词条 | Pregnane X receptor |
释义 |
In the field of molecular biology, the pregnane X receptor (PXR), also known as the steroid and xenobiotic sensing nuclear receptor (SXR) or nuclear receptor subfamily 1, group I, member 2 (NR1I2) is a protein that in humans is encoded by the NR1I2 (nuclear Receptor subfamily 1, group I, member 2) gene.[1][2][3] FunctionPXR is a nuclear receptor whose primary function is to sense the presence of foreign toxic substances and in response up regulate the expression of proteins involved in the detoxification and clearance of these substances from the body.[4] PXR belongs to the nuclear receptor superfamily, members of which are transcription factors characterized by a ligand-binding domain and a DNA-binding domain. PXR is a transcriptional regulator of the cytochrome P450 gene CYP3A4, binding to the response element of the CYP3A4 promoter as a heterodimer with the 9-cis retinoic acid receptor RXR. It is activated by a range of compounds that induce CYP3A4, including dexamethasone and rifampicin.[3][5] LigandsAgonistsPXR is activated by a large number of endogenous and exogenous chemicals including steroids (e.g., progesterone, 17α-hydroxyprogesterone, 17α-hydroxypregnenolone, 5α-dihydroprogesterone, 5β-dihydroprogesterone, allopregnanolone, corticosterone, cyproterone acetate, spironolactone, dexamethasone, mifepristone), antibiotics (e.g., rifampicin, rifaximin), antimycotics, bile acids, hyperforin (a constituent of the herbal antidepressant St. John's Wort), and many herbal and other compounds (e.g. meclizine, paclitaxel).[4] Cafestol found in coffee is also an agonist.[6] Forskolin is another case example of a PXR agonist.[7][8]AntagonistsKetoconazole is an example of one of the relatively few-known antagonists of the PXR.[9][10] SPA70 (also known as LC-1) was recently identified and characterized as a potent and selective PXR antagonist.[11][12]MechanismLike other type II nuclear receptors, when activated, it forms a heterodimer with the retinoid X receptor, and binds to hormone response elements on DNA which elicits expression of gene products.[4] One of the primary targets of PXR activation is the induction of CYP3A4, an important phase I oxidative enzyme that is responsible for the metabolism of many drugs.[2][3] In addition, PXR up regulates the expression of phase II conjugating enzymes such as glutathione S-transferase[13] and phase III transport uptake and efflux proteins such as OATP2[14] and MDR1.[15][16] See also
References1. ^[https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8856&ordinalpos=1&itool=EntrezSystem2.PEntrez.Gene.Gene_ResultsPanel.Gene_RVDocSum Entrez result for NR1I2]. 2. ^1 {{cite journal | vauthors = Lehmann JM, McKee DD, Watson MA, Willson TM, Moore JT, Kliewer SA | title = The human orphan nuclear receptor PXR is activated by compounds that regulate CYP3A4 gene expression and cause drug interactions | journal = The Journal of Clinical Investigation | volume = 102 | issue = 5 | pages = 1016–23 | date = September 1998 | pmid = 9727070 | pmc = 508967 | doi = 10.1172/JCI3703 }} 3. ^1 2 {{cite journal | vauthors = Bertilsson G, Heidrich J, Svensson K, Asman M, Jendeberg L, Sydow-Bäckman M, Ohlsson R, Postlind H, Blomquist P, Berkenstam A | title = Identification of a human nuclear receptor defines a new signaling pathway for CYP3A induction | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 95 | issue = 21 | pages = 12208–13 | date = October 1998 | pmid = 9770465 | pmc = 22810 | doi = 10.1073/pnas.95.21.12208 | url = http://www.pnas.org/cgi/pmidlookup?view=long&pmid=9770465 }} 4. ^1 2 {{cite journal | vauthors = Kliewer SA, Goodwin B, Willson TM | title = The nuclear pregnane X receptor: a key regulator of xenobiotic metabolism | journal = Endocrine Reviews | volume = 23 | issue = 5 | pages = 687–702 | date = October 2002 | pmid = 12372848 | doi = 10.1210/er.2001-0038 }} 5. ^{{cite web | title = Entrez Gene: NR1I2 nuclear receptor subfamily 1, group I, member 2| url = https://www.ncbi.nlm.nih.gov/sites/entrez?Db=gene&Cmd=ShowDetailView&TermToSearch=8856| access-date = }} 6. ^{{cite journal | vauthors = Ricketts ML, Boekschoten MV, Kreeft AJ, Hooiveld GJ, Moen CJ, Müller