Regional CNS densities of monoamine receptors in alcohol-naive alcohol-preferring P and -nonpreferring NP rats

Alcohol. 1997 Mar-Apr;14(2):141-8. doi: 10.1016/s0741-8329(96)00117-6.

Abstract

The densities of subtypes of serotonin (5-HT) and dopamine (DA) receptors were determined in the CNS of alcohol-naive alcohol-preferring P and -nonpreferring NP lines of rats. Autoradiography studies were undertaken to measure the densities of 5-HT1B sites labelled with 100 pM [125I](-)-iodocyanopindolol, 5-HT3 sites labelled with 2 nM [3H]LY 278584, and D1 sites labelled with 1 nM[3H]SCH 23390. Membrane binding, using tissue combined from the olfactory bulb, olfactory tubercle, and nucleus accumbens, was carried out to determine Kd and B max values for the binding of 0.25-8.0 nM[3H]7-OH DPAT to D3 sites. Among the 48 regions measured for differences in 5-HT1B recognition sites, statistically significant differences (p < 0.05) were found only in the cingulate and retrosplenial cortices, in the lateral and medial septum, and in the lateral nucleus of the amygdala, with lower values being found in the P than the NP line. There were no significant differences in the regional CNS densities of D1 or 5-HT3 sites between the P and NP lines. There were also no differences between the rat lines in the Kd or Bmax values for [3H]7-OH DPAT binding to D3 sites. The lower densities of 5-HT1B sites in the CNS of the P compared to the NP rats may be a result of reduced numbers of 5-HT1B presynaptic autoreceptors as well as postsynaptic receptors in the P line. The observation that there are no differences in the amount of radioligand binding to D1, 5-HT3, and D3 sites between the P and NP lines suggests that the disparate alcohol drinking behaviors of these two lines is not associated with an innate alteration in the densities of these receptor subtypes.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Autoradiography
  • Benzazepines / metabolism
  • Brain / metabolism*
  • Cell Membrane / metabolism
  • Dopamine Agonists / metabolism
  • Ethanol / administration & dosage*
  • Indazoles / metabolism
  • Iodocyanopindolol
  • Male
  • Nucleus Accumbens / metabolism
  • Olfactory Bulb / metabolism
  • Olfactory Pathways / metabolism
  • Pindolol / analogs & derivatives
  • Pindolol / metabolism
  • Rats
  • Receptors, Biogenic Amine / metabolism*
  • Receptors, Dopamine D1 / metabolism
  • Receptors, Dopamine D2 / metabolism
  • Receptors, Dopamine D3
  • Receptors, Serotonin / metabolism
  • Serotonin Antagonists / metabolism
  • Tetrahydronaphthalenes / metabolism
  • Tropanes / metabolism

Substances

  • Benzazepines
  • Dopamine Agonists
  • Drd3 protein, rat
  • Indazoles
  • Receptors, Biogenic Amine
  • Receptors, Dopamine D1
  • Receptors, Dopamine D2
  • Receptors, Dopamine D3
  • Receptors, Serotonin
  • Serotonin Antagonists
  • Tetrahydronaphthalenes
  • Tropanes
  • LY 278584
  • Ethanol
  • Iodocyanopindolol
  • Pindolol
  • 7-hydroxy-2-N,N-dipropylaminotetralin