Scientific Reports (Aug 2022)

Dopamine D1-like receptor blockade and stimulation decreases operant responding for nicotine and food in male and female rats

  • Ranjithkumar Chellian,
  • Azin Behnood-Rod,
  • Ryann Wilson,
  • Karen Lin,
  • Grace Wing-Yan King,
  • Marcella Ruppert-Gomez,
  • Alexandria Nicole Teter,
  • Marcelo Febo,
  • Adriaan W. Bruijnzeel

DOI
https://doi.org/10.1038/s41598-022-18081-3
Journal volume & issue
Vol. 12, no. 1
pp. 1 – 12

Abstract

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Abstract Dopamine has been implicated in the reinforcing effects of smoking. However, there remains a need for a better understanding of the effects of dopamine D1-like receptor agonists on nicotine intake and the role of sex differences in the effects of dopaminergic drugs on behavior. This work studied the effects of D1-like receptor stimulation and blockade on operant responding for nicotine and food and locomotor activity in male and female rats. The effects of the D1-like receptor antagonist SCH 23390 (0.003, 0.01, 0.03 mg/kg) and the D1-like receptor agonist A77636 (0.1, 0.3, 1 mg/kg) on responding for nicotine and food, and locomotor activity were investigated. The effects of SCH 23390 were investigated 15 min and 24 h after treatment, and the effects of the long-acting drug A77636 were investigated 15 min, 24 h, and 48 h after treatment. Operant responding for nicotine and food and locomotor activity were decreased immediately after treatment with SCH 23390. Treatment with SCH 23390 did not have any long-term effects. Operant responding for nicotine was still decreased 48 h after treatment with A77636, and food responding was decreased up to 24 h after treatment. Treatment with A77636 only decreased locomotor activity at the 48 h time point. There were no sex differences in the effects of SCH 23390 or A77636. In conclusion, the D1-like receptor antagonist SCH 23390 reduces nicotine intake and causes sedation in rats. Stimulation of D1-like receptors with A77636 decreases nicotine intake at time points that the drug does not cause sedation.