Neurotensin and Neurotensin Receptors in Stress-related Disorders:Pathophysiology & Novel Drug Targets

神经降压素 焦虑 神经肽 受体 神经科学 心理学 萧条(经济学) 上瘾 医学 精神科 内科学 经济 宏观经济学
作者
Grigorios Kyriatzis,Michel Khrestchatisky,Lotfi Ferhat,Εkaterini Chatzaki
出处
期刊:Current Neuropharmacology [Bentham Science Publishers]
卷期号:22 (5): 916-934 被引量:26
标识
DOI:10.2174/1570159x21666230803101629
摘要

Abstract: Neurotensin (NT) is a 13-amino acid neuropeptide widely distributed in the CNS that has been involved in the pathophysiology of many neural and psychiatric disorders. There are three known neurotensin receptors (NTSRs), which mediate multiple actions, and form the neurotensinergic system in conjunction with NT. NTSR1 is the main mediator of NT, displaying effects in both the CNS and the periphery, while NTSR2 is mainly expressed in the brain and NTSR3 has a broader expression pattern. In this review, we bring together up-to-date studies showing an involvement of the neurotensinergic system in different aspects of the stress response and the main stress-related disorders, such as depression and anxiety, post-traumatic stress disorder (PTSD) and its associated symptoms, such as fear memory and maternal separation, ethanol addiction, and substance abuse. Emphasis is put on gene, mRNA, and protein alterations of NT and NTSRs, as well as behavioral and pharmacological studies, leading to evidence-based suggestions on the implicated regulating mechanisms as well as their therapeutic exploitation. Stress responses and anxiety involve mainly NTSR1, but also NTSR2 and NTSR3. NTSR1 and NTSR3 are primarily implicated in depression, while NTSR2 and secondarily NTSR1 in PTSD. NTSR1 is interrelated with substance and drug abuse and NTSR2 with fear memory, while all NTSRs seem to be implicated in ethanol consumption. Some of the actions of NT and NTSRs in these pathological settings may be driven through interactions between NT and corticotrophin releasing factor (CRF) in their regulatory contribution, as well as by NT’s pro-inflammatory mediating actions.
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