New use of benserazide hydrochloride reverse cholesterol transport way
A technology of benserazide hydrochloride and cholesterol, which is applied in the field of biomedicine and can solve problems such as hepatic high-density lipoprotein cholesterol uptake blockage
Patent Information
- Authority / Receiving Office
- CN · China
- Current Assignee / Owner
- Publication Date
- 2016-01-27
- Estimated Expiration
- Not applicable · inactive patent
Smart Images
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Abstract
Description
Technical field
[0001] The present invention relates to the field of biomedicine, and mainly relates to the effect of benserazide hydrochloride on the expression of two important rate-limiting receptors of the reverse cholesterol transport pathway (RCT), thereby promoting the reverse cholesterol transport pathway (RCT) to reverse atherosclerosis . Background technique
[0002] Atherosclerosis (AS) has become an important cause of human death. Among them, it is generally believed that high-density lipoprotein (HDL) has the effect of inhibiting atherosclerosis, mainly through its mediated reverse cholesterol transport pathway (RCT). to realise.
[0003] The reverse cholesterol transport pathway (RCT) mainly promotes cholesterol efflux from macrophages through a variety of ways, and promotes lipidation of ApoA-1 and HDL, and then mature HDL is transported to the liver for excretion and secretion, thereby hindering atherosclerosis. The ATP-binding cassette transporter A1 (ABCA1) is m...
Examples
Embodiment Construction
[0023] 1) Cells stained with Oil Red O are washed with PBS→fixed with 4% paraformaldehyde for 10~20min-→washed with PBS→stained with Oil Red O for 15min→washed with water→observed under microscope
[0024] 2) cell-basedELISA detection
[0025] After the cells are incubated for 24 hours, discard the culture medium, wash and dry, fix the cells with 4% paraformaldehyde for 20-30 minutes, rinse with PBS / TritonX-100 for 5 minutes × 3 times, 0.6% H 2 O 2 Incubate with PBS / Tritonx-100 for 20-30min to block endogenous peroxidase, rinse with PBS / TritonX-100 for 5min×3 times, block with 10% BSA at 37°C for 1h40min, and incubate with 50u15% BSA diluted SRB1 primary antibody at 4°C Overnight, rinse with PBS / TritonX-100 for 5min×3 times, incubate with 50ul 5% BSA diluted horseradish peroxidase labeled secondary antibody at 37℃ for 1h, rinse with PBS / TritonX-100 for 5min×3 times, rinse with PBS for 5min×3 times, Add 200ul TMB color developing solution to each well and keep it at 37°C for 30 minu...