TABLE 5.
Drug Pharmacologya | Doses | Route | Strain/Species | Sex | ICSS Procedureb | Drug Effectc | Dependent Measure | Reference | ||
---|---|---|---|---|---|---|---|---|---|---|
Drug Name | Mechanism | Structure | Parameter | |||||||
mg/kg | ||||||||||
Nicotine | nAChR agonist | 0.025–0.8 | s.c. | Long Evans rat | Male | Hybrid | Frequency | Mixed | ↓θ0 | Bauco and Wise, 1994 |
Nicotine | nAChR agonist | 0.06–1.0 | s.c. | F-344 rat | Male | Discrete trial | Amplitude | Facilitation | ↓CIT | Huston-Lyons and Kornetsky, 1992 |
Pentobarbital | GABAA + allosteric modulator | 2.5–10 | i.p. | Long Evans rat | Male | Hybrid | Frequency | Facilitation | ↓M50 | Bossert and Franklin, 2003 |
Diazepam | GABAA + allosteric modulator | 0.5–4.0 | i.p. | C57Bl6/J mouse | Male | Hybrid | Frequency | Facilitation | ↓θ0 | Straub et al., 2010 |
Toluene. | GABAA + allosteric modulator/NMDA ant | 480–5000 ppm | C57Bl6/J mouse | Male | Hybrid | Frequency | Mixed | ↓M50 ↑↓rate | Tracy et al., 2014 | |
Phencyclidine | NMDA antagonist | 0.5–5.0 | i.p. | CDF rat | Male | Discrete trial | Amplitude | Facilitation | ↓CIT | Kornetsky et al., 1979 |
Phencyclidine | NMDA antagonist | 0.3–5.6 | i.p. | Wistar rat | Male | Discrete trial | Amplitude | No effect | Bespalov et al., 1999 | |
Phencyclidine | NMDA antagonist | 2.5 and 5.0 | i.p. | Long Evans rat | Male | Hybrid | Frequency | Mixed | ↓θ0 ↑↓rate | Carlezon and Wise, 1993b |
MK801 | NMDA antagonist | 0.01–0.3 | i.p. | Lister rat | Male | Free operant | Mixed | ↑↓rate | Herberg and Rose, 1989 | |
MK801 | NMDA antagonist | 0.032–0.32 | i.p. | Sprague-Dawley rat | Male | Hybrid | Frequency | Mixed | ↑↓rate | Hillhouse et al., 2014 |
Ketamine | NMDA antagonist | 0.3–100 | i.p. | Lister rat | Male | Free operant | Mixed | ↑↓rate | Herberg and Rose, 1989 | |
Ketamine | NMDA antagonist | 3.2–10 | i.p. | Sprague-Dawley rat | Male | Hybrid | Frequency | Depression | ↓rate | Hillhouse et al., 2014 |
THC | CB1/CB2 agonist | 1.0 | i.p. | Fischer 344 rat | Male | Hybrid | Frequency | No effect | Lepore et al., 1996 | |
THC | CB1/CB2 agonist | 1.0 | i.p. | Lewis rat | Male | Hybrid | Frequency | Facilitation | ↓θ0 ↓M50 | Lepore et al., 1996 |
THC | CB1/CB2 agonist | 1.0 | i.p. | Sprague-Dawley rat | Male | Hybrid | Frequency | Facilitation | ↓θ0 | Lepore et al., 1996 |
THC | CB1/CB2 agonist | 0.1 and 1.0 | i.p. | Sprague-Dawley rat | Male | Hybrid | Frequency | Mixed | ↑↓EF36.7 | Katsidoni et al., 2013 |
THC | CB1/CB2 agonist | 1.0–10 | i.p. | Sprague-Dawley rat | Male | Hybrid | Frequency | Depression | ↓rate | Kwilasz and Negus, 2012 |
Caffeine | adenosine antagonist | 1.0–20 | i.p. | Wistar rat | Male | Discrete trial | Amplitude | Mixed | ↑↓CIT | Bespalov et al., 1999 |
Testosterone | anabolic steroid | 50 μg | Sherman rat | Male | Free operant | Facilitation | ↑rate | Caggiula and Hoebel, 1966 | ||
Tripelennamine | H1 antagonist | 0.625–20 | i.p. | CDF rat | Male | Discrete trial | Amplitude | Facilitation | ↓CIT | Unterwald et al., 1984 |
Rate, response rate; CIT, current-intensity threshold; θ0, theta-0 threshold; M50 or EF50, frequency maintaining 50% maximum rate; EF36.7, frequency maintaining 36.7% maximum rate.
Mechanism of action or drug class.
First column indicates structure of experimental session (see text for details). Second column indicates stimulation parameter under manipulation across trials.
Most prominent drug effect on ICSS.