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. Author manuscript; available in PMC: 2015 Sep 1.
Published in final edited form as: Anesth Analg. 2014 Sep;119(3):558–569. doi: 10.1213/ANE.0000000000000321

Figure 3.

Figure 3

Anesthetic effects on paired pulse population spike responses recorded from CA1 neurons were concentration-dependent and exhibited differential involvement of GABAA receptor-mediated inhibition. Low concentrations of pentobarbital (50 μM; A) produced little effect on first pulse responses, but reduced second pulse responses to approximately 20% of control. This depression of second pulse responses appeared to be mediated entirely by enhanced GABAA-mediated inhibition, because it was completely reversed by bicuculline. Higher concentrations of pentobarbital (200 μM; B and 300 μM; C) produced increasing degrees of first pulse response depression that was only partially reversed by bicuculline. Similarly, second pulse depression produced by these concentrations was only partially reversed by the GABAA receptor antagonist. A transient excitatory effect on first pulse responses became evident at the highest concentrations of pentobarbital studied (300 and 500 μM; C and D). Symbols represent the mean ± SD for at least five time matched experiments from separate brain slices for each concentration studied.