The serotonin transporter is required for stress-evoked increases in adrenal catecholamine synthesis and angiotensin II AT(2) receptor expression

Neuroendocrinology. 2003 Oct;78(4):217-25. doi: 10.1159/000073705.

Abstract

High numbers of serotonin transporter (SERT) binding sites and high serotonin (5-HT) content are expressed in the adrenal medulla of wild-type (SERT+/+) mice. Acute restraint stress increases adrenomedullary 5-HT, norepinephrine (NE) and epinephrine (E) release, adrenomedullary tyrosine hydroxylase (TH) mRNA, and angiotensin II AT(2) receptor expression. There are no alterations in adrenal catecholamine content during restraint. In littermate SERT-/- mice, which do not express SERT binding sites, the basal adrenomedullary 5-HT content is significantly reduced and does not increase after stress. The stress-induced increase in plasma E is higher in SERT-/- than in SERT+/+ animals. In SERT-/- mice, the stress-induced increase in expression of TH mRNA does not occur, and as a consequence, adrenal E content decreases, and adrenal E and NE content are lower than that of SERT+/+ mice during restraint. In addition, instead of increased expression, stress induces a profound decrease in the number of adrenomedullary AT(2) receptors in SERT-/- mice. Our results indicate that SERT is necessary for the stress-induced increase in adrenomedullary catecholamine synthesis and AT(2) receptor expression. These data further indicate a close relationship between the adrenomedullary 5-HT and angiotensin II systems, and an important role of adrenomedullary AT(2) receptors in catecholamine synthesis and release during stress.

Publication types

  • Comparative Study

MeSH terms

  • Adrenal Glands / cytology
  • Adrenal Glands / metabolism
  • Animals
  • Binding Sites
  • Carrier Proteins / genetics
  • Carrier Proteins / metabolism*
  • Catecholamines / biosynthesis*
  • Catecholamines / blood
  • Chromatography, High Pressure Liquid
  • Cocaine / analogs & derivatives*
  • Cocaine / pharmacokinetics
  • In Situ Hybridization
  • Membrane Glycoproteins / genetics
  • Membrane Glycoproteins / metabolism*
  • Membrane Transport Proteins*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Nerve Tissue Proteins*
  • RNA, Messenger / metabolism
  • Radiopharmaceuticals / pharmacokinetics
  • Receptors, Angiotensin / genetics
  • Receptors, Angiotensin / metabolism*
  • Restraint, Physical / methods
  • Serotonin Plasma Membrane Transport Proteins
  • Stress, Physiological / metabolism*
  • Stress, Physiological / physiopathology
  • Tyrosine 3-Monooxygenase / genetics
  • Tyrosine 3-Monooxygenase / metabolism

Substances

  • Carrier Proteins
  • Catecholamines
  • Membrane Glycoproteins
  • Membrane Transport Proteins
  • Nerve Tissue Proteins
  • RNA, Messenger
  • Radiopharmaceuticals
  • Receptors, Angiotensin
  • Serotonin Plasma Membrane Transport Proteins
  • Slc6a4 protein, mouse
  • 2beta-carbomethoxy-3beta-(4-iodophenyl)tropane
  • Tyrosine 3-Monooxygenase
  • Cocaine