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用于惊恐障碍的新型研究性治疗药物。

Novel investigational therapeutics for panic disorder.

机构信息

Hermanas Hospitalarias - Villa San Benedetto Menni Hospital, Department of Clinical Neurosciences, FoRiPsi , via Roma 16, 22032, Albese con Cassano, Como , Italy +39031 4291511 ; +39031 427246 ;

出版信息

Expert Opin Investig Drugs. 2015 Apr;24(4):491-505. doi: 10.1517/13543784.2014.996286. Epub 2014 Dec 24.

Abstract

INTRODUCTION

Panic disorder (PD) is a common disabling anxiety disorder associated with relevant social costs. Effective anti-panic medications exist but have several drawbacks. From a clinical perspective, there is still a strong unmet need for more effective, faster acting and more tolerable therapeutic treatments.

AREAS COVERED

The authors review the available results on novel mechanism-based anti-panic drugs that are under investigation in animal studies up to Phase II studies. The preclinical studies investigated include: the modulators of the glutamate/orexin/cannabinoid systems, corticotrophin-releasing factor 1 (CRF1)/arginine vasopressine V₁B/angiotensin II receptor antagonists and neuropeptide S. The Phase I/II studies investigated include: the modulators of the glutamate system, isoxazoline derivative, translocator protein (18 kDa) ligands and CRF1/neurokinin receptor antagonists.

EXPERT OPINION

There has been little progress in recent times. However, glutamate- and orexin-related molecular targets may represent very promising opportunities for treating panic attacks. Very preliminary findings suggest that the antagonists of CRF1 and A-II receptors may have anti-panic properties. However, new medications for PD are far from being implemented in clinical use. The reasons are multiple, including: the heterogeneity of the disorder, the translational validity of animal models and the insufficient use of biomarkers in preclinical/clinical studies. Nevertheless, biomarker-based strategies, pharmacogenomics, 'personalized psychiatry' and the NIH's Research Domain Criteria approach could help to remove those obstacles limiting drug development.

摘要

简介

惊恐障碍(PD)是一种常见的致残性焦虑障碍,与相关的社会成本有关。有效的抗惊恐药物确实存在,但也存在一些缺点。从临床角度来看,仍然迫切需要更有效、作用更快和更耐受的治疗方法。

涵盖领域

作者回顾了在动物研究中至 II 期研究中正在研究的新型基于机制的抗惊恐药物的现有结果。研究中涉及的临床前研究包括:谷氨酸/食欲素/大麻素系统调节剂、促肾上腺皮质激素释放因子 1(CRF1)/精氨酸加压素 V₁B/血管紧张素 II 受体拮抗剂和神经肽 S。研究中涉及的 I/II 期研究包括:谷氨酸系统调节剂、异恶唑啉衍生物、转位蛋白(18 kDa)配体和 CRF1/神经激肽受体拮抗剂。

专家意见

最近进展甚微。然而,谷氨酸和食欲素相关的分子靶点可能是治疗惊恐发作的非常有前途的机会。非常初步的发现表明,CRF1 和 A-II 受体拮抗剂可能具有抗惊恐特性。然而,治疗惊恐障碍的新药远未在临床应用中得到实施。原因有很多,包括:该疾病的异质性、动物模型的转化有效性以及临床前/临床研究中生物标志物的使用不足。尽管如此,基于生物标志物的策略、药物基因组学、“个性化精神病学”和 NIH 的研究领域标准方法可能有助于消除那些限制药物开发的障碍。

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