Investigational drugs for pruritus

被引:14
作者
Benecke, Heike [1 ]
Lotts, Tobias [2 ,3 ]
Staender, Sonja [2 ,3 ]
机构
[1] Univ Med Gottingen, Ctr Nanoscale Microscopy & Mol Physiol Brain, D-37073 Gottingen, Germany
[2] Univ Hosp Munster, Competence Ctr Chron Pruritus, D-48149 Munster, Germany
[3] Univ Hosp Munster, Dept Dermatol, D-48149 Munster, Germany
关键词
chronic pruritus; neurokinin-1; receptor; opioid receptors; therapy of CP; HISTAMINE H-4 RECEPTOR; NERVE GROWTH-FACTOR; ITCH-ASSOCIATED RESPONSE; GASTRIN-RELEASING-PEPTIDE; FUNCTIONAL VANILLOID RECEPTORS; INHIBITS SCRATCHING BEHAVIOR; MAST-CELL DEGRANULATION; GENE-RELATED PEPTIDE; ATOPIC-DERMATITIS; SUBSTANCE-P;
D O I
10.1517/13543784.2013.813932
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Introduction: Chronic pruritus (CP), defined as itch lasting for > 6 weeks, is a burdensome symptom of several different diseases, dermatological and systemic, with a high negative impact on the quality of life of patients. Given the manifold aetiologies of CP, therapy is often difficult. In recent years, however, novel substances have been developed for treatment of certain CP entities and identified targets. Areas covered: In this review, the authors present a survey of targets currently believed to be promising (H4R, IL-31, MOR, KOR, GRPR, NGF, NK-1R, TRP channels) and related investigational drugs that are in the preclinical or clinical stage of development. Some substances have already undergone clinical testing, but only one of them (nalfurafine) has been licensed so far. Many of them are most likely to exert their effects on the skin and interfere there with the cutaneous neurobiology of CP. Expert opinion: Currently, the most promising candidates for new therapeutic agents in CP are neurokinin-1 receptor antagonists and substances targeting the kappa-or mu-opioid receptor, or both. They have the potential to target the neuronal pathway of CP and are thus of interest for several CP entities. The goal for the coming years is to validate these concepts and move forward in developing new drugs for the therapy of CP.
引用
收藏
页码:1167 / 1179
页数:13
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