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Functional roles and regulation of gastrointestinal transporter proteins in urea-nitrogen salvaging in ruminants

Functional roles and regulation of gastrointestinal transporter proteins in urea-nitrogen salvaging in ruminants
胃肠道转运蛋白在反刍动物尿素氮回收中的功能作用和调节
批准号:
RGPIN-2014-03766
负责人:
Mutsvangwa, Timothy
金额:
$1.89万
依托单位:
依托单位国家:
加拿大
项目类别:
Discovery Grants Program - Individual
财政年份:
2014
资助国家:
加拿大
项目状态:
已结题
起止时间:
2014-01-01 至 2015-12-31

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中文摘要
翻译
在驯养的反刍动物中,如牛肉和奶牛,饮食中提供的蛋白质含有生产肉和牛奶等可食用产品所需的氨基酸。然而,将膳食蛋白质转化为牛奶或肉类蛋白质的效率很差,仅为15 - 30%;换句话说,牛肉或奶牛摄入的大部分膳食蛋白质都以一种或另一种形式通过粪便排出体外。饲料中蛋白质在粪便中的过量排泄是不可取的,原因有很多,包括:1)蛋白质补充剂价格昂贵,因此从经济角度考虑,动物有效利用它们是很重要的;2)粪便中的蛋白质排泄对环境构成威胁。反刍动物的消化道与非反刍动物(如猪)的消化道不同,反刍动物的胃有四个隔室,前三个隔室分别是瘤胃、网状胃和瓣胃(统称为前胃)。在前胃中,有非常多样化的微生物群体发酵饲料。在某种程度上,饮食蛋白质利用效率低下是因为前胃中的微生物将大量饮食蛋白质发酵成氨,然后被吸收到血液中。氨对动物是有毒的,所以当血液从前胃流过肝脏时,基本上所有的氨都被肝脏排出。肝脏将氨转化为尿素,这是一种无毒的最终产物。在肝脏中产生的尿素被释放到血液中,其中大部分最终随尿液排出,因此代表了氮(最初包含在饮食蛋白质中)对动物的不可逆转的损失。然而,反刍动物已经进化出一种机制,允许血液中的尿素进入前胃,微生物可以利用它来促进自己的生长。这对动物是有益的,因为这些微生物最终会从前胃进入小肠,在那里它们被动物的酶消化,产生氨基酸,然后被吸收,用于生产牛奶和肉类。这个研究项目的主要目标是增强我们对尿素从血液进入前胃的控制机制的理解。目前我们所知道的是有两种蛋白质分子被称为尿素转运蛋白和水通道蛋白它们存在于前胃壁中似乎负责尿素从血液进入前胃;然而,我们不知道是什么控制着这些蛋白质分子的活性。在这个研究项目中,我将研究这些蛋白质分子的活性如何受到饲料组成、前胃发酵产物和激素的影响。如果我们能理解是什么营养或生理因素调节了这些蛋白质分子的活动,那么我们就能制定策略,增加尿素从血液进入前胃的通道。这将提高集约化反刍动物生产系统中饲粮蛋白质的利用率和环境管理。
英文摘要
In domesticated ruminants like beef and dairy cattle, the protein that is provided in the diet contains amino acids that are required for the production of edible products like meat and milk. However, the efficiency of converting dietary protein into milk or meat protein is poor at only 15 to 30%; in other words, most of the dietary protein that is consumed by beef or dairy cattle is excreted in the manure in one form or another. This excessive excretion of diet protein in the manure is undesirable for a number of reasons, including: 1) protein supplements are expensive, so it is important for economic reasons that animals use them efficiently; and 2) protein excretion in manure poses a threat to the environment. The ruminant digestive tract is different from that of non-ruminants (e.g., pigs) in that ruminants possess a four-compartment stomach, with the first three compartments being the rumen, reticulum, and omasum (collectively referred to as the fore-stomachs). In the fore-stomachs, there is a very diverse population of microorganisms that ferments the feed. In part, the inefficiency of dietary protein utilization arises because microorganisms in the fore-stomachs ferment a lot of the dietary protein to ammonia, which is then absorbed into the bloodstream. Ammonia is toxic to the animal, so essentially all of the ammonia is removed by the liver when blood from the fore-stomachs passes through the liver. The liver converts ammonia to urea, which is a non-toxic end-product. Urea that is produced in the liver is released into the bloodstream and most of it ends up being excreted in the urine, thus representing an irreversible loss of nitrogen (originally contained in dietary protein) to the animal. However, ruminants have evolved a mechanism that allows urea in the bloodstream to pass into the fore-stomachs where it can be used by the microorganisms for their own growth. This benefits the animal because these microorganisms eventually pass out of the fore-stomachs to the small intestine where they are digested by the animal’s enzymes to yield amino acids that are then absorbed and can be used for milk and meat production. This research program’s broad objective is to enhance our understanding of what controls the passage of urea from the bloodstream into the fore-stomachs. What we know at this time is that there are two types of protein molecules that are referred to as urea transporters and aquaporins that are found in the wall of the fore-stomachs and appear to be responsible for the passage of urea from the bloodstream into the fore-stomachs; however, we do not know what controls the activity of these protein molecules. In this research program, I will study how the activity of these protein molecules is affected by the composition of the diet, the products of fermentation in the fore-stomachs, and hormones. If we can understand what nutritional or physiological factors regulate the activity of these protein molecules, then we can develop strategies to increase the passage of urea from the bloodstream into the fore-stomachs. This would improve the utilization of diet protein and environmental stewardship in intensive ruminant production systems.
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The Molecular Regulation of Urea-Nitrogen Salvaging in Ruminants
  • 批准号:
    RGPIN-2019-04011
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $3.42万
  • 财政年份:
    2022
  • 负责人:
    Mutsvangwa, Timothy
  • 依托单位:
Evaluating whole flaxseed and flaxseed meals as energy and protein sources for high-producing dairy cows
  • 批准号:
    555747-2020
  • 项目类别:
    Alliance Grants
  • 资助金额:
    $3.42万
  • 财政年份:
    2021
  • 负责人:
    Mutsvangwa, Timothy
  • 依托单位:
The Molecular Regulation of Urea-Nitrogen Salvaging in Ruminants
  • 批准号:
    RGPIN-2019-04011
  • 项目类别:
    Discovery Grants Program - Individual
  • 资助金额:
    $3.42万
  • 财政年份:
    2021
  • 负责人:
    Mutsvangwa, Timothy
  • 依托单位:
Evaluating whole flaxseed and flaxseed meals as energy and protein sources for high-producing dairy cows
  • 批准号:
    555747-2020
  • 项目类别:
    Alliance Grants
  • 资助金额:
    $4.34万
  • 财政年份:
    2020
  • 负责人:
    Mutsvangwa, Timothy
  • 依托单位:
海外基金