Literature DB >> 24345533

Norepinephrine transporter occupancy by nortriptyline in patients with depression: a positron emission tomography study with (S,S)-[¹⁸F]FMeNER-D₂.

Harumasa Takano1, Ryosuke Arakawa1, Tsuyoshi Nogami1, Masayuki Suzuki1, Tomohisa Nagashima1, Hironobu Fujiwara1, Yasuyuki Kimura1, Fumitoshi Kodaka1, Keisuke Takahata1, Hitoshi Shimada1, Yoshitaka Murakami2, Amane Tateno3, Makiko Yamada1, Hiroshi Ito4, Kazunori Kawamura5, Ming-Rong Zhang5, Hidehiko Takahashi1, Motoichiro Kato6, Yoshiro Okubo3, Tetsuya Suhara1.   

Abstract

Norepinephrine transporter (NET) plays important roles in the treatment of various neuropsychiatric disorders, such as depression and attention deficit hyperactivity disorder (ADHD). Nortriptyline is a NET-selective tricyclic antidepressant (TCAs) that has been widely used for the treatment of depression. Previous positron emission tomography (PET) studies have reported over 80% serotonin transporter occupancy with clinical doses of selective serotonin reuptake inhibitors (SSRIs), but there has been no report of NET occupancy in patients treated with relatively NET-selective antidepressants. In the present study, we used PET and (S,S)-[18¹⁸F]FMeNER-D₂ to investigate NET occupancies in the thalamus in 10 patients with major depressive disorder taking various doses of nortriptyline, who were considered to be responders to the treatment. Reference data for the calculation of occupancy were derived from age-matched healthy controls. The result showed approximately 50-70% NET occupancies in the brain as a result of the administration of 75-200 mg/d of nortriptyline. The estimated effective dose (ED₅₀) and concentration (EC₅₀) required to induce 50% occupancy was 65.9 mg/d and 79.8 ng/ml, respectively. Furthermore, as the minimum therapeutic level of plasma nortriptyline for the treatment of depression has been reported to be 70 ng/ml, our data indicate that this plasma nortriptyline concentration corresponds to approximately 50% NET occupancy measured with PET, suggesting that more than 50% of central NET occupancy would be appropriate for the nortriptyline treatment of patients with depression.

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Year:  2013        PMID: 24345533     DOI: 10.1017/S1461145713001521

Source DB:  PubMed          Journal:  Int J Neuropsychopharmacol        ISSN: 1461-1457            Impact factor:   5.176


  10 in total

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Authors:  Arnold F Jacobson; Mark I Travin
Journal:  J Nucl Cardiol       Date:  2015-05-15       Impact factor: 5.952

2.  Imaging the pathophysiology of major depressive disorder - from localist models to circuit-based analysis.

Authors:  Michael T Treadway; Diego A Pizzagalli
Journal:  Biol Mood Anxiety Disord       Date:  2014-03-07

3.  Preclinical to clinical translation of CNS transporter occupancy of TD-9855, a novel norepinephrine and serotonin reuptake inhibitor.

Authors:  Jacqueline A M Smith; D L Bourdet; D L Patil; O T Daniels; Y-S Ding; J-D Gallezot; S Henry; K H S Kim; S Kshirsagar; W J Martin; G P Obedencio; E Stangeland; P R Tsuruda; W Williams; R E Carson; S T Patil
Journal:  Int J Neuropsychopharmacol       Date:  2014-12-13       Impact factor: 5.176

4.  Neuroprotective Effect of Nortriptyline in Overt Hepatic Encephalopathy Through Attenuation of Mitochondrial Dysfunction.

Authors:  Ji Heun Jeong; Do Kyung Kim; Nam-Seob Lee; Young-Gil Jeong; Ho Won Kim; Jong-Seok Kim; Seung-Yun Han
Journal:  ASN Neuro       Date:  2018 Jan-Dec       Impact factor: 4.146

5.  Reduction of depression-like behavior in rat model induced by ShRNA targeting norepinephrine transporter in locus coeruleus.

Authors:  Xiangdong Du; Ming Yin; Lian Yuan; Guangya Zhang; Yan Fan; Zhe Li; Nian Yuan; Xiaoli Lv; Xueli Zhao; Siyun Zou; Wei Deng; Thomas R Kosten; Xiang Yang Zhang
Journal:  Transl Psychiatry       Date:  2020-05-04       Impact factor: 6.222

6.  Occupancy of Norepinephrine Transporter by Duloxetine in Human Brains Measured by Positron Emission Tomography with (S,S)-[18F]FMeNER-D2.

Authors:  Sho Moriguchi; Harumasa Takano; Yasuyuki Kimura; Tomohisa Nagashima; Keisuke Takahata; Manabu Kubota; Soichiro Kitamura; Tatsuya Ishii; Masanori Ichise; Ming-Rong Zhang; Hitoshi Shimada; Masaru Mimura; Jeffrey H Meyer; Makoto Higuchi; Tetsuya Suhara
Journal:  Int J Neuropsychopharmacol       Date:  2017-12-01       Impact factor: 5.176

7.  A Positron Emission Tomography Study of Norepinephrine Transporter Occupancy and Its Correlation with Symptom Response in Depressed Patients Treated with Quetiapine XR.

Authors:  Lakshmi N Yatham; Vesna Sossi; Yu-Shin Ding; Nasim Vafai; Shyam Sundar Arumugham; Taj Dhanoa; Raymond W Lam; David J Bond; Joseph H Puyat
Journal:  Int J Neuropsychopharmacol       Date:  2018-02-01       Impact factor: 5.176

8.  Serotonin and Norepinephrine Transporter Occupancy of Tramadol in Nonhuman Primate Using Positron Emission Tomography.

Authors:  Ryosuke Arakawa; Akihiro Takano; Christer Halldin
Journal:  Int J Neuropsychopharmacol       Date:  2019-01-01       Impact factor: 5.176

9.  Venlafaxine ER Blocks the Norepinephrine Transporter in the Brain of Patients with Major Depressive Disorder: a PET Study Using [18F]FMeNER-D2.

Authors:  Ryosuke Arakawa; Per Stenkrona; Akihiro Takano; Jonas Svensson; Max Andersson; Sangram Nag; Yuko Asami; Yoko Hirano; Christer Halldin; Johan Lundberg
Journal:  Int J Neuropsychopharmacol       Date:  2019-04-01       Impact factor: 5.176

10.  Differential Potency of Venlafaxine, Paroxetine, and Atomoxetine to Inhibit Serotonin and Norepinephrine Reuptake in Patients With Major Depressive Disorder.

Authors:  Fahad Aldosary; Sandhaya Norris; Philippe Tremblay; Jonathan S James; James C Ritchie; Pierre Blier
Journal:  Int J Neuropsychopharmacol       Date:  2022-04-19       Impact factor: 5.176

  10 in total

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