“…Abbreviations: 3 V, third ventricle; AQ, cerebral aqueduct; CMT, central medial nucleus of thalamus; DR, dorsal raphe nucleus; fx, fornix; LD, laterodorsal nucleus of thalamus; LDT, laterodorsal tegmental nucleus; LGN, lateral geniculate nucleus of thalamus; LP, lateral posterior nucleus of thalamus; MD, mediodorsal nucleus of thalamus; ml, medial lemniscus; MR, median raphe nucleus; PAG, periaqueductal gray; PH, posterior hypothalamus; PSV, principal sensory nucleus of trigeminal nerve; PV, paraventricular nucleus of thalamus; RE, nucleus reuniens of thalamus; RF, reticular formation; RM, raphe magnus, RPC, reticularis pontis caudalis; RT, reticular nucleus of thalamus; V, motor nucleus of trigeminal nerve; VB, ventrobasal complex of thalamus; VM, ventromedial nucleus of thalamus; VTN, ventral tegmental nucleus; ZI, zona incerta anesthesia, Muindi et al (2016) described enhanced levels of c-fos expression in PB during the (passive) emergence from isoflurane anesthesia, and further reported that PB stimulation produced arousal and return of the righting reflex during continuous isoflurane administration. Consistent with this, Luo et al (2018) demonstrated that PB activity was suppressed during propofol or isoflurane anesthesia and strongly enhanced with emergence from anesthesia. Further, chemogenetic PB activation significantly shortened the recovery time from these GAs (Luo et al, 2018).…”