Allopregnanolone is required for prepulse inhibition deficits induced by D1 dopamine receptor activation

Psychoneuroendocrinology. 2019 Oct:108:53-61. doi: 10.1016/j.psyneuen.2019.06.009. Epub 2019 Jun 14.

Abstract

Introduction: The extraction of salient information from the environment is modulated by the activation of dopamine receptors. Using rodent models, we previously reported that gating deficits caused by dopamine receptor activation - as measured by the prepulse inhibition (PPI) of startle - are effectively opposed by inhibitors of the steroidogenic enzyme 5α-reductase (5αR). The specific 5αR isoenzyme and steroids implicated in these effects, however, remain unknown.

Methods: The effects of the selective D1 dopamine receptor agonist SKF-82958 (SKF, 0.3 mg/kg, IP) and D2 receptor agonist quinpirole (QUIN, 0.5 mg/kg, IP) were tested in the startle reflex and PPI of knockout (KO) mice for either 5αR type 1 (5αR1) or type 2 (5αR2). Furthermore, we established whether these effects may be modified by the 5α-reduced steroids dihydroprogesterone (DHP), allopregnanolone (AP), dihydrotestosterone (DHT), 5α-androstane-3α,17β-diol (3α-diol), or androsterone. To test the mechanisms whereby 5αR products may alter the PPI-disrupting properties of D1 agonists, we studied the involvement of GABA-A and PXR, two receptors targeted by neuroactive steroids. Specifically, we tested the effects of SKF in combination with the GABA-A antagonist bicuculline, as well as in KO mice for the GABA-A δ subunit and PXR.

Results: 5αR1, but not 5αR2, knockout (KO) mice were insensitive to the PPI-disrupting effects of SKF. This sensitivity was reinstated by AP (3 mg/kg, IP), but not other 5α-reduced steroids. The PPI deficits induced by SKF were not modified by bicuculline, δ-subunit KO mice and PXR KO mice.

Conclusions: These results collectively suggest that 5αR1 enables the negative effects of D1 dopamine receptor activation on information processing via production of AP. The contribution of AP to the PPI-disrupting mechanisms of D1 receptor agonists, however, do not appear to be mediated by either GABA-A or PXR receptors.

Keywords: 5α-reductase; Allopregnanolone; Behavioral studies; D(1)receptors; Dopamine; Sensorimotor gating.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • 3-Oxo-5-alpha-Steroid 4-Dehydrogenase / metabolism*
  • 3-Oxo-5-alpha-Steroid 4-Dehydrogenase / physiology
  • Animals
  • Benzazepines / pharmacology
  • Dopamine / metabolism
  • Dopamine / pharmacology
  • Male
  • Mice
  • Mice, Knockout
  • Pregnanolone / pharmacology*
  • Prepulse Inhibition / drug effects
  • Quinpirole / pharmacology
  • Receptors, Dopamine / metabolism
  • Receptors, Dopamine D1 / drug effects
  • Receptors, Dopamine D1 / metabolism*
  • Receptors, Dopamine D2 / drug effects
  • Receptors, Dopamine D2 / metabolism
  • Reflex, Startle / drug effects
  • Sensory Gating / physiology

Substances

  • Benzazepines
  • Receptors, Dopamine
  • Receptors, Dopamine D1
  • Receptors, Dopamine D2
  • Quinpirole
  • SK&F 82958
  • Pregnanolone
  • 3-Oxo-5-alpha-Steroid 4-Dehydrogenase
  • Dopamine