Since the first cases of neuromyelitis optica (NMO) had been described by Eugene Devic in 1894, the understanding of pathogenesis and clinical presentations of the disease broadened considerably (Wingerchuk et al., 2015). The discovery of an association of NMO with the presence of serum antibodies against aquaporin 4 (AQP4) facilitated the diagnostic process of the disease and allowed for better differentiation between NMO and multiple sclerosis (MS) variants. In the central nervous system (CNS), the water channel AQP4, involved in the processes of osmoregulation, is highly expressed on astrocytic end-feet (forming part of the blood-brain barrier)