PMID- 11715462 OWN - NLM STAT- MEDLINE DCOM- 20020114 LR - 20131121 IS - 0376-2491 (Print) IS - 0376-2491 (Linking) VI - 79 IP - 9 DP - 1999 Sep TI - [The effects of L-arginine and nimodipine on the expression of monocyte chemoattractant protein-1 in endothelial cells induced by lipopolysaccharide]. PG - 699-701 AB - OBJECTIVE: To examine the effects of L-arginine and nimodipine on the expression of monocyte chemoattractant protein-1 (MCP-1) mRNA and protein induced by lipopolysaccharide (LPS) in endothelial cells (ECs). METHODS: After 8-hour exposure to LPS, LPS + L-arginine and LPS + nimodipine respectively, the total RNA in ECs was extracted by the guanidinium isothiocyanate method. The MCP-1 mRNA expression in ECs was examined by Dot blot analysis using a gamma-32P-end-labeled 35 mer oligonucleotide probe of MCP-1. MCP-1 protein in the EC-conditioned media (EC-CM) was determined by sandwich ELISA for each group. The expression of MCP-1 protein in ECs was examined immunocytochemically. RESULTS: Dot blotting showed that after exposure to LPS, the integral absorbance (A) value of the dots of MCP-1 mRNA on the nitrocellulose membrane were 3.14, which was 2.5-fold as much as that in the control group (A = 1.24). The A values of the LPS + L-arginine group and the LPS + nimodipine group were 1.43 and 1.65, respectively. ELISA showed that the MCP-1 protein content in the EC-CM of the LPS group was 6.29 +/- 0.53 ng/ml, which was markedly higher than that of the control group (2.32 +/- 0.16) ng/ml (P < 0.01). The MCP-1 protein content in the EC-CM of the LPS + L-arginine group and the LPS + nimodipine group was significantly lower than that of the LPS group (P < 0.01). Furthermore, the ECs in LPS group showed a strong immunoreactivity for the polyclonal MCP-1 antibody, whereas the ECs in control, L-arginine and nimodipine groups revealed a weak postive immunostaining. CONCLUSION: L-arginine and nimodipine can markedly inhibit the expression of MCP-1 in ECs induced by LPS. FAU - Yu, G AU - Yu G AD - Department of Pathology, Tongji Medical University, Wuhan 430030. FAU - Deng, Z AU - Deng Z LA - chi PT - English Abstract PT - Journal Article PT - Research Support, Non-U.S. Gov't PL - China TA - Zhonghua Yi Xue Za Zhi JT - Zhonghua yi xue za zhi JID - 7511141 RN - 0 (Calcium Channel Blockers) RN - 0 (Chemokine CCL2) RN - 0 (Lipopolysaccharides) RN - 0 (RNA, Messenger) RN - 57WA9QZ5WH (Nimodipine) RN - 94ZLA3W45F (Arginine) SB - IM MH - Animals MH - Aorta, Thoracic/cytology MH - Arginine/*pharmacology MH - Calcium Channel Blockers/*pharmacology MH - Cattle MH - Cells, Cultured MH - Chemokine CCL2/*biosynthesis/genetics MH - Endothelium, Vascular/cytology/*metabolism MH - Lipopolysaccharides/*pharmacology MH - Nimodipine/*pharmacology MH - RNA, Messenger/biosynthesis/genetics EDAT- 2001/11/22 10:00 MHDA- 2002/01/15 10:01 CRDT- 2001/11/22 10:00 PHST- 2001/11/22 10:00 [pubmed] PHST- 2002/01/15 10:01 [medline] PHST- 2001/11/22 10:00 [entrez] PST - ppublish SO - Zhonghua Yi Xue Za Zhi. 1999 Sep;79(9):699-701.