24-26 November 2021
Online
Australia/Sydney timezone

Hepatic lipid composition in dietary models of high iron NAFLD investigated with Synchrotron Infrared and X-Ray Fluorescence microscopy

24 Nov 2021, 11:35
15m
Online

Online

Oral Biomedicine, Life science & Food Science Biomedicine, Life science & Food Science

Speakers

Mr Clinton Kidman (Curtin University)Dr Cyril Mamotte (Curtin University)

Description

Hepatocytes are essential for maintaining homeostasis of mammalian iron and lipid metabolism. Serious health consequences have been linked to dysregulation of both areas. One such consequence is non-alcoholic fatty liver disease (NAFLD). Approximately 30% of individuals with NAFLD demonstrate a moderate increase in hepatic iron; however, the mechanism and metabolic consequences remain under-investigated. We assessed the metabolic consequences using mice fed either a control or high fat (HF) diet, with or without high iron. Attenuated Total Reflection Infrared Microscopy (Macro-ATR) at the Australian Synchrotron was used to investigate lipid composition and distribution, and X-Ray Fluorescence Microscopy (XRF) at the Diamond Light Source (UK) was used to determine subcellular iron concentration and distribution. Peri-portal hepatocytes of HF fed animals exhibited elevated lipid parameters, including ester and free fatty acid concentrations ~7x that of controls (P<0.005). The increase was seen within lipid droplets, which were primarily composed of cholesteryl esters and triglycerides. When HF livers were iron loaded, reductions in all lipid parameters were observed, with ~2.6x lower relative ester concentration (P<0.05) compared to HF only. Iron loaded HF peri-portal hepatocytes exhibited shorter chain lengths (P<0.005) and a shift in the olefinic peak (3011 cm-1) compared to HF (3007 cm-1) (P<0.05), suggesting the shorter chains were more polyunsaturated. Iron accumulated within mitochondria of peri-portal hepatocytes of animals fed high iron diets. Poly-unsaturated lipids are strong activators of hepatic lipid breakdown and this study suggests a role for iron in reducing the lipid burden by remodelling hepatic lipids in NAFLD.

Presenter Gender Man
Students Only - Are you interested in AINSE student funding Yes
Do you wish to take part in the Student Poster Slam Yes
Level of Expertise Student
Which facility did you use for your research Australian Synchrotron
Pronouns He/Him
Condition of submission Yes

Primary author

Mr Clinton Kidman (Curtin University)

Co-authors

Dr Cyril Mamotte (Curtin University) Mr James Chasland (Curtin University) Keea Inder-Smith (Curtin University) Annaleise Klein (ANSTO) Jitraporn (Pimm) Vongsvivut (Australian Synchrotron) Martin de Jonge (ANSTO) Dr Mark Tobin (ANSTO) Mark John Hackett (Curtin University) Dr Ross Graham (Curtin University)

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