Literature DB >> 34227186

Inflamed brain: Targeting immune changes and inflammation for treatment of depression.

Shinji Sakamoto1, Xiaolei Zhu1, Yuto Hasegawa1, Sadik Karma1, Mizuho Obayashi1, Emily Alway1, Atsushi Kamiya1.   

Abstract

Although there are a number of clinically effective treatments for depression, many patients exhibit treatment resistance. Recent clinical and preclinical studies reveal that peripheral and brain immune changes and inflammation are involved in the pathophysiology of depression. This 'Inflamed Brain' research provides critical clues for understanding of disease pathophysiology and many candidate molecules that are potentially useful for identifying novel drug targets for the treatment of depression. In this review, we will present clinical evidence on the role of inflammation in the pathophysiology of depression. We will also summarize current clinical trials which test drugs targeting inflammation for the treatment of patients with depression. Furthermore, we will briefly provide preclinical evidence demonstrating altered immune system function and inflammation in stress-induced animal models and will discuss the future potential of inflammation-related drug targets. Collectively, inflammatory signatures identified in clinical and preclinical studies may allow us to stratify depressive patients based on biotypes, contributing to the development of novel mechanism-based interventions that target specific patient populations.
© 2021 The Authors Psychiatry and Clinical Neurosciences © 2021 Japanese Society of Psychiatry and Neurology.

Entities:  

Keywords:  biotype; depression; drug-repositioning; inflammation; stress mouse models

Mesh:

Year:  2021        PMID: 34227186      PMCID: PMC8683253          DOI: 10.1111/pcn.13286

Source DB:  PubMed          Journal:  Psychiatry Clin Neurosci        ISSN: 1323-1316            Impact factor:   12.145


  110 in total

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3.  Metabolic profiles revealed synergistically antidepressant effects of lilies and Rhizoma Anemarrhenae in a rat model of depression.

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4.  JHU-083 selectively blocks glutaminase activity in brain CD11b+ cells and prevents depression-associated behaviors induced by chronic social defeat stress.

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Journal:  Neuropsychopharmacology       Date:  2018-08-13       Impact factor: 7.853

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6.  A randomized controlled trial of the tumor necrosis factor antagonist infliximab for treatment-resistant depression: the role of baseline inflammatory biomarkers.

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Journal:  JAMA Psychiatry       Date:  2013-01       Impact factor: 21.596

Review 7.  Ketamine and peripheral inflammation.

Authors:  Marc De Kock; Sebastien Loix; Patricia Lavand'homme
Journal:  CNS Neurosci Ther       Date:  2013-04-10       Impact factor: 5.243

8.  High heterogeneity and low reliability in the diagnosis of major depression will impair the development of new drugs.

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Journal:  BJPsych Open       Date:  2015-11-17

9.  Autonomic and Redox Imbalance Correlates With T-Lymphocyte Inflammation in a Model of Chronic Social Defeat Stress.

Authors:  Cassandra M Moshfegh; Safwan K Elkhatib; Christopher W Collins; Allison J Kohl; Adam J Case
Journal:  Front Behav Neurosci       Date:  2019-05-14       Impact factor: 3.558

10.  Modulation of the antidepressant effects of ketamine by the mTORC1 inhibitor rapamycin.

Authors:  Chadi G Abdallah; Lynnette A Averill; Ralitza Gueorguieva; Selin Goktas; Prerana Purohit; Mohini Ranganathan; Mohamed Sherif; Kyung-Heup Ahn; Deepak Cyril D'Souza; Richard Formica; Steven M Southwick; Ronald S Duman; Gerard Sanacora; John H Krystal
Journal:  Neuropsychopharmacology       Date:  2020-02-24       Impact factor: 7.853

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  1 in total

1.  Case report: Depressive disorder with peripartum onset camouflages suspected intracranial tuberculoma.

Authors:  Halwa Zakia; Shelly Iskandar
Journal:  Front Psychiatry       Date:  2022-09-29       Impact factor: 5.435

  1 in total

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