THIP is a hypnotic drug, which displays a unique pharmacological profile, since it activates a subset of extrasynaptic GABA_A receptors containing -subunits. It is important to study the physiology and pharmacology of these extrasynaptic receptors, and to determine how THIP interacts with other hypnotics and anaesthetics. Here, we study the modulation of the extrasynaptic response to THIP using three classes of GABA_A receptor ligands. In whole-cell recordings from mouse neocortical layer 2/3 pyramidal cells, THIP induced an extrasynaptic tonic current of 44 ± 5 pA. The benzodiazepine site agonist and hypnotic zolpidem (500 nM), which displays selectivity for _1/2/3- and ₂-containing receptors, did not alter the tonic current induced by THIP. The anaesthetic etomidate (1 µM), which shows selectivity for ₂- and ₃-containing GABA_A receptors, potentiated the THIP current by 126%. Etomidate also induced a small tonic GABA_A current per se. The anesthetic propofol (1 µM), which displays broad-spectrum modulatory effects on several GABA_A receptor subtypes, enhanced the tonic THIP current by 117 %. Finally, all three compounds modulated the function of intrasynaptic receptors activated by synaptically released GABA. Our study shows that the extrasynaptic GABA_A receptors responsible for the tonic THIP conductance likely do not contain ₁-, ₂-, ₃-, and ₂-subunits. Thus, the tonic GABAergic conductance in the neocortex is presumably mediated by _42/3 receptors, which are likely to play a major role for neocortical excitability. Furthermore, our study has deepened the knowledge about the cellular actions of THIP, as well as THIP’s interactions with other hypnotics and anaesthetics.