Physiological relevance of enterocytic lipid trafficking pathways on dietary lipid absorption and whole body lipid homeostasis
肠细胞脂质运输途径对膳食脂质吸收和全身脂质稳态的生理相关性
基本信息
- 批准号:RGPIN-2015-03971
- 负责人:
- 金额:$ 3.57万
- 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:2016
- 资助国家:加拿大
- 起止时间:2016-01-01 至 2017-12-31
- 项目状态:已结题
- 来源:
- 关键词:
项目摘要
PROGRAM SCOPE
The gastrointestinal tract is the 'first-pass' organ for the metabolism of dietary fats and has an important role in regulation of lipids and cholesterol throughout the whole body. Over the past 10 years of NSERC funding, my group has contributed to new insights into the regulation of intestinal absorption and secretion by dietary lipids. By combining a unique series of technical (absorption/transport) and (production/secretory) methods, we have made landmark discoveries that have wide-ranging impact in the community; including engaging Health Canada on food policies, having leadership roles with provincial, national and international Livestock/Dairy sector, underpinning business plan of the pharmaceutical industry and contributed to emerging molecular pathways for new drug targets via the intestine. The contributions of my NSERC program have trained a significant number of graduate and undergraduate students from all over the world, who have gone on to take positions in other University's, industry and government.
SIGNIFICANCE AND NOVELTY
The gastrointestinal tract includes a unique series of conduit vessels (called the lymphatics) that not only facilitate the inflammatory cell network but are also critical to transport dietary fats into the blood stream. The ability to carefully cannulate the primary lymphatic duct (in rodents and recently in swine) enables the study of the lymphatic system and its role in nutrition. We have exciting new data that shows two lipid fractions found in the lymphatics (large lipid molecules called chylomicrons and smaller 'good cholesterol' HDL particles) can be altered during fed state, and contain a high abundance of novel genetic material called microRNAs. The significance of lymphatic-associated microRNA’s is that it provides new evidence of how the intestine may regulate lipids in the body.
OBJECTIVES OF NSERC PROGRAM
The focus of the renewal to my NSERC program is to propose that the lymphatic system plays a critical role in two major pathways that control lipid metabolism in the body; (1) It can regulate good forms of cholesterol (HDL) in the removal of 'bad' forms of cholesterol from the body via the ‘reverse-cholesterol transport’ [RCT] pathway and (2) via a new pathway called trans-intestinal cholesterol efflux [TICE]. TICE is an emerging concept suggesting that the intestine effluxes blood-derived cholesterol into the lumen for excretion out of the body. New data suggests that the TICE pathway contributes significantly to cholesterol metabolism in the body and can be modulated by nutrients. Recently, it has also been discovered that disruption to the lymphatic system leads to an impairment of RCT and possibly TICE. Through this NSERC program we will discover how the lymphatic system links these pathways, how miRNAs, nutrients or compounds may modulate these pathways during normal lipid homeostasis.
项目范围
项目成果
期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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Proctor, Spencer其他文献
Pioglitazone inhibits HIF-1α-dependent angiogenesis in rats by paracrine and direct effects on endothelial cells.
- DOI:
10.1007/s00109-013-1115-0 - 发表时间:
2014-05 - 期刊:
- 影响因子:4.7
- 作者:
Dromparis, Peter;Sutendra, Gopinath;Paulin, Roxane;Proctor, Spencer;Michelakis, Evangelos D.;McMurtry, M. Sean - 通讯作者:
McMurtry, M. Sean
Proctor, Spencer的其他文献
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{{ truncateString('Proctor, Spencer', 18)}}的其他基金
Novel roles of the intestine to regulate whole body lipid homeostasis using pathways of nutritional physiology and molecular regulation.
肠道利用营养生理学和分子调节途径调节全身脂质稳态的新作用。
- 批准号:
RGPIN-2021-03871 - 财政年份:2022
- 资助金额:
$ 3.57万 - 项目类别:
Discovery Grants Program - Individual
Novel roles of the intestine to regulate whole body lipid homeostasis using pathways of nutritional physiology and molecular regulation.
肠道利用营养生理学和分子调节途径调节全身脂质稳态的新作用。
- 批准号:
RGPIN-2021-03871 - 财政年份:2021
- 资助金额:
$ 3.57万 - 项目类别:
Discovery Grants Program - Individual
Physiological relevance of enterocytic lipid trafficking pathways on dietary lipid absorption and whole body lipid homeostasis
肠细胞脂质运输途径对膳食脂质吸收和全身脂质稳态的生理相关性
- 批准号:
RGPIN-2015-03971 - 财政年份:2019
- 资助金额:
$ 3.57万 - 项目类别:
Discovery Grants Program - Individual
Physiological relevance of enterocytic lipid trafficking pathways on dietary lipid absorption and whole body lipid homeostasis
肠细胞脂质运输途径对膳食脂质吸收和全身脂质稳态的生理相关性
- 批准号:
RGPIN-2015-03971 - 财政年份:2018
- 资助金额:
$ 3.57万 - 项目类别:
Discovery Grants Program - Individual
Physiological relevance of enterocytic lipid trafficking pathways on dietary lipid absorption and whole body lipid homeostasis
肠细胞脂质运输途径对膳食脂质吸收和全身脂质稳态的生理相关性
- 批准号:
RGPIN-2015-03971 - 财政年份:2017
- 资助金额:
$ 3.57万 - 项目类别:
Discovery Grants Program - Individual
Physiological relevance of enterocytic lipid trafficking pathways on dietary lipid absorption and whole body lipid homeostasis
肠细胞脂质运输途径对膳食脂质吸收和全身脂质稳态的生理相关性
- 批准号:
RGPIN-2015-03971 - 财政年份:2015
- 资助金额:
$ 3.57万 - 项目类别:
Discovery Grants Program - Individual
Enterocyte lipid trafficking pathways that regulate intestinal absorption and efflux of dietary lipids
调节肠道吸收和膳食脂质流出的肠细胞脂质运输途径
- 批准号:
312056-2010 - 财政年份:2014
- 资助金额:
$ 3.57万 - 项目类别:
Discovery Grants Program - Individual
Enterocyte lipid trafficking pathways that regulate intestinal absorption and efflux of dietary lipids
调节肠道吸收和膳食脂质流出的肠细胞脂质运输途径
- 批准号:
312056-2010 - 财政年份:2013
- 资助金额:
$ 3.57万 - 项目类别:
Discovery Grants Program - Individual
Enterocyte lipid trafficking pathways that regulate intestinal absorption and efflux of dietary lipids
调节肠道吸收和膳食脂质流出的肠细胞脂质运输途径
- 批准号:
312056-2010 - 财政年份:2012
- 资助金额:
$ 3.57万 - 项目类别:
Discovery Grants Program - Individual
Enterocyte lipid trafficking pathways that regulate intestinal absorption and efflux of dietary lipids
调节肠道吸收和膳食脂质流出的肠细胞脂质运输途径
- 批准号:
312056-2010 - 财政年份:2011
- 资助金额:
$ 3.57万 - 项目类别:
Discovery Grants Program - Individual
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