Melanin-concentrating hormone receptor: A therapeutic target for novel anxiolytics

IF 3.3 3区 心理学 Q1 BEHAVIORAL SCIENCES
Shigeyuki Chaki
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Abstract

Anxiety disorders are chronic, disabling psychiatric disorders, and there is a growing medical need for the development of novel pharmacotherapeutic agents showing improved efficacy and an improved side effect profile as compared with the currently prescribed anxiolytic drugs. In the course of the search for next-generation anxiolytics, neuropeptide receptors have garnered interest as potential therapeutic targets, underscored by pivotal roles in modulating stress responses and findings from animal studies using pharmacological tools.

Among these neuropeptide receptors, the type 1 receptor for melanin-concentrating hormone (MCH1), which has been demonstrated to be involved in an array of physiological processes, including the regulation of stress responses and affective states, has gained attraction as a therapeutic target for drugs used in the treatment of psychiatric disorders, including anxiety disorders. To date, a plethora of MCH1 antagonists have been synthesized, and studies using MCH1 antagonists and genetically manipulated mice lacking MCH1 have revealed that the blockade of MCH1 produces anxiolytic-like effects across diverse rodent paradigms. In addition, MCH1 antagonists have been demonstrated to show a rapid onset of antidepressant-like effects; therefore, they may be effective for conditions commonly encountered in patients with anxiety disorders, which is an advantage for anxiolytic drugs. Notably, MCH1 antagonists have not manifested the undesirable side effects observed with the currently prescribed anxiolytics. All these preclinical findings testify to the potential of MCH1 antagonists as novel anxiolytics.

Although there are still issues that need to be resolved prior to the initiation of clinical trials, such as elucidating the precise neuronal mechanisms underlying their anxiolytic effects and exploring pertinent biomarkers that can be used in clinical trials, MCH1 blockade appears to be an attractive way to tackle anxiety disorders.

黑色素浓缩激素受体:新型抗焦虑药的治疗靶点
焦虑症是一种慢性、致残性精神疾病,与目前处方中的抗焦虑药物相比,开发疗效更好、副作用更小的新型药物治疗药物的医疗需求日益增长。在寻找下一代抗焦虑药物的过程中,神经肽受体作为潜在的治疗靶点引起了人们的兴趣,其在调节应激反应中的关键作用以及使用药理学工具进行动物实验的结果都凸显了这一点。在这些神经肽受体中,黑色素浓缩激素(MCH1)的 1 型受体已被证明参与了一系列生理过程,包括应激反应和情感状态的调节。迄今为止,已经合成了大量的 MCH1 拮抗剂,利用 MCH1 拮抗剂和缺乏 MCH1 的遗传操作小鼠进行的研究表明,在不同的啮齿类动物范例中,阻断 MCH1 可产生类似抗焦虑的效果。此外,MCH1 拮抗剂已被证明具有快速起效的抗抑郁样作用;因此,它们可能对焦虑症患者常遇到的情况有效,这是抗焦虑药物的一个优势。值得注意的是,MCH1 拮抗剂并没有表现出目前处方抗焦虑药的不良副作用。所有这些临床前研究结果都证明了 MCH1 拮抗剂作为新型抗焦虑药物的潜力。尽管在启动临床试验之前仍有一些问题需要解决,例如阐明其抗焦虑作用的神经元精确机制,以及探索可用于临床试验的相关生物标志物,但阻断 MCH1 似乎是解决焦虑症的一种有吸引力的方法。
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来源期刊
CiteScore
6.40
自引率
2.80%
发文量
122
审稿时长
38 days
期刊介绍: Pharmacology Biochemistry & Behavior publishes original reports in the areas of pharmacology and biochemistry in which the primary emphasis and theoretical context are behavioral. Contributions may involve clinical, preclinical, or basic research. Purely biochemical or toxicology studies will not be published. Papers describing the behavioral effects of novel drugs in models of psychiatric, neurological and cognitive disorders, and central pain must include a positive control unless the paper is on a disease where such a drug is not available yet. Papers focusing on physiological processes (e.g., peripheral pain mechanisms, body temperature regulation, seizure activity) are not accepted as we would like to retain the focus of Pharmacology Biochemistry & Behavior on behavior and its interaction with the biochemistry and neurochemistry of the central nervous system. Papers describing the effects of plant materials are generally not considered, unless the active ingredients are studied, the extraction method is well described, the doses tested are known, and clear and definite experimental evidence on the mechanism of action of the active ingredients is provided.
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