Afflicting over 50 million people worldwide and demonstrating growing global trends of abuse, amphetamine-type stimulant abuse poses a significant public health burden. No effective pharmacological treatments exist for amphetamine-type stimulant use disorders, underscoring a critical need to identify novel, effective therapeutic targets. Amphetamine exerts its actions in part by targeting high-affinity, low-capacity monoamine transporters, particularly the dopamine transporter (DAT). However, th
It’s not all DAT: harnessing the potential of organic cation transporter 3 inhibition to selectively attenuate amphetamine reinforcement and dopamine release
Lauren E. Honan·Lynette C. Daws·W. Anthony Owens·Sangbin Shin·Yeon Ha Ju·Yonggong Shi·Rebecca E. Horton·Lief E. Fenno·Gregory T. Collins·Briana Mason
