A second tryptophan hydroxylase isoform, TPH-2 mRNA, is increased by ovarian steroids in the raphe region of macaques

Brain Res Mol Brain Res. 2005 Apr 27;135(1-2):194-203. doi: 10.1016/j.molbrainres.2004.12.011.

Abstract

Recently, a second gene that codes for the rate-limiting enzyme in serotonin synthesis was found in brain, named tryptophan hydroxylase-2 (TPH-2). We sequenced overlapping segments (251 and 510 bp) of 5' monkey TPH-2 and questioned whether TPH-2 is regulated by estrogen (E) and progesterone (P) in serotonin neurons of macaques. Monkey TPH-2 was 97% homologous to human TPH-2 and 65% homologous to monkey TPH-1 in the coding region. Spayed monkeys were administered placebo, E-only, P-only, or E + P for 1 month via Silastic implants (n = 4/treatment) and the midbrain was utilized for TPH-2 in situ hybridization (ISH). Additional monkeys (n = 3/treatment) were used to determine the relative abundance of TPH-2 mRNA with quantitative (q) RT-PCR. In the ISH assay, all of the hormone treatments caused a significant and similar increase in TPH-2 mRNA optical density (fourfold; P < 0.004) and positive pixel area (twofold; P < 0.002) over spayed controls. Treatment with E or E + P for 1 month increased the relative abundance of TPH-2 mRNA over spayed controls in the qRT-PCR assay (ANOVA P < 0.05 and P < 0.007, respectively). In conclusion, ovarian steroids stimulate TPH-2 mRNA expression, which could in turn cause an increase in serotonin synthesis. This would impact many of the neural functions that are governed by serotonin.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Analysis of Variance
  • Animals
  • DNA, Complementary / metabolism
  • Densitometry / methods
  • Estrogens / blood
  • Estrogens / pharmacology
  • Female
  • Gene Expression Regulation / drug effects*
  • Humans
  • Hysterectomy / methods
  • In Situ Hybridization / methods
  • Macaca mulatta
  • Ovariectomy / methods
  • Progesterone / blood
  • Progesterone / pharmacology
  • RNA, Messenger / metabolism
  • Raphe Nuclei / drug effects*
  • Raphe Nuclei / metabolism
  • Reverse Transcriptase Polymerase Chain Reaction / methods
  • Steroids / blood
  • Steroids / pharmacology*
  • Tryptophan Hydroxylase / chemistry
  • Tryptophan Hydroxylase / genetics
  • Tryptophan Hydroxylase / metabolism*

Substances

  • DNA, Complementary
  • Estrogens
  • RNA, Messenger
  • Steroids
  • Progesterone
  • Tryptophan Hydroxylase