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Aging Cell. 2016 Aug;15(4):706-15. doi: 10.1111/acel.12481. Epub 2016 Apr 20.

Ultrastructure of the liver microcirculation influences hepatic and systemic insulin activity and provides a mechanism for age-related insulin resistance.

Author information

1
Ageing and Alzheimers Institute, Centre for Education and Research on Ageing, University of Sydney and Concord Hospital, Sydney, NSW, Australia.
2
ANZAC Research Institute, University of Sydney and Concord Hospital, Sydney, NSW, Australia.
3
Faculty of Pharmacy, Universiti Teknologi MARA, Selangor, Malaysia.
4
Translational Gerontology Branch, National Institute on Aging, National Institutes of Health, Baltimore, MD, USA.
5
Laboratory for Ageing Research, School of Medical Sciences, University of New South Wales, Sydney, NSW, Australia.
6
Charles Perkins Centre, University of Sydney, Sydney, NSW, Australia.
7
Kolling Institute of Medical Research, Royal North Shore Hospital and University of Sydney, Sydney, NSW, Australia.
8
Department of Pathology, University of Otago, Christchurch, New Zealand.
9
Department of Genetics, Harvard Medical School, Boston, MA, USA.

Abstract

While age-related insulin resistance and hyperinsulinemia are usually considered to be secondary to changes in muscle, the liver also plays a key role in whole-body insulin handling and its role in age-related changes in insulin homeostasis is largely unknown. Here, we show that patent pores called 'fenestrations' are essential for insulin transfer across the liver sinusoidal endothelium and that age-related loss of fenestrations causes an impaired insulin clearance and hyperinsulinemia, induces hepatic insulin resistance, impairs hepatic insulin signaling, and deranges glucose homeostasis. To further define the role of fenestrations in hepatic insulin signaling without any of the long-term adaptive responses that occur with aging, we induced acute defenestration using poloxamer 407 (P407), and this replicated many of the age-related changes in hepatic glucose and insulin handling. Loss of fenestrations in the liver sinusoidal endothelium is a hallmark of aging that has previously been shown to cause deficits in hepatic drug and lipoprotein metabolism and now insulin. Liver defenestration thus provides a new mechanism that potentially contributes to age-related insulin resistance.

KEYWORDS:

ageing; aging; endothelium; fenestrae; fenestrations; hyperinsulinemia

PMID:
27095270
PMCID:
PMC4933657
DOI:
10.1111/acel.12481
[Indexed for MEDLINE]
Free PMC Article

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