2013HeartRequires access

GW24-e1903 Effect of ox-LDL and atorvastatin on the production of interleukin-18 in and the proliferation of cultured human umbilical vein endothelial cells

Aiqin Zhou, Xiaoping Wang

Open publisher page 0 citations

Abstract

Objectives To investigate the effects of atorvastatin on the production of interleukin-18(IL18) in and the proliferation of cultured human umbilical vein endothelial cells (HUVECs) activated by oxidised low density lipoprotein (Ox-LDL). Methods HUVECs Cultured in vitro at passage 3 to 9 were used for experiment. There were three groups: 1) control group; 2) Ox-LDL groups (100 mg/L); 3) Ox-LDL + atorvastatin groups: cells were firstly incubated with 0.01, 0.05, 0.1, 0.5, 1 µmol/L atorvastatin respectively for 4 h,then incubated with 100 mg/L Ox-LDL for 24 h. IL18 in supernatant medium was detected by cell ELISA and cell proliferation was measured by MTT colorimetric assay. Results Compared with control group,ox-LDL (100 mg/L) could inhibit the proliferation of HUVECs (P < 0.01). Atorvastatin could dose-dependently enhance the proliferation of HUVECs activated by Ox-LDL (P < 0.05, P < 0.01). HUVECs didn’t release IL18 without stimulation. ox-LDL(100 mg/L) stimulated the production of IL18 by HUVECs. Atorvastatin (0.05, 0.1, 0.5, 1 µmol/L) could inhibit the production of IL18 in HUVECs activated by Ox-LDL (P < 0.05, P < 0.01), but not in 0.01 µmol/L (P < 0.05). The inhibitory effect was dose-dependent. Conclusions atorvastatin can obviously inhibited the production of IL18 in HUVECs and enhanced the proliferation of HUVECs activated by Ox-LDL, which might improve the impaired endothelial cell beyond lipid regulation function.

About this research paper

What this paper is about

Objectives To investigate the effects of atorvastatin on the production of interleukin-18(IL18) in and the proliferation of cultured human umbilical vein endothelial cells (HUVECs) activated by oxidised low density lipoprotein (Ox-LDL). Methods HUVECs Cultured in vitro at passage 3 to 9 were used for experiment. There were three groups: 1) control group; 2) Ox-LDL groups (100 mg/L); 3) Ox-LDL + atorvastatin groups: cells were firstly incubated with 0.01, 0.05, 0.1, 0.5, 1 µmol/L atorvastatin respectively for 4 h,then incubated with 100 mg/L Ox-LDL for 24 h. IL18 in supernatant medium was detected by cell ELISA and cell proliferation was measured by MTT colorimetric assay. Results Compared with control group,ox-LDL (100 mg/L) could inhibit the proliferation of HUVECs (P < 0.01). Atorvastatin could dose-dependently enhance the proliferation of HUVECs activated by Ox-LDL (P < 0.05, P < 0.01). HUVECs didn’t release IL18 without stimulation. ox-LDL(100 mg/L) stimulated the production of IL18 by HUVECs. Atorvastatin (0.05, 0.1, 0.5, 1 µmol/L) could inhibit the production of IL18 in HUVECs activated by Ox-LDL (P < 0.05, P < 0.01), but not in 0.01 µmol/L (P < 0.05). The inhibitory effect was dose-dependent. Conclusions atorvastatin can obviously inhibited the production of IL18 in HUVECs and enhanced the proliferation of HUVECs activated by Ox-LDL, which might improve the impaired endothelial cell beyond lipid regulation function.

Why it matters

A significance statement is not available in the OpenAlex record.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Available abstract

Objectives To investigate the effects of atorvastatin on the production of interleukin-18(IL18) in and the proliferation of cultured human umbilical vein endothelial cells (HUVECs) activated by oxidised low density lipoprotein (Ox-LDL). Methods HUVECs Cultured in vitro at passage 3 to 9 were used for experiment. There were three groups: 1) control group; 2) Ox-LDL groups (100 mg/L); 3) Ox-LDL + atorvastatin groups: cells were firstly incubated with 0.01, 0.05, 0.1, 0.5, 1 µmol/L atorvastatin respectively for 4 h,then incubated with 100 mg/L Ox-LDL for 24 h. IL18 in supernatant medium was detected by cell ELISA and cell proliferation was measured by MTT colorimetric assay. Results Compared with control group,ox-LDL (100 mg/L) could inhibit the proliferation of HUVECs (P < 0.01). Atorvastatin could dose-dependently enhance the proliferation of HUVECs activated by Ox-LDL (P < 0.05, P < 0.01). HUVECs didn’t release IL18 without stimulation. ox-LDL(100 mg/L) stimulated the production of IL18 by HUVECs. Atorvastatin (0.05, 0.1, 0.5, 1 µmol/L) could inhibit the production of IL18 in HUVECs activated by Ox-LDL (P < 0.05, P < 0.01), but not in 0.01 µmol/L (P < 0.05). The inhibitory effect was dose-dependent. Conclusions atorvastatin can obviously inhibited the production of IL18 in HUVECs and enhanced the proliferation of HUVECs activated by Ox-LDL, which might improve the impaired endothelial cell beyond lipid regulation function.

Key concepts: Atorvastatin, Umbilical vein, Medicine, Cell growth, Interleukin 18, Interleukin, In vitro, Molecular biology

Related papers

Back to paper searchBrowse research topicsOriginal source
GW24-e1903 Effect of ox-LDL and atorvastatin on the production of interleukin-18 in and the proliferation of cultured human umbilical vein endothelial cells — Research Paper | ScholarLens