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反刍动物营养专题研讨会:发酵酸吸收在瘤胃 pH 调节中的作用。

Ruminant Nutrition Symposium: Role of fermentation acid absorption in the regulation of ruminal pH.

机构信息

Institute of Veterinary Physiology, Free University of Berlin, D-14163 Berlin, Germany.

出版信息

J Anim Sci. 2011 Apr;89(4):1092-107. doi: 10.2527/jas.2010-3301. Epub 2010 Oct 15.

Abstract

Highly fermentable diets are rapidly converted to organic acids [i.e., short-chain fatty acids (SCFA) and lactic acid] within the rumen. The resulting release of protons can constitute a challenge to the ruminal ecosystem and animal health. Health disturbances, resulting from acidogenic diets, are classified as subacute and acute acidosis based on the degree of ruminal pH depression. Although increased acid production is a nutritionally desired effect of increased concentrate feeding, the accumulation of protons in the rumen is not. Consequently, mechanisms of proton removal and their quantitative importance are of major interest. Saliva buffers (i.e., bicarbonate, phosphate) have long been identified as important mechanisms for ruminal proton removal. An even larger proportion of protons appears to be removed from the rumen by SCFA absorption across the ruminal epithelium, making efficiency of SCFA absorption a key determinant for the individual susceptibility to subacute ruminal acidosis. Proceeding initially from a model of exclusively diffusional absorption of fermentation acids, several protein-dependent mechanisms have been discovered over the last 2 decades. Although the molecular identity of these proteins is mostly uncertain, apical acetate absorption is mediated, to a major degree, via acetate-bicarbonate exchange in addition to another nitrate-sensitive, bicarbonate-independent transport mechanism and lipophilic diffusion. Propionate and butyrate also show partially bicarbonate-dependent transport modes. Basolateral efflux of SCFA and their metabolites has to be mediated primarily by proteins and probably involves the monocarboxylate transporter (MCT1) and anion channels. Although the ruminal epithelium removes a large fraction of protons from the rumen, it also recycles protons to the rumen via apical sodium-proton exchanger, NHE. The latter is stimulated by ruminal SCFA absorption and salivary Na(+) secretion and protects epithelial integrity. Finally, SCFA absorption also accelerates urea transport into the rumen, which via ammonium recycling, may remove protons from rumen to the blood. Ammonium absorption into the blood is also stimulated by luminal SCFA. It is suggested that the interacting transport processes for SCFA, urea, and ammonia represent evolutionary adaptations of ruminants to actively coordinate energy fermentation, protein assimilation, and pH regulation in the rumen.

摘要

高度可发酵的饮食在瘤胃中迅速转化为有机酸[即短链脂肪酸 (SCFA) 和乳酸]。质子的释放会对瘤胃生态系统和动物健康构成挑战。由产酸饮食引起的健康紊乱根据瘤胃 pH 值下降的程度分为亚急性和急性酸中毒。尽管增加浓缩饲料的酸产量是营养上所期望的效果,但瘤胃中质子的积累并非如此。因此,质子去除的机制及其定量重要性是主要关注点。唾液缓冲剂(即碳酸氢盐、磷酸盐)长期以来一直被认为是瘤胃质子去除的重要机制。更多的质子似乎通过 SCFA 穿过瘤胃上皮的吸收从瘤胃中去除,因此 SCFA 吸收的效率是个体对亚急性瘤胃酸中毒易感性的关键决定因素。从发酵酸的扩散吸收的模型开始,在过去的 20 年中发现了几种依赖于蛋白质的机制。尽管这些蛋白质的分子身份大多不确定,但顶侧乙酸吸收主要通过乙酸-碳酸氢盐交换介导,此外还有另一种对硝酸盐敏感、不依赖于碳酸氢盐的运输机制和亲脂扩散。丙酸和丁酸也显示出部分依赖于碳酸氢盐的运输模式。SCFA 和其代谢物的基底外侧外排主要由蛋白质介导,可能涉及单羧酸转运蛋白 (MCT1) 和阴离子通道。尽管瘤胃上皮从瘤胃中去除了大量的质子,但它也通过顶侧钠-质子交换器(NHE)将质子循环回瘤胃。后者受瘤胃 SCFA 吸收和唾液 Na+分泌的刺激,并保护上皮完整性。最后,SCFA 吸收也加速了尿素向瘤胃的转运,通过铵的再循环,可能会将质子从瘤胃中去除到血液中。血液中铵的吸收也受到腔侧 SCFA 的刺激。有人认为,SCFA、尿素和氨的相互作用的转运过程是反刍动物为了积极协调瘤胃中的能量发酵、蛋白质同化和 pH 调节而进化出的适应。

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