesterase (AChE). Normal control IAS muscle contained occasional AChE-positive nerve fibers, whereas IAS achalasia specimens demonstrated prominent AChE-positive nerve fibers in muscle layers. NADPH-diaphorase activity was strongly expressed in nerves in the normal IAS muscle but was absent or scanty in the muscle of patients with IAS achalasia. Our findings of increased AChE-positive nerves and the absence of NADPH-diaphorase activity taken in conjunction with reports of abnormal peptidergic innervation indicate that complex neural abnormalities occur in IAS achalasia. The primary event remains obscure, but it is possible that a single defect, such as nitrergic nerve depletion, may lead to compensatory changes in the other nerve fibers.
我们使用烟酰胺腺嘌呤二核苷酸磷酸黄递酶(NADPH-d)和乙酰胆碱酯酶(AChE)组织化学染色法,对10例贲门失弛缓症患者和5例正常对照者的肛门内括约肌(IAS)进行了研究。正常对照者的IAS肌肉中偶尔可见AChE阳性神经纤维,而贲门失弛缓症患者的IAS标本在肌层可见明显的AChE阳性神经纤维。NADPH-d活性在正常IAS肌肉的神经中强烈表达,但在贲门失弛缓症患者的肌肉中缺乏或稀少。我们发现AChE阳性神经增加且NADPH-d活性缺失,结合肽能神经支配异常的报道,表明贲门失弛缓症患者的IAS存在复杂的神经异常。主要病因仍不清楚,但有可能单一缺陷,如氮能神经耗竭,可能导致其他神经纤维的代偿性变化。