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Athero-protective properties of plasma lipoproteins from brown bears (URSUS ARCTOS) during hibernation and active state

Pedrelli, M. (author)
Karolinska Institutet, Div Clinical Chemistry, Dep Laboratory Medicine, Huddinge, Sweden; AstraZeneca, Translational Science & Experimental Medicine, Early Cardiovascular, Renal And Metabolism, Biopharmaceuticals R&d, Gothemburg, Sweden
Parini, P. (author)
Karolinska Institutet, Div Clinical Chemistry, Dep Laboratory Medicine, Huddinge, Sweden; Karolinska Institute, Medicine, Stockholm, Sweden; Karolinska University Hospital, Theme Endocrinology And Nephrology, Stockholm, Sweden
Kindberg, J. (author)
Norwegian Institute for Nature Research, Trondheim, Norway; Swedish University of Agricultural Sciences, Department Of Wildlife, Umeå, Sweden
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Arnemo, J. M. (author)
Swedish University of Agricultural Sciences, Department Of Wildlife, Umeå, Sweden; Inland Norway University of Applied Sciences, Dept Of Forestry And Wildlife Management, Koppang, Norway
Björkhem, I. (author)
Karolinska Institutet, Div Clinical Chemistry, Dep Laboratory Medicine, Huddinge, Sweden
Aasa, U. (author)
Umeå universitet, Department Of Community Medicine And Rehabilitation, Umeå, Sweden
Westerstahl, M. (author)
Karolinska Instititet, Div Clinical Physiology, Dept Oflaboratory Medicine, Huddinge, Sweden
Walentinsson, A. (author)
AstraZeneca, Translational Science & Experimental Medicine, Early Cardiovascular, Renal And Metabolism, Biopharmaceuticals R&d, Gothemburg, Sweden
Öörni, K. (author)
Wihuri Research Institute, Atherosclerosis Research Laboratory, Helsinki, Finland
Camejo, G. (author)
Karolinska Institutet, Div Clinical Chemistry, Dep Laboratory Medicine, Huddinge, Sweden
Fröbert, Ole, 1964- (author)
Örebro universitet,Institutionen för medicinska vetenskaper,Department of Cardiology
Hurt-Camejo, E. (author)
Karolinska Institutet, Div Clinical Chemistry, Dep Laboratory Medicine, Huddinge, Sweden; AstraZeneca, Translational Science & Experimental Medicine, Early Cardiovascular, Renal And Metabolism, Biopharmaceuticals R&d, Gothemburg, Sweden
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 (creator_code:org_t)
Elsevier, 2020
2020
English.
In: Atherosclerosis. - : Elsevier. - 0021-9150 .- 1879-1484. ; 315, s. E69-E70
  • Journal article (other academic/artistic)
Abstract Subject headings
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  • Background and Aims: Plasma cholesterol (TC) and triglyceride (TG) levels are twice as high in hibernating brown bears (Ursus arctos) than in healthy humans. Yet, bears display no signs of atherosclerosis. To explore this apparent paradox, lipoprotein structure and function of brown bears were analyzed and compared with those of healthy humans.Methods: Blood from the same wild free-ranging Swedish brown bears (n=10) was drawn during hibernation (winter) and active state (summer). Plasma lipoproteins were separated by size exclusion chromatography, ultracentrifugation and gel-electrophoresis. LDL binding to arterial proteoglycans (PGs) was measured. Data are presented as median (10th - 90th percentile).Results: During hibernation bear LDL carried 4.6 (2.3-5.9) mmol/L cholesterol esters (CE), 1.5 (1.1-2.4) mmol/L unesterified (UC), 3.7 (2.1-4.9) mmol/L TG and 2.5 (1.8-3.4) mmol/L phospholipid (PL). Human LDL were smaller than bear LDL, which were proportionally richer in TG (winter 31 (26-33)%, summer 30 (22-40)%vs human 9% (7-15); p<0.001) and had less CE (winter 36 (26-45)%, summer 25 (21-37)%vs human 48 (46-55)%; p<0.01)). Bear LDL were less positively charged and showed a pre-ß motility on agarose gel. Thus, bear LDL had about 10 times lower binding to PGs than human LDL.Conclusions: Despite high TC and TG levels, bear lipoproteins were less atherogenic than the human analogues. This was due to low LDL affinity for PGs, secondary to increased TG and PL, and to low positive charge. Our study provides further mechanistic insights for the atherosclerosis development, which is driven by the circulating lipoprotein composition and functions rather than plasma absolute lipid levels.

Subject headings

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Kardiologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cardiac and Cardiovascular Systems (hsv//eng)

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