本构性基础和受刺激的人小肠收缩力在肥胖中增强。

Tom K Gallagher, Alan W Baird, Desmond C Winter
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引用次数: 16

摘要

肥胖受试者的小肠收缩可能更为突出,从而增强营养吸收和饥饿感刺激。然而,几乎没有证据支持这一观点。这项研究检查了肥胖患者与非肥胖患者的体外小肠收缩性。在腹腔镜Roux-en-Y胃旁路术中从肥胖患者获得组织学正常的小肠样本。对照标本取自因良性疾病或形成回肠袋-肛门吻合术而行小肠切除术的非肥胖患者。样品在预充氧的克雷布斯溶液中运输。将微解剖的圆形平滑肌条在1 g张力下悬浮于含有95% O2/5% CO2的克雷布斯溶液的器官液中,温度为37℃。在基线时使用等长传感器记录收缩活性,并在模糊和非肾上腺素能、非胆碱能条件下(胍乙啶和阿托品)使用前列腺素F2a、一氧化氮供体和P物质响应受体介导的收缩活性。平衡后,肥胖组(n = 63)对胆碱能激动剂carbachol (0.1 mmol/L)的初始反应显著高于瘦组(n = 61),平均最大反应:体重比为4.58 +/- 0.89 vs 3.53 +/- 0.74;(p = 0.032)。在洗脱和重新校准后,P物质和前列腺素F2a的累积应用产生了人小肠平滑肌条的浓度依赖性收缩。与非肥胖小肠相比,肥胖小肠在模棱两可条件下的收缩反应显著增加(所有激动剂均p < 0.05)。然而,当实验在NANC条件下进行时,各组之间没有显着差异。在模棱两可或NANC条件下,两组之间在一氧化氮刺激下没有发现显著差异。肥胖患者受刺激的小肠收缩力增加,提示肠道排空更快,肠道运输更快。这可能会导致食欲增强和饱腹感降低。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Constitutive basal and stimulated human small bowel contractility is enhanced in obesity.

Constitutive basal and stimulated human small bowel contractility is enhanced in obesity.

Constitutive basal and stimulated human small bowel contractility is enhanced in obesity.

Constitutive basal and stimulated human small bowel contractility is enhanced in obesity.

Small bowel contractility may be more prominent in obese subjects, such that there is enhanced nutrient absorption and hunger stimulation. However, there is little evidence to support this. This study examined in vitro small bowel contractility in obese patients versus non-obese patients. Samples of histologically normal small bowel were obtained at laparoscopic Roux-en-Y gastric bypass from obese patients. Control specimens were taken from non-obese patients undergoing small bowel resection for benign disease or formation of an ileal pouch-anal anastomosis. Samples were transported in a pre-oxygenated Krebs solution. Microdissected circular smooth muscle strips were suspended under 1 g of tension in organ baths containing Krebs solution oxygenated with 95% O2/5% CO2 at 37 degrees C. Contractile activity was recorded using isometric transducers at baseline and in response to receptor-mediated contractility using prostaglandin F2a, a nitric oxide donor and substance P under both equivocal and non-adrenergic, non-cholinergic conditions (guanethidine and atropine). Following equilibration, the initial response to the cholinergic agonist carbachol (0.1 mmol/L) was significantly increased in the obese group (n = 63) versus the lean group (n = 61) with a mean maximum response: weight ratio of 4.58 +/- 0.89 vs 3.53 +/- 0.74; (p = 0.032). Following washout and re-calibration, cumulative application of substance P and prostaglandin F2a produced concentration-dependent contractions of human small bowel smooth muscle strips. Contractile responses of obese small bowel under equivocal conditions were significantly increased compared with non-obese small bowel (p < 0.05 for all agonists). However, no significant differences were shown between the groups when the experiments were performed under NANC conditions. There were no significant differences found between the groups when challenged with nitric oxide, under either equivocal or NANC conditions. Stimulated human small bowel contractility is increased in obese patients suggesting faster enteric emptying and more rapid intestinal transit. This may translate into enhanced appetite and reduced satiety.

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