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. 2003 Dec 8;141(1):152–162. doi: 10.1038/sj.bjp.0705593

Table 1.

Effects of i.c.v. injection of different doses of GABA, GABAA/GABAB agonist/antagonists on RT and EcoG spectrum power in conscious rabbbits

Compound Dose (n) ΔRtmax (°C) ECoG power spectra
Vehicle −−−(6) +0.3±0.1  
GABA 48 μmol (6) −1.7±0.1** δ, θ
Nipecotic acid (GABA uptake inhibitor) 5 nmol (4) −0.2±0.2 NS  
  50 nmol (6) −1.4±0.2**# δ, θ
THIP (GABAA agonist) 10 nmol (4) −0.3±0.1 NS  
  30 nmol (4) −0.6±0.2**  
  60 nmol (4) −1.0±0.4**# δ
Muscimol (GABAA agonist) 18 nmol (5) −1.0±0.3**# δ, θ
R(−)baclofen (GABAB agonist) 1 nmol (4) −0.6±0.2**  
  8 nmol (6) −1.2±0.3**# ↑ δ, θ
CGP35348 (GABAB antagonist) 12 μmol (4) +0.1±0.2 NS n.e.
Bicuculline (GABAA antagonist) 1.8 nmol (4) 1.1±0.5* n.e.
CGP35348+muscimol GABAB antagonist+GABAA agonist 0.4 μmol+18 nmol (4) −0.4±0.2*  
  1.2 μmol+18 nmol (4) −0.1±0.3 NS n.e.
Bicuculline+muscimol (GABAA antagonist+GABAA agonist) 0.2 nmol+18 nmol (4) −1.2±0.3**,§  
  1.8 nmol+18 nmol (4) −1.8±0.2**, δ, θ**,↑ δ

n.e.: no effect. ↑: increase. δ: 1.1–3.3 Hz frequency band. θ: 4.6–9.2 Hz frequency band. RT data are reported as mean±s.e.m. The comparison between AUC(0–24 h) obtained after different treatments was performed using ANOVA followed by post hoc Dunnett's test.

*

P<0.05 vs vehicle;

**

P<0.001 vs vehicle;

#

NS vs 48 μmol GABA,

§

NS vs 18 nmol muscimol,

P<0.05 vs 18 nmol muscimol.