"These results underscore the importance of determining whether, as in the C. elegans nervous system, a diversity of biogenic amine-gated chloride channels function in the human brain," said H. Robert Horvitz of the McGovern Institute for Brain Research at MIT and senior author of the study. "If so, such channels might define novel therapeutic targets for neuropsychiatric disorders, such as depression and schizophrenia."
In 2000, Horvitz's group discovered that serotonin activates a chloride channel they called MOD-1, which inhibits neuronal activity in C. elegans.