Literature DB >> 17144886

Vascular function in the metabolic syndrome and the effects on skeletal muscle perfusion: lessons from the obese Zucker rat.

Jefferson C Frisbee1, Michael D Delp.   

Abstract

The increased prevalence of obesity in Western society has been well established for many years, and with this trend, the prevalence of other associated pathologies including insulin resistance, dyslipidaemia, hypertension and the genesis of a proinflammatory and prothrombotic environment within individuals is also rapidly increasing, resulting in a condition known as the~metabolic syndrome. From a physiological perspective, one of the most severe consequences of the metabolic syndrome is a progressive inability of the cardiovascular system to adequately perfuse tissues and organs during either elevated metabolic demand and, if sufficiently severe, under basal levels of demand. For the study of the metabolic syndrome, the OZR (obese Zucker rat) represents an important tool in this effort, as the metabolic syndrome in these animals results from a chronic hyperphagia, and thus can be an excellent representation of the human condition. As in afflicted humans, OZR experience an attenuated functional and reactive hyperaemia, and can ultimately experience an ischaemic condition in their skeletal muscles at rest. The source of this progressive ischaemia appears to lie at multiple sites, as endothelium-dependent vasodilator responses are strongly impaired in OZR, and specific constrictor processes (e.g. adrenergic tone) may be enhanced. Whilst these active processes may contribute to a reduction in blood flow under resting conditions or with mild elevations in metabolic demand, an evolving structural alteration to individual microvessels (reduced distensibility) and microvascular networks (reduced microvessel density) also develop and may act to constrain perfusion at higher levels of metabolic demand. Given that constrained muscle perfusion in the metabolic syndrome appears to reflect a highly integrated, multi-faceted effect in OZR, and probably in humans as well, therapeutic interventions must be designed to address each of these contributing elements.

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Year:  2006        PMID: 17144886     DOI: 10.1042/bse0420145

Source DB:  PubMed          Journal:  Essays Biochem        ISSN: 0071-1365            Impact factor:   8.000


  26 in total

1.  Water-soluble rice bran enzymatic extract attenuates dyslipidemia, hypertension and insulin resistance in obese Zucker rats.

Authors:  Maria L Justo; Rosalia Rodriguez-Rodriguez; Carmen M Claro; Maria Alvarez de Sotomayor; Juan Parrado; Maria D Herrera
Journal:  Eur J Nutr       Date:  2012-06-04       Impact factor: 5.614

2.  Type 2 diabetes mellitus in the Goto-Kakizaki rat impairs microvascular function and contributes to premature skeletal muscle fatigue.

Authors:  Jefferson C Frisbee; Matthew T Lewis; Jonathan D Kasper; Paul D Chantler; Robert W Wiseman
Journal:  J Appl Physiol (1985)       Date:  2018-12-20

Review 3.  Control of muscle blood flow during exercise: local factors and integrative mechanisms.

Authors:  I Sarelius; U Pohl
Journal:  Acta Physiol (Oxf)       Date:  2010-03-26       Impact factor: 6.311

4.  Spatial heterogeneity in skeletal muscle microvascular blood flow distribution is increased in the metabolic syndrome.

Authors:  Jefferson C Frisbee; Fan Wu; Adam G Goodwill; Joshua T Butcher; Daniel A Beard
Journal:  Am J Physiol Regul Integr Comp Physiol       Date:  2011-07-20       Impact factor: 3.619

5.  Distinct temporal phases of microvascular rarefaction in skeletal muscle of obese Zucker rats.

Authors:  Jefferson C Frisbee; Adam G Goodwill; Stephanie J Frisbee; Joshua T Butcher; Robert W Brock; I Mark Olfert; Evan R DeVallance; Paul D Chantler
Journal:  Am J Physiol Heart Circ Physiol       Date:  2014-10-10       Impact factor: 4.733

Review 6.  Vascular distribution of nanomaterials.

Authors:  Phoebe A Stapleton; Timothy R Nurkiewicz
Journal:  Wiley Interdiscip Rev Nanomed Nanobiotechnol       Date:  2014-04-28

7.  Transcriptome-wide RNA sequencing analysis of rat skeletal muscle feed arteries. I. Impact of obesity.

Authors:  Nathan T Jenkins; Jaume Padilla; Pamela K Thorne; Jeffrey S Martin; R Scott Rector; J Wade Davis; M Harold Laughlin
Journal:  J Appl Physiol (1985)       Date:  2014-01-16

8.  Increased lipid absorption and transport in the small intestine of zucker obese rats.

Authors:  Keizo Anzai; Koji Fukagawa; Ryuichi Iwakiri; Kazuma Fujimoto; Koichi Akashi; Patrick Tso
Journal:  J Clin Biochem Nutr       Date:  2009-06-30       Impact factor: 3.114

9.  Obesity and vascular dysfunction.

Authors:  Phoebe A Stapleton; Milinda E James; Adam G Goodwill; Jefferson C Frisbee
Journal:  Pathophysiology       Date:  2008-06-20

10.  The prostacyclin analog beraprost sodium ameliorates characteristics of metabolic syndrome in obese Zucker (fatty) rats.

Authors:  Nahoko Sato; Masayuki Kaneko; Mitsutaka Tamura; Hajimu Kurumatani
Journal:  Diabetes       Date:  2010-01-12       Impact factor: 9.461

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