Paraventricular hypothalamic oxytocinergic cells responding to noxious stimulation and projecting to the spinal dorsal horn represent a homeostatic analgesic mechanism

2009 ◽  
Vol 30 (6) ◽  
pp. 1056-1063 ◽  
Author(s):  
Miguel Condés-Lara ◽  
Gerardo Rojas-Piloni ◽  
Guadalupe Martínez-Lorenzana ◽  
Javier Rodríguez-Jiménez
1997 ◽  
Vol 759 (1) ◽  
pp. 171-174 ◽  
Author(s):  
Horacio Vanegas ◽  
Vı́ctor Tortorici ◽  
Antonio Eblen-Zajjur ◽  
Enrique Vásquez

2007 ◽  
Vol 3 ◽  
pp. 1744-8069-3-4 ◽  
Author(s):  
Erika Polgár ◽  
Annie D Campbell ◽  
Lynsey M MacIntyre ◽  
Masahiko Watanabe ◽  
Andrew J Todd

2004 ◽  
Vol 91 (3) ◽  
pp. 1122-1133 ◽  
Author(s):  
Hong-Wei Yang ◽  
Xiao-Dong Hu ◽  
Hong-Mei Zhang ◽  
Wen-Jun Xin ◽  
Ming-Tao Li ◽  
...  

Long-term potentiation (LTP) of C-fiber-evoked field potentials in spinal dorsal horn may be relevant to hyperalgesia, an increased response to noxious stimulation. The mechanism underlying this form of synaptic plasticity is, however, still unclear. Considerable evidence has shown that calcium/calmodulin-dependent protein kinase II (CaMKII), protein kinase A (PKA), and protein kinase C (PKC) are important for LTP in hippocampus. In this study, the roles of these three protein kinases in the induction and maintenance of LTP of C-fiber-evoked field potentials were evaluated by application of specific inhibitors of CaMKII (KN-93 and AIP), PKA (Rp-CPT-cAMPS), and PKC (chelerythrine and Gö 6983) at the recording segments before and after LTP induction in urethane-anesthetized Sprague-Dawley rats. We found both KN-93 and AIP, when applied at 30 min prior to tetanic stimulation, completely blocked LTP induction. At 30 min after LTP induction, KN-93 and AIP reversed LTP completely, and at 60 min after LTP induction, they depressed spinal LTP in most rats tested. Three hours after LTP induction, however, KN-93 or AIP did not affect the spinal LTP. Rp-CPT-cAMPS, chelerythrine, and Gö 6983 blocked the spinal LTP when applied at 30 min before tetanic stimulation and reversed LTP completely at 15 min after LTP induction. In contrast, at 30 min after LTP induction, the drugs never affected the spinal LTP. These results suggest that activation of CaMKII, PKA, and PKC may be crucial for the induction and the early-phase but not for the late-phase maintenance of the spinal LTP.


Neuroreport ◽  
1994 ◽  
Vol 5 (16) ◽  
pp. 2101-2104 ◽  
Author(s):  
K. Yashpal ◽  
S. Kar ◽  
R. Quirion ◽  
C. W. Y. Hui-Chan ◽  
J. L. Henry

1995 ◽  
Vol 83 (6) ◽  
pp. 1312-1320 ◽  
Author(s):  
Hiroshi Uchida ◽  
Kazuhiro Kishikawa ◽  
J. G. Collins

Abstract Background Pentobarbital reduces low-threshold receptive field (RF) size and enhances responses of some spinal dorsal horn neurons to noxious stimulation in cats. To better understand the effects of general anesthetics on spinal sensory processing, this study was designed to determine if intravenous propofol and ketamine have similar effects.


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