172 related articles for article (PubMed ID: 16399693)
1. The full expression of fasting-induced torpor requires beta 3-adrenergic receptor signaling.
Swoap SJ; Gutilla MJ; Liles LC; Smith RO; Weinshenker D
J Neurosci; 2006 Jan; 26(1):241-5. PubMed ID: 16399693
[TBL] [Abstract][Full Text] [Related]
2. Norepinephrine controls both torpor initiation and emergence via distinct mechanisms in the mouse.
Swoap SJ; Weinshenker D
PLoS One; 2008; 3(12):e4038. PubMed ID: 19107190
[TBL] [Abstract][Full Text] [Related]
3. Selective activation of beta3-adrenoceptors by octopamine: comparative studies in mammalian fat cells.
Carpéné C; Galitzky J; Fontana E; Atgié C; Lafontan M; Berlan M
Naunyn Schmiedebergs Arch Pharmacol; 1999 Apr; 359(4):310-21. PubMed ID: 10344530
[TBL] [Abstract][Full Text] [Related]
4. Activation of beta2- and beta3-adrenergic receptors increases brain tryptophan.
Lenard NR; Gettys TW; Dunn AJ
J Pharmacol Exp Ther; 2003 May; 305(2):653-9. PubMed ID: 12606631
[TBL] [Abstract][Full Text] [Related]
5. Norepinephrine is required for leptin effects on gene expression in brown and white adipose tissue.
Commins SP; Marsh DJ; Thomas SA; Watson PM; Padgett MA; Palmiter R; Gettys TW
Endocrinology; 1999 Oct; 140(10):4772-8. PubMed ID: 10499537
[TBL] [Abstract][Full Text] [Related]
6. Peripheral ghrelin deepens torpor bouts in mice through the arcuate nucleus neuropeptide Y signaling pathway.
Gluck EF; Stephens N; Swoap SJ
Am J Physiol Regul Integr Comp Physiol; 2006 Nov; 291(5):R1303-9. PubMed ID: 16825418
[TBL] [Abstract][Full Text] [Related]
7. Deletion of Nhlh2 results in a defective torpor response and reduced Beta adrenergic receptor expression in adipose tissue.
Wankhade UD; Vella KR; Fox DL; Good DJ
PLoS One; 2010 Aug; 5(8):e12324. PubMed ID: 20808804
[TBL] [Abstract][Full Text] [Related]
8. Induction of beta3-adrenergic receptor functional expression following chronic stimulation with noradrenaline in neonatal rat cardiomyocytes.
Germack R; Dickenson JM
J Pharmacol Exp Ther; 2006 Jan; 316(1):392-402. PubMed ID: 16183708
[TBL] [Abstract][Full Text] [Related]
9. Activation of beta(3) adrenergic receptors suppresses leptin expression and mediates a leptin-independent inhibition of food intake in mice.
Mantzoros CS; Qu D; Frederich RC; Susulic VS; Lowell BB; Maratos-Flier E; Flier JS
Diabetes; 1996 Jul; 45(7):909-14. PubMed ID: 8666142
[TBL] [Abstract][Full Text] [Related]
10. Role of alpha-adrenergic receptors in the effect of the beta-adrenergic receptor ligands, CGP 12177, bupranolol, and SR 59230A, on the contraction of rat intrapulmonary artery.
Leblais V; Pourageaud F; Ivorra MD; Guibert C; Marthan R; Muller B
J Pharmacol Exp Ther; 2004 Apr; 309(1):137-45. PubMed ID: 14718590
[TBL] [Abstract][Full Text] [Related]
11. Mice with chronic norepinephrine deficiency resemble amphetamine-sensitized animals.
Weinshenker D; Miller NS; Blizinsky K; Laughlin ML; Palmiter RD
Proc Natl Acad Sci U S A; 2002 Oct; 99(21):13873-7. PubMed ID: 12370425
[TBL] [Abstract][Full Text] [Related]
12. beta3-Adrenergic-dependent and -independent mechanisms participate in cold-induced modulation of insulin signal transduction in brown adipose tissue of rats.
Gasparetti AL; Alvarez-Rojas F; de Araujo EP; Hirata AE; Saad MJ; Velloso LA
Pflugers Arch; 2005 Mar; 449(6):537-46. PubMed ID: 15750837
[TBL] [Abstract][Full Text] [Related]
13. Central adenosine receptor signaling is necessary for daily torpor in mice.
Iliff BW; Swoap SJ
Am J Physiol Regul Integr Comp Physiol; 2012 Sep; 303(5):R477-84. PubMed ID: 22785425
[TBL] [Abstract][Full Text] [Related]
14. An increase in murine skeletal muscle peroxisome proliferator-activated receptor-gamma coactivator-1alpha (PGC-1alpha) mRNA in response to exercise is mediated by beta-adrenergic receptor activation.
Miura S; Kawanaka K; Kai Y; Tamura M; Goto M; Shiuchi T; Minokoshi Y; Ezaki O
Endocrinology; 2007 Jul; 148(7):3441-8. PubMed ID: 17446185
[TBL] [Abstract][Full Text] [Related]
15. Analysis of brain adrenergic receptors in dopamine-beta-hydroxylase knockout mice.
Sanders JD; Szot P; Weinshenker D; Happe HK; Bylund DB; Murrin LC
Brain Res; 2006 Sep; 1109(1):45-53. PubMed ID: 16854392
[TBL] [Abstract][Full Text] [Related]
16. Norepinephrine induces hepatic fibrogenesis in leptin deficient ob/ob mice.
Oben JA; Roskams T; Yang S; Lin H; Sinelli N; Li Z; Torbenson M; Thomas SA; Diehl AM
Biochem Biophys Res Commun; 2003 Aug; 308(2):284-92. PubMed ID: 12901866
[TBL] [Abstract][Full Text] [Related]
17. Evidence for pleiotropic signaling at the mouse beta3-adrenoceptor revealed by SR59230A [3-(2-Ethylphenoxy)-1-[(1,S)-1,2,3,4-tetrahydronapth-1-ylamino]-2S-2-propanol oxalate].
Hutchinson DS; Sato M; Evans BA; Christopoulos A; Summers RJ
J Pharmacol Exp Ther; 2005 Mar; 312(3):1064-74. PubMed ID: 15574684
[TBL] [Abstract][Full Text] [Related]
18. Differential regulation of beta3-adrenoceptors in gut and adipose tissue of genetically obese (ob/ob) C57BL/6J-mice.
Evans BA; Papaioannou M; Anastasopoulos F; Summers RJ
Br J Pharmacol; 1998 Jun; 124(4):763-71. PubMed ID: 9690869
[TBL] [Abstract][Full Text] [Related]
19. beta(3)-adrenoceptor regulation and relaxation responses in mouse ileum.
Hutchinson DS; Evans BA; Summers RJ
Br J Pharmacol; 2000 Mar; 129(6):1251-9. PubMed ID: 10725275
[TBL] [Abstract][Full Text] [Related]
20. Ligand-directed signaling at the beta3-adrenoceptor produced by 3-(2-Ethylphenoxy)-1-[(1,S)-1,2,3,4-tetrahydronapth-1-ylamino]-2S-2-propanol oxalate (SR59230A) relative to receptor agonists.
Sato M; Horinouchi T; Hutchinson DS; Evans BA; Summers RJ
Mol Pharmacol; 2007 Nov; 72(5):1359-68. PubMed ID: 17717109
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]