Young A, Levin R J
Department of Biology, Pharmaceutical Division, Reckitt & Colman, Kingston-upon-Hull.
Gut. 1990 Feb;31(2):162-9. doi: 10.1136/gut.31.2.162.
The effects of progressive starvation for up to three days on the basal and secretagogue stimulated secretory functions of the rat ileum were investigated in vitro and in vivo. The secretagogues used included agents acting via cyclic AMP (dibutyryl cyclic AMP, theophylline, forskolin, and PGE2) and those acting via Ca++ (acetylcholine, bethanecol, carbachol, 5-hydroxytryptamine, and A23187). Starving rats for 24 h (day 1) had no effect on the basal electrogenic secretion (measured as the short circuit current, Isc muamps/cm2) or on the stimulated maximum electrogenic secretion (measured as the delta Isc where delta Isc = maxIsc-basal Isc). By day 2 of starvation, however, both the basal Isc and the delta Isc induced by all the secretagogues were significantly greater than in the fed and increased even more on day 3. Replacement of all the chloride ions and inhibition by furosemide indicated that the enhanced secretion was due mainly to chloride ions. Cholinergic stimulation was blocked by atropine, indicating the stimulation was via muscarinic receptors while cholinergic dose - delta Isc response curves for fed and starved ilea showed significantly increased maximum electrogenic secretory response in the latter but no evidence of any change in the affinity (ED50) of the receptors mediating the response. The basal secretion and the secretory response to acetylcholine in both fed and starved ilea was unaffected by tetrodotoxin, revealing that the enhanced secretory response could be expressed via the muscarinic receptors on the enterocytes without the enteric neural network. Measurement of ileal fluid movement in vivo showed that in fed and day 1 starved rats the basal, unstimulated 'tone' of the ileum was absorptive. On day 2, however, the basal 'tone' had reversed to one of secretion which increased further on day 3. Stimulation of fluid secretion in vivo by bethanecol, carbachol, or PGE2 induced larger increases in the starved ilea by day 2 which increased even further on day 3. Lumenal chloride and bicarbonate concentrations were greater in the starved ileal fluid than in the fed. The studies in rat ileum confirm and extend those on rat jejunum and indicate that starvation creates a hypersensitive small bowel that responds to secretagogues and cholinergic neurotransmitters with a greatly enhanced secretory response.
研究了长达三天的渐进性饥饿对大鼠回肠基础分泌功能以及促分泌剂刺激的分泌功能的体内和体外影响。所用的促分泌剂包括通过环磷酸腺苷(二丁酰环磷酸腺苷、茶碱、福斯可林和前列腺素E2)起作用的药物,以及通过钙离子(乙酰胆碱、氨甲酰甲胆碱、卡巴胆碱、5-羟色胺和A23187)起作用的药物。饥饿24小时(第1天)的大鼠,其基础电分泌(以短路电流Isc微安/平方厘米衡量)或刺激后的最大电分泌(以ΔIsc衡量,其中ΔIsc = 最大Isc - 基础Isc)均未受影响。然而,到饥饿第2天时,所有促分泌剂诱导的基础Isc和ΔIsc均显著高于喂食组,且在第3天进一步增加。用所有氯离子替代物以及呋塞米抑制表明,增强的分泌主要归因于氯离子。胆碱能刺激被阿托品阻断,表明刺激是通过毒蕈碱受体介导的,而喂食和饥饿回肠的胆碱能剂量 - ΔIsc反应曲线显示,后者的最大电分泌反应显著增加,但介导反应的受体亲和力(半数有效剂量)没有任何变化的迹象。喂食和饥饿回肠的基础分泌以及对乙酰胆碱的分泌反应均不受河豚毒素影响,这表明增强的分泌反应可通过肠上皮细胞上的毒蕈碱受体表达,而无需肠神经网络。体内回肠液体运动测量显示,在喂食和饥饿第1天的大鼠中,回肠的基础、未受刺激的“张力”是吸收性的。然而,在第2天,基础“张力”转变为分泌性,且在第3天进一步增加。氨甲酰甲胆碱、卡巴胆碱或前列腺素E2在体内刺激液体分泌,到第2天时,饥饿回肠的增加幅度更大,且在第3天进一步增加。饥饿回肠液中的管腔氯离子和碳酸氢盐浓度高于喂食组。对大鼠回肠的研究证实并扩展了对大鼠空肠的研究,表明饥饿会导致小肠超敏,使其对促分泌剂和胆碱能神经递质产生大大增强的分泌反应。