Dorsal root ganglion neurons innervating skeletal muscle respond to physiological combinations of protons, ATP, and lactate mediated by ASIC, P2X, and TRPV1

被引:223
作者
Light, Alan R. [1 ,2 ]
Hughen, Ronald W. [1 ]
Zhang, Jie [3 ]
Rainier, Jon [4 ]
Liu, Zhuqing [4 ]
Lee, Jeewoo [5 ]
机构
[1] Univ Utah, Dept Anesthesiol, Salt Lake City, UT USA
[2] Univ Utah, Dept Neurobiol & Anat, Salt Lake City, UT USA
[3] Univ Utah, Dept Physiol, Salt Lake City, UT 84112 USA
[4] Univ Utah, Dept Chem, Salt Lake City, UT 84112 USA
[5] Seoul Natl Univ, Coll Pharm, Seoul, South Korea
关键词
D O I
10.1152/jn.01344.2007
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
The adequate stimuli and molecular receptors for muscle metaboreceptors and nociceptors are still under investigation. We used calcium imaging of cultured primary sensory dorsal root ganglion (DRG) neurons from C57B1/6 mice to determine candidates for metabolites that could be the adequate stimuli and receptors that could detect these stimuli. Retrograde DiI labeling determined that some of these neurons innervated skeletal muscle. We found that combinations of protons, ATP, and lactate were much more effective than individually applied compounds for activating rapid calcium increases in muscle-innervating dorsal root ganglion neurons. Antagonists for P2X, ASIC, and TRPV1 receptors suggested that these three receptors act together to detect protons, ATP, and lactate when presented together in physiologically relevant concentrations. Two populations of muscle-innervating DRG neurons were found. One responded to low metabolite levels (likely nonnoxious) and used ASIC3, P2X5, and TRPV1 as molecular receptors to detect these metabolites. The other responded to high levels of metabolites (likely noxious) and used ASIC3, P2X4, and TRPV1 as their molecular receptors. We conclude that a combination of ASIC, P2X5 and/or P2X4, and TRPV1 are the molecular receptors used to detect metabolites by muscle-innervating sensory neurons. We further conclude that the adequate stimuli for muscle metaboreceptors and lactate.
引用
收藏
页码:1184 / 1201
页数:18
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共 123 条
[1]   Effect of arterial occlusion on responses of group III and IV afferents to dynamic exercise [J].
Adreani, CM ;
Kaufman, MP .
JOURNAL OF APPLIED PHYSIOLOGY, 1998, 84 (06) :1827-1833
[2]   Responses of group III and IV muscle afferents to dynamic exercise [J].
Adreani, CM ;
Hill, JM ;
Kaufman, MP .
JOURNAL OF APPLIED PHYSIOLOGY, 1997, 82 (06) :1811-1817
[3]   Observations in man upon a blood pressure raising reflex arising from the voluntary muscles [J].
Alam, M ;
Smirk, FH .
JOURNAL OF PHYSIOLOGY-LONDON, 1937, 89 (04) :372-383
[4]   Assessment of muscle pain and hyperalgesia. Experimental and clinical findings [J].
Arendt-Nielsen, L ;
Mense, S ;
Graven-Nielsen, I .
SCHMERZ, 2003, 17 (06) :445-449
[5]   Effect of muscle acidity on muscle metabolism and fatigue during intense exercise in man [J].
Bangsbo, J ;
Madsen, K ;
Kiens, B ;
Richter, EA .
JOURNAL OF PHYSIOLOGY-LONDON, 1996, 495 (02) :587-596
[6]   LACTATE AND H+ EFFLUXES FROM HUMAN SKELETAL-MUSCLES DURING INTENSE, DYNAMIC EXERCISE [J].
BANGSBO, J ;
JOHANSEN, L ;
GRAHAM, T ;
SALTIN, B .
JOURNAL OF PHYSIOLOGY-LONDON, 1993, 462 :115-133
[7]   ATP production and efficiency of human skeletal muscle during intense exercise:: effect of previous exercise [J].
Bangsbo, J ;
Krustrup, P ;
González-Alonso, J ;
Saltin, B .
AMERICAN JOURNAL OF PHYSIOLOGY-ENDOCRINOLOGY AND METABOLISM, 2001, 280 (06) :E956-E964
[8]   Heteromultimers of DEG/ENaC subunits form H+-gated channels in mouse sensory neurons [J].
Benson, CJ ;
Xie, JH ;
Wemmie, JA ;
Price, MP ;
Henss, JM ;
Welsh, MJ ;
Snyder, PM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (04) :2338-2343
[9]   EFFECTS OF A CARRAGEENAN-INDUCED MYOSITIS ON THE DISCHARGE PROPERTIES OF GROUP-III AND GROUP-IV MUSCLE RECEPTORS IN THE CAT [J].
BERBERICH, P ;
HOHEISEL, U ;
MENSE, S .
JOURNAL OF NEUROPHYSIOLOGY, 1988, 59 (05) :1395-1409
[10]   UNMYELINATED NOCICEPTORS OF RAT PARASPINAL TISSUES [J].
BOVE, GM ;
LIGHT, AR .
JOURNAL OF NEUROPHYSIOLOGY, 1995, 73 (05) :1752-1762