Exposure to loud noises not only leads to trauma and loss of output from the ear, but also alters downstream central auditory circuits. A perceptual consequence of noise-induced central auditory disruption is impairment in gap-induced prepulse inhibition, also known as gap detection. Recent studies have implicated cortical parvalbumin-positive (PV) inhibitory interneurons in gap detection and prepulse inhibition. Here we show that exposure to loud noises specifically reduces the density of cortical PV but not somatostatin-positive (SOM) interneurons in the primary auditory cortex (AI) in mice (C57BL/6) of both sexes. Optogenetic activation of PV neurons produced less cortical inhibition in noise-exposed than sham-exposed animals, indicative of reduced PV neuron function. Activation of SOM neurons resulted in similar levels of cortical inhibition in noise- and sham-exposed groups. Furthermore, chemogenetic activation of PV neurons with the hM3-based DREADD (designer receptor exclusively activated by designe...