Evidence map›Paper›PMID 39993736›Full record

ArticleJournal of atherosclerosis and thrombosis2025

A Novel ELISA System for Measuring Modified LDL-Adiponectin Complex.

Mai Sasaoka, Akemi Kakino, Roberto Villalobos-Labra, Yuki Yamashita, Floor Spaans, Satoru Joshita, Hiroshi Hosoda, Takeshi Uehara, Chu-Huang Chen, Sandra T Davidge and 1 more

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Article in Journal of atherosclerosis and thrombosis, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Mai SasaokaDepartment of Molecular Pathophysiology, School of Medicine, Shinshu University.
Akemi KakinoDepartment of Molecular Pathophysiology, School of Medicine, Shinshu University.
Roberto Villalobos-LabraDepartment of Obstetrics and Gynecology, University of Alberta.
Yuki YamashitaDepartment of Molecular Pathophysiology, School of Medicine, Shinshu University.
Floor SpaansDepartment of Obstetrics and Gynecology, University of Alberta.
Satoru JoshitaDepartment of Medicine, Division of Gastroenterology and Hepatology, School of Medicine, Shinshu University.
Hiroshi HosodaDepartment of Molecular Pathophysiology, School of Medicine, Shinshu University.
Takeshi UeharaDepartment of Laboratory Medicine, Shinshu University Hospital.
Chu-Huang ChenVascular and Medicinal Research, The Texas Heart Institute.
Sandra T DavidgeDepartment of Obstetrics and Gynecology, University of Alberta.
Tatsuya SawamuraDepartment of Molecular Pathophysiology, School of Medicine, Shinshu University.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimAdiponectin is an anti-diabetic and anti-atherogenic protein secreted primarily from adipose tissue. Adiponectin and modified LDL (mLDL) form a complex to modulate their biological activity. To elucidate the significance of the complex formation, we analyzed its effects on vascular tissue and developed and verified novel quantifying methods for adiponectin.

methodsTo study the significance of the mLDL-adiponectin complex (MAC) formation, we used the wire-myography method on rat mesenteric artery. We developed a method to measure MAC by using LOX-1 as the capture protein and anti-adiponectin antibody for detection. We compared serum MAC levels between hemodialysis patients and control subjects.

resultsAdministering mLDL alone to rat mesenteric artery impaired endothelium-dependent vasorelaxation, whereas simultaneously administering adiponectin with mLDL protected rat mesenteric artery from the mLDL-induced impairment of vasorelaxation. This finding indicates MAC formation prevents endothelium from mLDL-induced dysfunction in tissue. Using our novel ELISA for MAC, we found that MAC was increasingly detectable depending on the doses of mLDL and adiponectin in vitro. In serum, hemodialysis patients showed a significantly higher ratio of MAC-high patients (higher than the median level of MAC) than did healthy controls. Furthermore, the MAC-high hemodialysis group had lower mLDL activity measured as LOX-1 ligand containing apoB.

conclusionUsing our ELISA, we detected MAC in human serum that protected blood vessels from the deleterious effects of oxidized LDL.

Indexed as

AdiponectinLipoproteins, LDLAgedAnimalsCase-Control StudiesEndothelium, VascularEnzyme-Linked Immunosorbent AssayFemaleHumansMaleMesenteric ArteriesMiddle AgedRatsRenal DialysisScavenger Receptors, Class EAdiponectinLipoproteins, LDLoxidized low density lipoproteinScavenger Receptors, Class EAdiponectinLOX-1Modified LDLModified LDL-adiponectin complex

Identifiers

PMID39993736
PMCPMC12416962

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