Home Study Adrenergic receptors and regulation of energy expenditure - Page 1
Logged as CommonCrawl [Bot] - Logout
background image
30 Nov 2003
14:54
AR
AR204-PA44-13.tex
AR204-PA44-13.sgm
LaTeX2e(2002/01/18)
P1: GCE
10.1146/annurev.pharmtox.44.101802.121659
Annu. Rev. Pharmacol. Toxicol. 2004. 44:297­323
doi: 10.1146/annurev.pharmtox.44.101802.121659
Copyright c 2004 by Annual Reviews. All rights reserved
First published online as a Review in Advance on August 28, 2003
-A
DRENERGIC
R
ECEPTORS AND
R
EGULATION OF
E
NERGY
E
XPENDITURE
:
A Family Affair
Jacques Robidoux, Tonya L. Martin, and Sheila Collins
Departments of Pharmacology, Psychiatry, and Behavioral Sciences, and The Sarah W.
Stedman Center for Nutritional Studies, Duke University Medical Center, Durham,
North Carolina 27710; email: robid001@mc.duke.edu, tlm6@duke.edu,
colli008@mc.duke.edu
Key Words adipose tissue, uncoupling protein, signal transduction, cAMP, MAP
kinase
s Abstract The family of adrenergic receptors (ARs) expressed in adipocytes in-
cludes three sibling
ARs and two AR cousins. Together they profoundly influence
the mobilization of stored fatty acids, secretion of fat-cell derived hormones, and the
specialized process of nonshivering thermogenesis in brown adipose tissue. The two
types of fat cells that compose adipose tissue, brown and white, are structurally and
functionally distinct. Studies on the mechanisms by which individual
AR regulates
these cell-specific functions have recently uncovered new signal transduction cascades
involved in processes traditionally ascribed to adenylyl cyclase/cAMP/protein kinase
A system. They illustrate how
AR signaling can orchestrate a coordinated set of
intracellular responses for fine control of metabolic balance.
INTRODUCTION
Research over the past decade has provided an unprecedented expansion of our
knowledge about the physiology and molecular biology of the "adipose organ."
Among the newly recognized functions, adipose tissue is now appreciated to be
a bona fide endocrine organ capable of secreting a plethora of biologically active
substances with local and/or systemic actions (1­7). Prehaps the first and most
important event in this new era of adipocyte biology was the positional cloning of
the ob locus encoding a protein now called leptin (8), the long-sought lipostatic
factor postulated 50 years ago by Kennedy (9) and supported biochemically by
the elegant parabiosis experiments of Coleman (10). Expressed in adipose tissue,
leptin is a genuine adiposity signal, whose pleiotropic effects include decreasing
appetite and increasing energy expenditure through neuroendocrine action in the
central nervous system (reviewed in References 11, 12). Another exciting new
fat cell­derived factor is the adipocyte complement-related protein of 30 kDa
(Acrp30)/adipoQ/adiponectin (13­15), which appears, provisionally, to possess
insulin sensitizing activity. With these few examples there is a growing list of
0362-1642/04/0210-0297$14.00
297
Annu. Rev. Pharmacol. Toxicol. 2004.44:297-323. Downloaded from arjournals.annualreviews.org
by b-on: Universidade de Lisboa (UL) on 03/30/07. For personal use only.


guestbook
Subject :


Email :


Message :


Privacy Policy | Code of Conduct | Links