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

Rachel L. Sanchez, Arubala P. Reddy, Maria L. Centeno, Jessica A. Henderson, Cynthia L. Bethea

    Research output: Contribution to journalArticlepeer-review

    81 Scopus citations

    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.

    Original languageEnglish (US)
    Pages (from-to)194-203
    Number of pages10
    JournalMolecular Brain Research
    Volume135
    Issue number1-2
    DOIs
    StatePublished - Apr 27 2005

    Keywords

    • Estrogen
    • In situ hybridization
    • Macaques
    • Progesterone
    • Quantitative PCR
    • Serotonin
    • Tryptophan hydroxylase genes

    ASJC Scopus subject areas

    • Molecular Biology
    • Cellular and Molecular Neuroscience

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