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

被引:32
作者
Hamakawa, Y
Omori, N
Ouchida, M
Nagase, M
Sato, K
Nagano, I
Shoji, M
Fujita, T
Abe, K
机构
[1] Okayama Univ, Grad Sch Med & Dent, Dept Neurol, Okayama 7008558, Japan
[2] Okayama Univ, Grad Sch Med & Dent, Dept Mol Genet, Okayama 7008558, Japan
[3] Univ Tokyo, Sch Med, Dept Internal Med, Tokyo 112, Japan
关键词
atherosclerosis; common carotid artery; LOX-1; MCP-1; SHR-SP;
D O I
10.1179/016164104225016074
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Lectin-like oxidized low-density lipoprotein receptor (LOX-1) and monocyte chemoattractant protein- I (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.
引用
收藏
页码:767 / 773
页数:7
相关论文
共 34 条
[1]   ISCHEMIC DELAYED NEURONAL DEATH - A MITOCHONDRIAL HYPOTHESIS [J].
ABE, K ;
AOKI, M ;
KAWAGOE, J ;
YOSHIDA, T ;
HATTORI, A ;
KOGURE, K ;
ITOYAMA, Y .
STROKE, 1995, 26 (08) :1478-1489
[2]   SELECTIVE INDUCTION OF KUNITZ-TYPE PROTEASE INHIBITOR DOMAIN-CONTAINING AMYLOID PRECURSOR PROTEIN MESSENGER-RNA AFTER PERSISTENT FOCAL ISCHEMIA IN RAT CEREBRAL-CORTEX [J].
ABE, K ;
TANZI, RE ;
KOGURE, K .
NEUROSCIENCE LETTERS, 1991, 125 (02) :172-174
[3]   Decreased lesion formation in CCR2-/- mice reveals a role for chemokines in the initiation of atherosclerosis [J].
Boring, L ;
Gosling, J ;
Cleary, M ;
Charo, IF .
NATURE, 1998, 394 (6696) :894-897
[4]   Increased expression of lectinlike oxidized low density lipoprotein receptor-1 in initial atherosclerotic lesions of Watanabe heritable hyperlipidemic rabbits [J].
Chen, MY ;
Kakutani, M ;
Minami, M ;
Kataoka, H ;
Kume, N ;
Narumiya, S ;
Kita, T ;
Masaki, T ;
Sawamura, T .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 2000, 20 (04) :1107-1115
[5]   Effects of an angiotensin-converting enzyme inhibitor and a β-blocker on cerebral arteriolar dilatation in hypertensive rats [J].
Chillon, JM ;
Baumbach, GL .
HYPERTENSION, 2001, 37 (06) :1388-1393
[6]   Absence of monocyte chemoattractant protein-1 reduces atherosclerosis in low density lipoprotein receptor-deficient mice [J].
Gu, L ;
Okada, Y ;
Clinton, SK ;
Gerard, C ;
Sukhova, GK ;
Libby, P ;
Rollins, BJ .
MOLECULAR CELL, 1998, 2 (02) :275-281
[7]   INDIRECT SYSTOLIC AND MEAN BLOOD-PRESSURE DETERMINATION BY A NEW TAIL CUFF METHOD IN SPONTANEOUSLY HYPERTENSIVE RATS [J].
IKEDA, K ;
NARA, Y ;
YAMORI, Y .
LABORATORY ANIMALS, 1991, 25 (01) :26-29
[8]   Nitric oxide deficiency induces myocardial infarction in hypercholesterolaemic stroke-prone spontaneously hypertensive rats [J].
Ikeda, K ;
Nara, Y ;
Tagami, M ;
Yamori, Y .
CLINICAL AND EXPERIMENTAL PHARMACOLOGY AND PHYSIOLOGY, 1997, 24 (05) :344-348
[9]   Expression of lectinlike oxidized low-density lipoprotein receptor-1 in human atherosclerotic lesions [J].
Kataoka, H ;
Kume, N ;
Miyamoto, S ;
Minami, M ;
Moriwaki, H ;
Murase, T ;
Sawamura, T ;
Masaki, T ;
Hashimoto, N ;
Kita, T .
CIRCULATION, 1999, 99 (24) :3110-3117
[10]   LOX-1, a possible clue to the missing link between hypertension and atherogenesis [J].
Kita, T .
CIRCULATION RESEARCH, 1999, 84 (09) :1113-1115