4.6 Article

Faster Serotonin Clearance in CA3 Region of Hippocampus and Antidepressant-like Effect of Decynium-22 in Juvenile Mice Are Putatively Linked to Increased Plasma Membrane Monoamine Transporter Function: Implications for Efficacy of Antidepressants in Juveniles

Journal

CELLS
Volume 11, Issue 15, Pages -

Publisher

MDPI
DOI: 10.3390/cells11152454

Keywords

antidepressant; decynium-22; depression; juvenile; organic cation transporter 3; plasma membrane monoamine transporter; serotonin clearance; serotonin transporter

Categories

Funding

  1. National Institutes of Health (NIH) [1R01 MH106978]
  2. South Texas-Medical Scientist Training Program(STX-MSTP) [T32 GM113896]

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Selective serotonin reuptake inhibitors (SSRIs) are less effective in treating depression in children than in adults. This may be due to the upregulation of organic cation transporter 3 (OCT3) and plasma membrane monoamine transporter (PMAT) in juveniles, leading to faster serotonin clearance and specific blocker's antidepressant-like effects.
Selective serotonin reuptake inhibitors (SSRIs) are less efficacious in treating depression in children than in adults. SSRIs block serotonin uptake via the high-affinity, low-capacity serotonin transporter. However, the low-affinity, high-capacity organic cation transporter 3 (OCT3) and plasma membrane monoamine transporter (PMAT) are emerging as important players in serotonin uptake. We hypothesized that OCT3 and/or PMAT are functionally upregulated in juveniles, thereby buffering SSRIs' ability to enhance serotonergic neurotransmission. Unlike in adult mice, we found the OCT/PMAT blocker, decynium-22, to have standalone antidepressant-like effects in juveniles. Using in vivo high-speed chronoamperometry, we found that juveniles clear serotonin from the CA3 region of the hippocampus similar to 2-fold faster than adult mice. Cell density did not differ between ages, suggesting that faster serotonin clearance in juveniles is unrelated to faster diffusion through the extracellular matrix. Western blot and immunohistochemistry showed that juvenile mice have modestly greater expression of PMAT than adults, whereas OCT3 expression in the CA3 region of the hippocampus was similar between ages. Together, these data suggest that faster serotonin clearance and antidepressant-like effects of decynium-22 in juvenile mice may be due to functionally upregulated PMAT. Faster serotonin clearance via PMAT in juveniles may contribute to reduced therapeutic efficacy of SSRIs in children relative to adults.

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