| Project/Area Number |
09671572
|
|---|
| Research Category |
Grant-in-Aid for Scientific Research (C)
|
| Allocation Type | Single-year Grants |
|---|
| Section | 一般 |
|---|
| Research Field |
Anesthesiology/Resuscitation studies
|
|---|
| Research Institution | Saga Medical School |
|---|
Principal Investigator |
TOTOKI Tadahide Saga Medical School, Professor, 医学部, 教授 (20038722)
|
|---|
| Co-Investigator(Kenkyū-buntansha) |
MORIMOTO Masatosi Saga Medical School, Assistant Professor, 医学部, 助教授 (90136482)
HAMADA Tomoko Saga Medical School, Assistant, 医学部, 助手 (30284657)
HARANO Kiyoshi Saga Medical School, Assistant Professor, 医学部, 助教授 (30038848)
|
|---|
| Project Period (FY) |
1997 – 1999
|
| Project Status |
Completed (Fiscal Year 1999)
|
| Budget Amount *help |
¥2,900,000 (Direct Cost: ¥2,900,000)
Fiscal Year 1999: ¥1,600,000 (Direct Cost: ¥1,600,000)
Fiscal Year 1998: ¥600,000 (Direct Cost: ¥600,000)
Fiscal Year 1997: ¥700,000 (Direct Cost: ¥700,000)
|
|---|
| Keywords | phantom pain / neuropathic pain / allodynia / neurotransmitters / neuropeptides / deafferentation pain / rats / immunohistochemistry |
|---|
| Research Abstract |
We attempted to develop an experimental animal model for peripheral neuropathic pain including the phantom pain. Under anesthesia, median, ulnar and raidiar nerves of one side of the rat (SD and hairless) were cut (group 1) or pull out (group 2). Sensitivity of the fore paw to mechanical stimulation was tested with von Frey hair for the next 5 months in two groups. The general behavior of each rat was noted during the entire test period.
Following arm denervation, autotomy in 50% (group 1) and 20% (group 2) exploded. In the hairless rat, the ulcer of the skin was observed in 50% (both group). The test with mechanical stimulation in all groups did not produce a mechanical allodynia. Seven days following axotomy of the nerves, some large and medium sized cells in the dorsal root ganglia (C4〜Th1) displayed neuropeptide Y (NPY)-like immunoreactivity (IR), and marked increases in the numbers were observed for the next 5 months. The number of NPY-IR cells in the stellate ganglion (SG) increased in the group 2. A few strong staining cells for the nicotinamaide adenin dinucleotide phosphate ? Diaphorase (NADPH-d) were observed in the SG of the group 1 for the next 7 days. NADPH-d staining cells were not detected in the normal rat SG.
We concluded that the study of the neuropathic pain including the phantom pain must be done using different species and families.
|