M, Frants RR, Kasanmoentalib S, Post SM, Princen HM, Porter JG, Katan MB, Hofker MH, Moore DD | title = The cholesterol-raising factor from coffee beans, cafestol, as an agonist ligand for the farnesoid and pregnane X receptors | journal = Molecular Endocrinology | volume = 21 | issue = 7 | pages = 1603–16 | date = July 2007 | pmid = 17456796 | doi = 10.1210/me.2007-0133 }} 7. ^{{cite journal | vauthors = Kaur J, Sodhi RK, Madan J, Chahal SK, Kumar R | title = Forskolin convalesces memory in high fat diet-induced dementia in wistar rats-Plausible role of pregnane x receptors | journal = Pharmacological Reports | volume = 70 | issue = 1 | pages = 161–171 | date = February 2018 | pmid = 29367103 | doi = 10.1016/j.pharep.2017.07.009 }} 8. ^{{cite journal|last1=Ding|first1=X.|title=Induction of Drug Metabolism by Forskolin: The Role of the Pregnane X Receptor and the Protein Kinase A Signal Transduction Pathway|journal=Journal of Pharmacology and Experimental Therapeutics|volume=312|issue=2|year=2004|pages=849–856|issn=0022-3565|doi=10.1124/jpet.104.076331}} 9. ^{{cite journal | vauthors = Li H, Dou W, Padikkala E, Mani S | title = Reverse yeast two-hybrid system to identify mammalian nuclear receptor residues that interact with ligands and/or antagonists | journal = Journal of Visualized Experiments | volume = | issue = 81 | pages = e51085 | date = November 2013 | pmid = 24300333 | pmc = 3904218 | doi = 10.3791/51085 }} 10. ^{{cite journal | vauthors = Mani S, Dou W, Redinbo MR | title = PXR antagonists and implication in drug metabolism | journal = Drug Metabolism Reviews | volume = 45 | issue = 1 | pages = 60–72 | date = February 2013 | pmid = 23330542 | pmc = 3583015 | doi = 10.3109/03602532.2012.746363 }} 11. ^{{cite journal | vauthors = Lin W, Goktug AN, Wu J, Currier DG, Chen T | title = High-Throughput Screening Identifies 1,4,5-Substituted 1,2,3-Triazole Analogs as Potent and Specific Antagonists of Pregnane X Receptor | journal = Assay and Drug Development Technologies | volume = 15 | issue = 8 | pages = 383–394 | date = December 2017 | pmid = 29112465 | pmc = 5731549 | doi = 10.1089/adt.2017.809 }} 12. ^{{cite journal | vauthors = Lin W, Wang YM, Chai SC, Lv L, Zheng J, Wu J, Zhang Q, Wang YD, Griffin PR, Chen T | title = SPA70 is a potent antagonist of human pregnane X receptor | journal = Nature Communications | volume = 8 | issue = 1 | pages = 741 | date = September 2017 | pmid = 28963450 | pmc = 5622171 | doi = 10.1038/s41467-017-00780-5 }} 13. ^{{cite journal | vauthors = Falkner KC, Pinaire JA, Xiao GH, Geoghegan TE, Prough RA | title = Regulation of the rat glutathione S-transferase A2 gene by glucocorticoids: involvement of both the glucocorticoid and pregnane X receptors | journal = Molecular Pharmacology | volume = 60 | issue = 3 | pages = 611–9 | date = September 2001 | pmid = 11502894 | doi = | url = http://molpharm.aspetjournals.org/cgi/pmidlookup?view=long&pmid=11502894 }} 14. ^{{cite journal | vauthors = Staudinger JL, Goodwin B, Jones SA, Hawkins-Brown D, MacKenzie KI, LaTour A, Liu Y, Klaassen CD, Brown KK, Reinhard J, Willson TM, Koller BH, Kliewer SA | title = The nuclear receptor PXR is a lithocholic acid sensor that protects against liver toxicity | journal = Proceedings of the National Academy of Sciences of the United States of America | volume = 98 | issue = 6 | pages = 3369–74 | date = March 2001 | pmid = 11248085 | pmc = 30660 | doi = 10.1073/pnas.051551698 }} 15. ^{{cite journal | vauthors = Synold TW, Dussault I, Forman BM | title = The orphan nuclear receptor SXR coordinately regulates drug metabolism and efflux | journal = Nature Medicine | volume = 7 | issue = 5 | pages = 584–90 | date = May 2001 | pmid = 11329060 | doi = 10.1038/87912 }} 16. ^{{cite journal | vauthors = Geick A, Eichelbaum M, Burk O | title = Nuclear receptor response elements mediate induction of intestinal MDR1 by rifampin | journal = The Journal of Biological Chemistry | volume = 276 | issue = 18 | pages = 14581–7 | date = May 2001 | pmid = 11297522 | doi = 10.1074/jbc.M010173200 }} Further reading{{refbegin | 2}}
External links
2 : Intracellular receptors|Transcription factors |
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