scholarly journals Pinch-current injection defines two discharge profiles in mouse superficial dorsal horn neurones,in vitro

2007 ◽  
Vol 578 (3) ◽  
pp. 787-798 ◽  
Author(s):  
B. A. Graham ◽  
A. M. Brichta ◽  
R. J. Callister
Keyword(s):  
Dorsal Horn ◽  
Current Injection ◽  
Superficial Dorsal Horn ◽  
Pinch Current ◽  
Dorsal Horn Neurones

Recording Temperature Affects the Excitability of Mouse Superficial Dorsal Horn Neurons, In Vitro

2008 ◽  
Vol 99 (5) ◽  
pp. 2048-2059 ◽  
Author(s):  
B. A. Graham ◽  
A. M. Brichta ◽  
R. J. Callister
Keyword(s):  
Spinal Cord ◽  
Elevated Temperature ◽  
Dorsal Horn ◽  
Current Injection ◽  
Resting Membrane Potential ◽  
Temperature Sensitive ◽  
Superficial Dorsal Horn ◽  
Pain Mechanisms

Superficial dorsal horn (SDH) neurons in laminae I–II of the spinal cord play an important role in processing noxious stimuli. These neurons represent a heterogeneous population and are divided into various categories according to their action potential (AP) discharge during depolarizing current injection. We recently developed an in vivo mouse preparation to examine functional aspects of nociceptive processing and AP discharge in SDH neurons and to extend investigation of pain mechanisms to the genetic level of analysis. Not surprisingly, some in vivo data obtained at body temperature (37°C) differed from those generated at room temperature (22°C) in spinal cord slices. In the current study we examine how temperature influences SDH neuron properties by making recordings at 22 and 32°C in transverse spinal cord slices prepared from L3–L5 segments of adult mice (C57Bl/6). Patch-clamp recordings (KCH3SO4 internal) were made from visualized SDH neurons. At elevated temperature all SDH neurons had reduced input resistance and smaller, briefer APs. Resting membrane potential and AP afterhyperpolarization amplitude were temperature sensitive only in subsets of the SDH population. Notably, elevated temperature increased the prevalence of neurons that did not discharge APs during current injection. These reluctant firing neurons expressed a rapid A-type potassium current, which is enhanced at higher temperatures and thus restrains AP discharge. When compared with previously published whole cell recordings obtained in vivo (37°C) our results suggest that, on balance, in vitro data collected at elevated temperature more closely resemble data collected under in vivo conditions.

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