Peter Zahradka

Has grant

professor

University of Manitoba
Country flagCanada

Research Interests

Explore related searches

Contact this professor

Get a free first email built on one of their papers, ready for you to edit and send yourself.

About

Peter Zahradka is a professor at the University of Manitoba in Canada. His research primarily focuses on the effects of dietary components on vascular health, obesity, and metabolic processes, as exemplified by his recent studies on the impacts of wheat and black bean consumption, zinc deficiency, and omega-3 fatty acids. His work contributes to the understanding of nutritional interventions in the management of chronic health conditions.

Recent Grants

Grant: Close

Hormonal mechanisms of gene regulation

Open Date: 2014-04-01

Close Date: 2015-03-31

Grant: Close

Effect of c9,t11-conjugated linoleic acid (CLA) on insulin sensitivity of skeletal muscle

Open Date: 2011-04-01

Close Date: 2012-03-31

Grant: Close

Multicisciplianaire training program in health-food industry and technology (FAST)

Open Date: 2010-04-01

Close Date: 2015-03-31

Grant: Close

Isolation and characterization of a pulse crop-derived bioactive that improves arterial stiffness

Open Date: 2010-04-01

Close Date: 2013-03-31

Grant: Close

Hormonal mechanisms of gene regulation

Open Date: 2009-04-01

Close Date: 2014-03-31

Articles (12)

Year:

2025

Polyunsaturated fatty acids (PUFAs) can alter adipose tissue function; however, the relative effects of plant and marine n3-PUFAs are less clear. Our objective was to directly compare the n3-PUFAs, plant-based α-linolenic acid (ALA) in flaxseed oil, and marine-based eicosapentaenoic acid (EPA) or docosahexaenoic acid (DHA) in high-purity oils versus n6-PUFA containing linoleic acid (LA) for their effects on the adipose tissue and oral glucose tolerance of obese rats. Male fa/fa Zucker rats were assigned to faALA, faEPA, faDHA, and faLA groups and compared to baseline fa/fa rats (faBASE) and lean Zucker rats (lnLA). After 8 weeks, faEPA and faDHA had 11–14% lower body weight than faLA. The oral glucose tolerance and total body fat were unchanged, but faEPA had less mesenteric fat. faEPA and faDHA had fewer large adipocytes compared to faLA and faALA. EPA reduced macrophages in the adipose tissue of fa/fa rats compared to ALA and DHA, while faLA had the greatest macrophage infiltration. DHA decreased (~10-fold) T-cell infiltration compared to faBASE and faEPA, whereas faALA and faLA had an ~40% increase. The n3-PUFA diets attenuated tumour necrosis factor-α in adipose tissue compared to faBASE, while it was increased by LA in both genotypes. In conclusion, EPA and DHA target different aspects of inflammation in adipose tissue.

Year:

2024

Year:

2024

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Year:

2021

Year:

2021

Year:

2021

Year:

2020

Year:

2020

Collaborators (3)

Carla G. Taylor

University of Manitoba

CANADA
View details

Samantha Pauls

Assistant Professor

University of Manitoba

CANADA
View details

Sheila West

Professor

Pennsylvania State University

UNITED STATES
View details
ApplyKite TwinLearns as you apply

Make your next move.

Prepare your application

Review drafts before you send them.