共 124 条
The functions of TRPA1 and TRPV1: moving away from sensory nerves
被引:355
作者:
Fernandes, E. S.
[2
]
Fernandes, M. A.
[1
]
Keeble, J. E.
[1
]
机构:
[1] Kings Coll London, Inst Pharmaceut Sci, Sch Biomed Sci, London SE1 9NH, England
[2] Kings Coll London, Sch Med, Cardiovasc Div, London SE1 9NH, England
基金:
英国生物技术与生命科学研究理事会;
关键词:
TRPV1;
TRPA1;
capsaicin;
non-neuronal;
expression;
functionality;
RECEPTOR POTENTIAL CHANNELS;
VANILLOID-RELATED CHANNELS;
GENE-RELATED PEPTIDE;
SMOOTH-MUSCLE-CELLS;
RAT URINARY-BLADDER;
CAPSAICIN RECEPTOR;
ION-CHANNEL;
NEUROGENIC INFLAMMATION;
IN-VIVO;
TRANSIENT-RECEPTOR-POTENTIAL-VANILLOID-1;
TRPV1;
D O I:
10.1111/j.1476-5381.2012.01851.x
中图分类号:
R9 [药学];
学科分类号:
100702 [药剂学];
摘要:
The transient receptor potential vanilloid 1 and ankyrin 1 (TRPV1 and TRPA1, respectively) channels are members of the TRP superfamily of structurally related, non-selective cation channels. It is rapidly becoming clear that the functions of TRPV1 and TRPA1 interlink with each other to a considerable extent. This is especially clear in relation to pain and neurogenic inflammation where TRPV1 is coexpressed on the vast majority of TRPA1-expressing sensory nerves and both integrate a variety of noxious stimuli. The more recent discovery that both TRPV1 and TRPA1 are expressed on a multitude of non-neuronal sites has led to a plethora of research into possible functions of these receptors. Non-neuronal cells on which TRPV1 and TRPA1 are expressed vary from vascular smooth muscle to keratinocytes and endothelium. This review will discuss the expression, functionality and roles of these non-neuronal TRP channels away from sensory nerves to demonstrate the diverse nature of TRPV1 and TRPA1 in addition to a direct role in pain and neurogenic inflammation.
引用
收藏
页码:510 / 521
页数:12
相关论文

