可乐水/乙醇豆荚提取物对脂多糖性腹泻炎症及肠道分泌的影响

Henri Wambe, P. A. Noubissi, Elvine Pami, Sorelle Mbankou Ngassam, J. M. Pouadjeu, Ariane Falone Goumtsa, Cédric Wamba Koho, Roger Hermann Sadie Foguieng, R. Kamgang, T. B. Nguelefack
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摘要

腹泻是低收入和中低收入国家儿童死亡的主要原因之一,在这些地区,对这种疾病的管理仍然是一个问题。可乐豆角(KEO)的水/乙醇提取物已被证明对福氏志贺氏菌引起的腹泻具有抗菌和止泻作用,但KEO是否对这种腹泻的毒性部分有活性尚不清楚。本研究旨在探讨KEO对腹腔注射脂多糖(LPS)引起的肠道分泌和炎症的影响。经水/乙醇(1:1)浸泡得到的KEO分别以25、50和100 mg/kg体重口服,用于lps诱导的小鼠腹泻。测定大鼠粪便质量、肠道一氧化氮(NO)、前列腺素(PGE2)含量及骨髓过氧化物酶(MPO)活性。KEO还对lps诱导的大鼠肠池化进行了实验。本试验测定大鼠小肠匀浆中肠液及其电解质(Na+、K+、Cl-)含量以及NO、PGE2、TNF-α、IL-1β水平。以吲哚美辛(5 mg/kg)为对照药。KEO显著(p < 0.001)降低了lps诱导腹泻的粪便排泄量、NO含量和肠道MPO活性,但不影响PGE2。在肠池模型中,KEO对大鼠肠液和电解质排泄及PGE2、TNF-α和IL-1β含量无显著影响,但显著(p < 0.05)降低了no的产生。本研究提示KEO不具有抗分泌作用,但具有抗炎活性。由此可见,在感染性腹泻中,KEO的抗毒作用对其止泻作用的贡献较小。
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Effects of Cola anomala (K. Schum.) water/ethanol pods extract on the inflammation and intestinal secretion in lipopolysaccharide-induced diarrhea
Diarrhea is one of the leading causes of death among children in low and low-middle income countries and the management of this pathology is still a problem in these regions. The water/ethanol extract of the pods of Cola anomala (KEO) has been shown to possess antimicrobial and antidiarrheal effects in Shigella flexneri-induced diarrhea, but whether KEO is active on the toxemic part of this diarrhea is unknown. This study was undertaken to evaluate the effects of KEO on the intestinal secretion and inflammation induced by intraperitoneal administration of lipopolysaccharide (LPS). KEO obtained by maceration in water/ethanol (1:1) was administered orally (25, 50 and 100 mg/kg of body weight) against LPS-induced diarrhea in mice. The mass of feces, the intestinal nitric oxide (NO) and prostaglandin (PGE2) contents as well as myeloperoxidase (MPO) activity were assessed. KEO was also tested on LPS-induced enteropooling in rats. In this experiment, the intestinal fluid and its electrolytes (Na+, K+ and Cl-) contents were determined as well as NO, PGE2, TNF-α and IL-1β levels in the small intestine homogenate. Indomethacin (5 mg/kg) was used as reference drug. KEO significantly (p < 0.001) reduced stools excretion, NO content and MPO activity in intestine but did not affect PGE2 in LPS-induced diarrhea. On the enteropooling model, KEO showed no effect on the intestinal fluid and electrolyte excretion, PGE2, TNF-α and IL-1β contents, but significantly (p < 0.05) reduced the NO production. This study suggests that KEO does not have antisecretory effect, but has anti inflammatory activities. It can be concluded that the anti-toxemic effect of KEO contributes less to its antidiarrheal activity in infectious diarrhea.
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