Arginin vazopresinski receptor 2

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Identifikatori
Simboli AVPR2; ADHR; DI1; DIR; DIR3; MGC126533; MGC138386; NDI; V2R
Vanjski ID OMIM300538 MGI88123 HomoloGene20064 IUPHAR: V2 GeneCards: AVPR2 Gene
Ortolozi
Vrsta Čovek Miš
Entrez 554 12000
Ensembl ENSG00000126895 ENSMUSG00000031390
UniProt P30518 Q3KNZ4
RefSeq (mRNA) NM_000054 NM_019404
RefSeq (protein) NP_000045 NP_062277
Lokacija (UCSC) Chr X:
152.82 - 152.83 Mb
Chr X:
70.13 - 70.15 Mb
PubMed pretraga [1] [2]

Arginin vazopresinski receptor 2 (AVPR2) je protein koji deluje receptor za arginin vazopresin.[1] AVPR2 pripada familiji G protein-spregnutih receptora. Njegovo dejstvo je posredovano Gs tipom G proteina, koji stimuliše adenilat ciklazu.

Antagonisti[уреди]

Selektivni antagonisti vazopresinskog receptora su:

Njihova glavna upotreba je lečenje hiponatremije, koja može da bude izazvana sindromom neodgovarajućeg izlučivanja antidiuretskog hormona (SIADH) i cirozom.

Interakcije[уреди]

Za arginin vazopresinski receptor 2 je bilo pokazano da interaguje sa C1QTNF1.[2]

Reference[уреди]

  1. ^ van den Ouweland AM, Knoop MT, Knoers VV, Markslag PW, Rocchi M, Warren ST, Ropers HH, Fahrenholz F, Monnens LA, van Oost BA (1992). „Colocalization of the gene for nephrogenic diabetes insipidus (DIR) and the vasopressin type 2 receptor gene (AVPR2) in the Xq28 region”. Genomics. 13 (4): 1350—2. PMID 1324225. doi:10.1016/0888-7543(92)90067-3. 
  2. ^ Innamorati, Giulio; Whang Michael Insuk; Molteni Raffaella; Le Gouill Christian; Birnbaumer Mariel (2002). „GIP, a G-protein-coupled receptor interacting protein”. Regul. Pept. Netherlands. 109 (1–3): 173—9. ISSN 0167-0115. PMID 12409230. doi:10.1016/S0167-0115(02)00201-X.  Проверите вредност парамет(а)ра за датум: |date= (помоћ)

Literatura[уреди]

