Enhanced endocannabinoid tone as a potential target of pharmacotherapy

被引:88
作者
Toczek, Marek [1 ]
Malinowska, Barbara [1 ]
机构
[1] Med Univ Bialystok, Dept Expt Physiol & Pathophysiol, Mickiewicz Str 2A, PL-15222 Bialystok, Poland
关键词
Endocannabinoids; Endocannabinoid system; Anadamide; 2-Arachidonoylglycerol; FAAH inhibitors; MAGL inhibitors; COX inhibitors; TRPV1; antagonists; ACID AMIDE HYDROLASE; TRANSPORT INHIBITOR AM404; MONOACYLGLYCEROL LIPASE INHIBITION; IMPROVES FUNCTIONAL RECOVERY; CB1 CANNABINOID RECEPTORS; DUAL FAAH/MAGL INHIBITORS; SELECTIVE FAAH INHIBITOR; N-ARACHIDONOYL-SEROTONIN; ENDOGENOUS CANNABINOIDS; RAT MODEL;
D O I
10.1016/j.lfs.2018.04.054
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
1001 ;
摘要
The endocannabinoid system is up-regulated in numerous pathophysiological states such as inflammatory, neurodegenerative, gastrointestinal, metabolic and cardiovascular diseases, pain, and cancer. It has been suggested that this phenomenon primarily serves an autoprotective role in inhibiting disease progression and/or diminishing signs and symptoms. Accordingly, enhancement of endogenous endocannabinoid tone by inhibition of endocannabinoid degradation represents a promising therapeutic approach for the treatment of many diseases. Importantly, this allows for the avoidance of unwanted psychotropic side effects that accompany exo-genously administered cannabinoids. The effects of endocannabinoid metabolic pathway modulation are complex, as endocannabinoids can exert their actions directly or via numerous metabolites. The two main strategies for blocking endocannabinoid degradation are inhibition of endocannabinoid-degrading enzymes and inhibition of endocannabinoid cellular uptake. To date, the most investigated compounds are inhibitors of fatty acid amide hydrolase (FAAH), an enzyme that degrades the endocannabinoid anandamide. However, application of FAAH inhibitors (and consequently other endocannabinoid degradation inhibitors) in medicine became questionable due to a lack of therapeutic efficacy in clinical trials and serious adverse effects evoked by one specific compound. In this paper, we discuss multiple pathways of endocannabinoid metabolism, changes in endocannabinoid levels across numerous human diseases and corresponding experimental models, pharmacological strategies for enhancing endocannabinoid tone and potential therapeutic applications including multi-target drugs with additional targets outside of the endocannabinoid system (cyclooxygenase-2, cholinesterase, TRPV1, and PGF(2 alpha)-EA receptors), and currently used medicines or medicinal herbs that additionally enhance endocannabinoid levels. Ultimately, further clinical and preclinical studies are warranted to develop medicines for enhancing endocannabinoid tone.
引用
收藏
页码:20 / 45
页数:26
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