Literature DB >> 17471085

Selective vulnerability to ischemia in the rat spinal cord: a comparison between ventral and dorsal horn neurons.

Kazuhiro Nohda1, Terumasa Nakatsuka, Daisuke Takeda, Nobuyuki Miyazaki, Hideto Nishi, Hideki Sonobe, Munehito Yoshida.   

Abstract

STUDY
DESIGN: Whole-cell patch-clamp recordings were performed from ventral horn (VH) and dorsal horn (DH) neurons obtained from the rat spinal cord slices.
OBJECTIVE: This study investigated which is more vulnerable to ischemia, spinal VH neurons or DH neurons. SUMMARY OF BACKGROUND DATA: Spinal cord ischemia or injury sometimes causes a greater loss of motor function than of sensory function in patients. However, it is difficult to evaluate whether spinal motor neurons are more vulnerable than sensory neurons because of the anatomic complexity and a variety of physiologic factors in the spinal cord.
METHODS: Whole-cell patch-clamp recordings were performed from VH and DH neurons obtained from the spinal cord slices. Ischemia was simulated by superfusing an oxygen- and glucose-deprived medium (ischemia simulating medium [ISM]).
RESULTS: Perfusion with ISM generated an agonal depolarization in all VH and DH neurons recorded in current-clamp mode. Following ISM superfusion, an agonal inward current was produced at a holding potential of -70 mV in all VH and DH neurons tested in voltage-clamp mode. The agonal inward current consisted of a slow and subsequent rapid inward current. The average latency of the rapid inward currents after ISM exposures in VH neurons was significantly shorter than that in DH neurons. The average amplitude of the agonal inward currents in VH neurons was significantly bigger than that of DH neurons. Moreover, the recovery ratio by the reintroduction of oxygen and glucose in VH neurons was smaller than that in DH neurons.
CONCLUSIONS: These results suggest that VH neurons are more vulnerable to ischemia than DH neurons. This finding may help in achieving a better understanding of the difference between motor and sensory disturbance in spinal cord ischemia or injury patients.

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Year:  2007        PMID: 17471085     DOI: 10.1097/01.brs.0000261560.53428.90

Source DB:  PubMed          Journal:  Spine (Phila Pa 1976)        ISSN: 0362-2436            Impact factor:   3.468


  10 in total

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2.  Adenosine modulates excitatory synaptic transmission and suppresses neuronal death induced by ischaemia in rat spinal motoneurones.

Authors:  Nobuyuki Miyazaki; Terumasa Nakatsuka; Daisuke Takeda; Kazuhiro Nohda; Kazuhide Inoue; Munehito Yoshida
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Journal:  Neurocrit Care       Date:  2022-03-07       Impact factor: 3.532

10.  Exosomes Derived from Nerve Stem Cells Loaded with FTY720 Promote the Recovery after Spinal Cord Injury in Rats by PTEN/AKT Signal Pathway.

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  10 in total

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