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Mechanism of neural circuit reorganization in the brain that produces ectopic pain 脑内神经回路重组产生异位痛的机制
Pub Date : 2022-07-15 DOI: 10.11154/pain.37.97
M. Miyata
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引用次数: 0
Neurorehabilitation for pain 神经康复治疗疼痛
Pub Date : 2022-07-15 DOI: 10.11154/pain.37.75
M. Osumi, M. Sumitani
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引用次数: 0
Effects of acetaminophen on neuronal activity in the mouse locus coeruleus 对乙酰氨基酚对小鼠蓝斑区神经元活动的影响
Pub Date : 2022-03-30 DOI: 10.11154/pain.37.16
Iwao Seki, Ayumi Nakamura, Keisuke Koga, Hiroyuki Aono, H. Furue
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引用次数: 0
Chronic pain and opioids —how to control proper prescribing ? 慢性疼痛和阿片类药物——如何控制正确的处方?
Pub Date : 2022-03-30 DOI: 10.11154/pain.37.1
E. Kalso, M. Iseki
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引用次数: 0
Effect of Pulse Irradiation with a 10–W Semiconductor Laser on pressure pain threshold and temporal summation 10W半导体激光器脉冲辐照对压痛阈值和时间总和的影响
Pub Date : 2022-03-30 DOI: 10.11154/pain.37.26
Nobuyuki Takeuchi, M. Matsumoto
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引用次数: 0
Pharmacotherapy: Exploring an individualized therapy for neuropathic pain 药物治疗:探索神经性疼痛的个体化治疗
Pub Date : 2021-09-30 DOI: 10.11154/pain.36.173
Munetaka Hirose
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引用次数: 0
Brain imaging study for central sensitization 中枢致敏的脑成像研究
Pub Date : 2021-09-30 DOI: 10.11154/pain.36.180
K. Wakaizumi
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引用次数: 0
Analgesic mechanism of Goshajinkigan for neuropathic pain Goshajinkigan治疗神经性疼痛的镇痛机制
Pub Date : 2021-09-30 DOI: 10.11154/pain.36.154
Miho Nakanishi, S. Fukui, H. Kitagawa
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引用次数: 0
Expression of TrkA and GFRα1, and their coexpression in muscle innervating primary afferent neurons in rats TrkA和GFRα1在大鼠肌肉神经原代传入神经元中的表达及其共表达
Pub Date : 2021-09-30 DOI: 10.11154/pain.36.147
K. Mizumura, Kimiko Kobayashi, S. Murase
On the way of analyzing the mechanism of delayed onset muscle soreness, author’s group found that nerve growth factor (NGF) and glial cell line derived neurotrophic factor (GDNF) synergistically interact to induce muscular mechanical hyperalgesia. However, it is believed that NGF and GDNF work on different sets of DRG neurons that express NGF receptor, TrkA or GDNF receptor, GFR α 1–RET. However, this result was obtained from skin–innervating neurons or whole DRG neurons. It is not known whether muscle innervating DRGs are similar. In this experiment we examined whether it is also true for muscle innervating DRG neurons. We identified muscle innervating DRG neurons using retrograde tracing with Fluoro–Gold. Under anesthesia FG (4%, 10 μl) was injected to 10 points each of medial and lateral head of gastrocnemius muscle (GC). Ten to eleven days later rats were perfused and fixed under deep anesthesia. Using serial sections immunohistochemistry for FG and double in situ hybridization for TrkA and GFR α 1 were performed. As a result 39%–50% of FG+ DRG neurons were TrkA+, and 69–77% were GFR α 1+. Co–expression of TrkA and GFR α 1 was observed in 24%–29% DRG neurons innervating GC. The size distribution of FG + DRG neurons did not show a skewness in small size range (< 600 μm 2 ), rather distributed equally in small to large cell ranges. Size distribution of TrkA+ neurons and double positive (TrkA+ and GFR α 1+) also showed no skewness in small size range and distributed widely from small to large size. A part of these TrkA+ ⁄ GFR α 1+ coexpressing neurons might be the site of synergistic interaction of NGF and GDNF.
在分析迟发性肌肉酸痛机制的过程中,笔者课题组发现神经生长因子(NGF)和神经胶质细胞系衍生神经营养因子(GDNF)协同作用可诱导肌肉机械性痛觉过敏。然而,人们认为NGF和GDNF作用于表达NGF受体TrkA或GDNF受体GFR α 1-RET的不同组的DRG神经元。然而,这一结果是在皮肤神经支配神经元或整个DRG神经元中获得的。目前尚不清楚肌肉支配drg是否相似。在本实验中,我们检验了支配DRG神经元的肌肉是否也是如此。我们用氟金逆行示踪方法鉴定了支配DRG神经元的肌肉。麻醉下将FG (4%, 10 μl)注射于腓肠肌内、外侧头各10个点。10 ~ 11天后,大鼠灌注并在深度麻醉下固定。采用连续切片免疫组化法检测FG,双原位杂交法检测TrkA和GFR α 1。结果FG+ DRG神经元中TrkA+占39% ~ 50%,GFR α 1+占69 ~ 77%。TrkA和GFR α 1在支配GC的24% ~ 29%的DRG神经元中共表达。FG + DRG神经元的大小分布在小尺寸范围(< 600 μm 2)内不呈现偏态,在大小细胞范围内均匀分布。TrkA+和双阳性(TrkA+和GFR α 1+)神经元的大小分布在小尺寸范围内无偏态,由小到大分布广泛。这些TrkA+ / GFR α 1+共表达神经元的一部分可能是NGF和GDNF协同作用的部位。
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引用次数: 0
Involvement of TRP channels in analgesic action of Kampo medicine TRP通道参与汉布药的镇痛作用
Pub Date : 2021-09-30 DOI: 10.11154/pain.36.163
Yi Dai
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引用次数: 0
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Pain Research
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