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Acute Inflammation I: Inflammatory Response01:26

Acute Inflammation I: Inflammatory Response

Acute inflammation is a rapid, short-lived physiological response to tissue injury or infection, designed to eliminate harmful agents and initiate repair. This tightly regulated process typically lasts from minutes to several days and is triggered by factors such as microbial invasion, physical trauma, or chemical injury.Recognition and Mediator ReleaseThe inflammatory response begins when resident immune cells—such as mast cells, macrophages, and dendritic cells—detect damage-associated...
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The inflammatory response is the body's defense against infection, injury, or irritation from bacteria, trauma, toxins, or heat. Inflammation helps locate and destroy pathogens and remove damaged tissue elements to heal the body. During this initial phase, fluid, blood products, and nutrients migrate to the injured area, resulting in redness, heat, swelling, ache, and loss of function. Moreover, signs of systemic inflammation include fever, increased WBC count, malaise, anorexia, nausea,...
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Modeling Hypoxia/Reoxygenation Injury in Proximal Tubular Epithelial Cells
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HDL remodeling during the acute phase response.

Anisa Jahangiri1, Maria C de Beer, Victoria Noffsinger

  • 1Department of Internal Medicine, Division of Endocrinology and Molecular Medicine, University of Kentucky, Lexington, KY, USA. anisa.jahangiri@uky.edu

Arteriosclerosis, Thrombosis, and Vascular Biology
|November 15, 2008
PubMed
Summary
This summary is machine-generated.

Serum amyloid A (SAA), secretory phospholipase A(2) (sPLA(2)-IIA), and cholesteryl ester transfer protein (CETP) interact to remodel HDL during the acute phase response, preserving cholesterol efflux capacity.

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Area of Science:

  • Biochemistry
  • Cardiovascular Science
  • Lipid Metabolism

Background:

  • The acute phase (AP) response involves complex changes in plasma proteins.
  • High-density lipoprotein (HDL) undergoes significant remodeling during the AP response.

Purpose of the Study:

  • To investigate the combined effects of SAA, sPLA(2)-IIA, and CETP on HDL remodeling and cholesterol efflux.
  • To understand HDL changes in humans following cardiac surgery during the AP response.

Main Methods:

  • Plasma samples were collected from patients before, and at 1 and 5 days after cardiac surgery.
  • SAA levels, sPLA(2)-IIA activity, and CETP mass and activity were measured.
  • In vitro experiments assessed the impact of SAA, sPLA(2)-IIA, and CETP on HDL remodeling and cholesterol efflux.

Main Results:

  • SAA levels increased 16-fold, and sPLA(2)-IIA activity significantly increased during the AP response.
  • CETP mass and activity decreased, correlating with reduced HDL cholesterol levels.
  • Combined SAA, sPLA(2)-IIA, and CETP markedly remodeled HDL, generating lipid-poor apoA-I and preserving cholesterol efflux capacity.

Conclusions:

  • Complex plasma protein changes during the AP response significantly remodel HDL.
  • This remodeling has functional implications, notably maintaining cholesterol efflux capacity.