ACHE and movement disorder: In zebrafish, the effects of BTP were studied during embryo–larval development, with an emphasis on toxicity (mortality and lethal effects), ED effects (HPG-, HPI-, and HPT-axis), and neurobehavioral disorders (movement disorders and AChE activity), whereas the studies in larvae were restricted only to pancreatic beta cells; in adults, BTP was evaluated as a neurobehavioral disruptor.