Publication: Potential role of lycopene in targeting proprotein convertase subtilisin/kexin type-9 to combat hypercholesterolemia
dc.contributor.author | Alvi, Sahir Sultan | |
dc.contributor.author | Ansari, Irfan A. | |
dc.contributor.author | Khan, IMRAN | |
dc.contributor.author | Iqbal, Johar | |
dc.contributor.author | Khan, M. Salman | |
dc.contributor.institutionauthor | KHAN, IMRAN | |
dc.date.accessioned | 2021-04-10T20:59:09Z | |
dc.date.available | 2021-04-10T20:59:09Z | |
dc.date.issued | 2017-07-01T00:00:00Z | |
dc.description.abstract | Proprotein convertase subtilisin/kexin type 9 (PCSK-9) is a serine protease of the proprotien convertase (PC) family that has profound effects on plasma low density lipoprotein cholesterol (LDL-C) levels, the major risk factor for coronary heart disease (CHD), through its ability to mediate LDL receptor (LDL-R) protein degradation and reduced recycling to the surface of hepatocytes. Thus, the current study was premeditated not only to evaluate the role of lycopene in targeting the inhibition of PCSK-9 via modulation of genes involved in cholesterol homeostasis in HFD rats but also to examine a correlation between HFD induced inflammatory cascades and subsequent regulation of PCSK-9 expression. Besides the effect of lycopene on hepatic PCSK-9 gene expression, PPI studies for PCSK-9-Lycopene complex and EGF-A of LDL-R were also performed via molecular informatics approach to assess the dual mode of action of lycopene in LDL-R recycling and increased removal of circulatory LDL-C. We for the first time deciphered that lycopene treatment significantly down-regulates the expression of hepatic PCSK-9 and HMGR, whereas, hepatic LDL-R expression was significantly up-regulated. Furthermore, lycopene ameliorated inflammation stimulated expression of PCSK-9 via suppressing the expression of inflammatory markers. The results from our molecular informatics studies confirmed that lycopene, while occupying the active site of PCSK-9 crystal structure, reduces the affinity of PCSK-9 to complex with EGF-A of LDL-R, whereas, atorvastatin makes PCSK-9-EGF-A complex formation more feasible than both of PCSK-9-EGF-A alone and Lycopene-PCSK-9-EGF-A complex. Based on above results, it can be concluded that lycopene exhibits potent hypolipidemic activities via molecular mechanisms that are either identical (HMGR inhibition) or distinct from that of statins (down-regulation of PCSK-9 mRNA synthesis). To the best of our knowledge, this is the first report that lycopene has this specific biological property. Being a natural, safer and alternative therapeutic agent, lycopene could be used as a complete regulator of cholesterol homeostasis and ASCVD. | |
dc.identifier.citation | Alvi S. S. , Ansari I. A. , Khan I., Iqbal J., Khan M. S. , -Potential role of lycopene in targeting proprotein convertase subtilisin/kexin type-9 to combat hypercholesterolemia-, FREE RADICAL BIOLOGY AND MEDICINE, cilt.108, ss.394-403, 2017 | |
dc.identifier.doi | 10.1016/j.freeradbiomed.2017.04.012 | |
dc.identifier.scopus | 85017535559 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12645/28723 | |
dc.identifier.wos | WOS:000403463500036 | |
dc.title | Potential role of lycopene in targeting proprotein convertase subtilisin/kexin type-9 to combat hypercholesterolemia | |
dc.type | Article | |
dspace.entity.type | Publication | |
local.avesis.id | 86e8fd4f-6426-4617-abd6-e5c5ecdad66a | |
local.indexed.at | WOS | |
local.indexed.at | Scopus | |
local.publication.isinternational | 1 | |
relation.isAuthorOfPublication | 096be806-cf26-4766-b5b4-26f30c593af2 | |
relation.isAuthorOfPublication.latestForDiscovery | 096be806-cf26-4766-b5b4-26f30c593af2 |