Department of Physiology, Institute of Medical Sciences, Banaras Hindu University, Varanasi 221005, UP, India.
J Pediatr Surg. 2009 Nov;44(11):2156-62. doi: 10.1016/j.jpedsurg.2009.04.032.
Congenital pouch colon (CPC) associated with anorectal malformation (ARM) is most commonly reported from Northern India. So far, no physiologic study comparing the detailed contractile status of CPC with non-CPC conditions are available. The present article deals with the contractile study and histopathologic observations in CPC, which may be useful for better surgical management.
Freshly excised 12 neonatal CPC and similar number of non-CPC (control) specimens were transferred to ice-cold (4 degrees C-6 degrees C) Krebs-Ringer solution bubbled with 100% oxygen. Longitudinally prepared 2 to 4 colonic strips were obtained from central part of each specimen and subjected to the contraction recording after exposure to cumulative concentrations of acetylcholine (ACh) and histamine. Acetylcholine-induced contractions were evaluated after application of atropine (muscarinic blocker), and histaminergic contractions were recorded after pheniramine (H(1) blocker), lignocaine (neuronal blocker), and atropine. Histopathologic observations were made by using H&E and Masson trichrome stains.
Control specimens showed spontaneous contractions, but CPC strips did not. Both control and CPC responded to ACh and histamine. The response to histamine was greater (P < .05) in CPC as compared to control, whereas the response to ACh was more (P < .05) in control. In CPC, response of histamine (100 micromol/L) was blocked by pheniramine (0.32 mmol/L) and lignocaine (4 mmol/L) by 97% and 80%, respectively, and enhanced by 57% after preapplication of atropine (10 micromol/L). Acetylcholine (100 micromol/L)-induced contractions were attenuated (86%) in presence of atropine. Histopathologic examination showed fewer mature ganglion cells with various changes in muscle layers including fibrosis, disruption, hypertrophy, atrophy, and constriction bands.
Congenital pouch colon associated with ARM lacks normal spontaneous contractions but retains ACh and histamine-induced contractility. In view of the functional and histologic abnormalities, we propose that CPC associated with ARM is an abnormally functional and developed tissue. Therefore, resection of the pouch should be considered for better functional outcome of the remaining bowel.
先天性囊状结肠(CPC)与肛门直肠畸形(ARM)相关,在印度北部最为常见。到目前为止,尚无比较 CPC 与非 CPC 条件下详细收缩状态的生理学研究。本文涉及 CPC 的收缩研究和组织病理学观察,这可能有助于更好的手术治疗。
将 12 个新鲜切除的新生儿 CPC 和数量相同的非 CPC(对照)标本转移到冰冷(4 摄氏度至 6 摄氏度)的 Krebs-Ringer 溶液中,溶液用 100%氧气充气。从每个标本的中央部分获得 2 到 4 个结肠条,并在暴露于累积浓度的乙酰胆碱(ACh)和组氨酸后进行收缩记录。在应用阿托品(毒蕈碱阻滞剂)后评估乙酰胆碱诱导的收缩,并且在应用苯海拉明(H1 阻滞剂)、利多卡因(神经元阻滞剂)和阿托品后记录组氨酸能收缩。使用 H&E 和 Masson 三色染色进行组织病理学观察。
对照标本显示自发性收缩,但 CPC 条带没有。对照和 CPC 均对 ACh 和组氨酸有反应。与对照相比,CPC 对组氨酸的反应更大(P<0.05),而对照中对 ACh 的反应更大(P<0.05)。在 CPC 中,组胺(100μmol/L)的反应被苯海拉明(0.32mmol/L)和利多卡因(4mmol/L)分别阻断 97%和 80%,并且在用 10μmol/L 的阿托品预处理后增强 57%。在存在阿托品的情况下,乙酰胆碱(100μmol/L)诱导的收缩被减弱(86%)。组织病理学检查显示成熟神经节细胞较少,肌肉层有各种变化,包括纤维化、破坏、肥大、萎缩和收缩带。
与 ARM 相关的先天性囊状结肠缺乏正常的自发性收缩,但保留 ACh 和组氨酸诱导的收缩性。鉴于功能和组织学异常,我们提出与 ARM 相关的 CPC 是一种异常功能和发育的组织。因此,应考虑切除袋状结构以获得更好的剩余肠道功能。