  • Birnbaumer M (2001). „The V2 vasopressin receptor mutations and fluid homeostasis”. Cardiovasc. Res. 51 (3): 409—15. PMID 11476731. doi:10.1016/S0008-6363(01)00337-6. 
  • Ishikawa SE (2002). „[Nephrogenic diabetes insipidus associated with mutations of vasopressin V2 receptors and aquaporin-2]”. Nippon Rinsho. 60 (2): 350—5. PMID 11857925. 
  • Thibonnier M, Coles P, Thibonnier A, Shoham M (2002). „Molecular pharmacology and modeling of vasopressin receptors”. Prog. Brain Res. 139: 179—96. PMID 12436935. doi:10.1016/S0079-6123(02)39016-2. 
  • Bichet DG (2006). „Nephrogenic diabetes insipidus”. Advances in chronic kidney disease. 13 (2): 96—104. PMID 16580609. doi:10.1053/j.ackd.2006.01.006. 
  • Robben JH, Knoers NV, Deen PM (2006). „Cell biological aspects of the vasopressin type-2 receptor and aquaporin 2 water channel in nephrogenic diabetes insipidus”. Am. J. Physiol. Renal Physiol. 291 (2): F257—70. PMID 16825342. doi:10.1152/ajprenal.00491.2005. 
  • Pan Y; Metzenberg A; Das S; et al. (1993). „Mutations in the V2 vasopressin receptor gene are associated with X-linked nephrogenic diabetes insipidus”. Nat. Genet. 2 (2): 103—6. PMID 1303257. doi:10.1038/ng1092-103. 
  • van den Ouweland AM; Dreesen JC; Verdijk M; et al. (1993). „Mutations in the vasopressin type 2 receptor gene (AVPR2) associated with nephrogenic diabetes insipidus”. Nat. Genet. 2 (2): 99—102. PMID 1303271. doi:10.1038/ng1092-99. 
  • van den Ouweland AM; Knoop MT; Knoers VV; et al. (1992). „Colocalization of the gene for nephrogenic diabetes insipidus (DIR) and the vasopressin type 2 receptor gene (AVPR2) in the Xq28 region”. Genomics. 13 (4): 1350—2. PMID 1324225. doi:10.1016/0888-7543(92)90067-3. 
  • Rosenthal W; Seibold A; Antaramian A; et al. (1992). „Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidus”. Nature. 359 (6392): 233—5. PMID 1356229. doi:10.1038/359233a0. 
  • Seibold A, Brabet P, Rosenthal W, Birnbaumer M (1992). „Structure and chromosomal localization of the human antidiuretic hormone receptor gene”. Am. J. Hum. Genet. 51 (5): 1078—83. PMC 1682836Слободан приступ. PMID 1415251. 
  • Birnbaumer M; Seibold A; Gilbert S; et al. (1992). „Molecular cloning of the receptor for human antidiuretic hormone”. Nature. 357 (6376): 333—5. PMID 1534149. doi:10.1038/357333a0. 
  • Lolait SJ; O'Carroll AM; McBride OW; et al. (1992). „Cloning and characterization of a vasopressin V2 receptor and possible link to nephrogenic diabetes insipidus”. Nature. 357 (6376): 336—9. PMID 1534150. doi:10.1038/357336a0. 
  • Knoers N; van der Heyden H; van Oost BA; et al. (1989). „Three-point linkage analysis using multiple DNA polymorphic markers in families with X-linked nephrogenic diabetes insipidus”. Genomics. 4 (3): 434—7. PMID 2714800. doi:10.1016/0888-7543(89)90352-2. 
  • Tsukaguchi H; Matsubara H; Taketani S; et al. (1995). „Binding-, intracellular transport-, and biosynthesis-defective mutants of vasopressin type 2 receptor in patients with X-linked nephrogenic diabetes insipidus”. J. Clin. Invest. 96 (4): 2043—50. PMC 185843Слободан приступ. PMID 7560098. doi:10.1172/JCI118252. 
  • Faà V; Ventruto ML; Loche S; et al. (1995). „Mutations in the vasopressin V2-receptor gene in three families of Italian descent with nephrogenic diabetes insipidus”. Hum. Mol. Genet. 3 (9): 1685—6. PMID 7833930. doi:10.1093/hmg/3.9.1685. 
  • Birnbaumer M, Gilbert S, Rosenthal W (1995). „An extracellular congenital nephrogenic diabetes insipidus mutation of the vasopressin receptor reduces cell surface expression, affinity for ligand, and coupling to the Gs/adenylyl cyclase system”. Mol. Endocrinol. 8 (7): 886—94. PMID 7984150. doi:10.1210/me.8.7.886. 
  • Wenkert D; Merendino JJ; Shenker A; et al. (1995). „Novel mutations in the V2 vasopressin receptor gene of patients with X-linked nephrogenic diabetes insipidus”. Hum. Mol. Genet. 3 (8): 1429—30. PMID 7987330. doi:10.1093/hmg/3.8.1429. 
  • Oksche A; Dickson J; Schülein R; et al. (1995). „Two novel mutations in the vasopressin V2 receptor gene in patients with congenital nephrogenic diabetes insipidus”. Biochem. Biophys. Res. Commun. 205 (1): 552—7. PMID 7999078. doi:10.1006/bbrc.1994.2700. 
  • Bichet DG; Birnbaumer M; Lonergan M; et al. (1994). „Nature and recurrence of AVPR2 mutations in X-linked nephrogenic diabetes insipidus”. Am. J. Hum. Genet. 55 (2): 278—86. PMC 1918376Слободан приступ. PMID 8037205. 
  • Yuasa H; Ito M; Oiso Y; et al. (1994). „Novel mutations in the V2 vasopressin receptor gene in two pedigrees with congenital nephrogenic diabetes insipidus”. J. Clin. Endocrinol. Metab. 79 (2): 361—5. PMID 8045948. doi:10.1210/jc.79.2.361. 

Spoljašnje veze[уреди]