Severity dependent up-regulations of LOX-1 and MCP-1 in early sclerotic changes of common carotid arteries in spontaneously hypertensive rats

Neurol Res. 2004 Oct;26(7):767-73. doi: 10.1179/016164104225016074.

Abstract

Lectin-like oxidized low-density lipoprotein receptor (LOX-1) and monocyte chemoattractant protein-1 (MCP-1) are molecules involving in the initiation and progression of atherosclerosis. In order to examine a possible difference in LOX-1 and MCP-1 expressions depending on the severity of early stage of atherosclerosis, we investigated atherosclerotic changes by exposure to hypertension and hyperlipidemia in common carotid arteries (CCAs) of stroke-prone spontaneously hypertensive rat (SHR-SP). Three rat model groups such as control [Wistar Kyoto rat (WKY) group], hypertension (SHR-SP group) and hypertension + hyperlipidemia [SHR-SP + high fat and cholesterol (HFC) group] were used. Body weights, brain weights, systolic blood pressures and serum levels of total cholesterol, low-density lipoprotein and triglyceride were measured at 0, 5, 10 and 15 days after appropriate diet. Immunohistochemistry showed that the positive area and the strength of LOX-1 and MCP-1 were larger in the SHR-SP + HFC group than in the SHR-SP group, while no immunoreactivities were found in the WKY group. Conventional RT-PCR and real-time PCR analyses showed that mRNAs of those in the SHR-SP group were higher with greater up-regulation in the SHR-SP + HFC group. LOX-1 and MCP-1 expressions were coordinately up-regulated at mRNA and protein levels in an early stage of sclerosis depending on the severity of atherosclerotic stress. Activations of LOX-1 and MCP-1 are collectively involved in the early stage of atherosclerosis.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Arteriosclerosis / etiology
  • Arteriosclerosis / metabolism*
  • Biomarkers / metabolism
  • Body Weight / physiology
  • Brain / physiology
  • Carotid Artery, Common / metabolism*
  • Chemokine CCL2 / genetics
  • Chemokine CCL2 / metabolism*
  • Diet
  • Hypertension / genetics
  • Hypertension / pathology*
  • Immunohistochemistry / methods
  • Lipids / blood
  • Male
  • Models, Cardiovascular
  • Organ Size
  • RNA, Messenger / biosynthesis
  • Rats
  • Rats, Inbred SHR
  • Rats, Inbred WKY
  • Receptors, LDL / genetics
  • Receptors, LDL / metabolism*
  • Receptors, Oxidized LDL
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Scavenger Receptors, Class E
  • Time Factors
  • Up-Regulation

Substances

  • Biomarkers
  • Ccl2 protein, rat
  • Chemokine CCL2
  • Lipids
  • OLR1 protein, rat
  • RNA, Messenger
  • Receptors, LDL
  • Receptors, Oxidized LDL
  • Scavenger Receptors, Class E