非人类灵长类动物疼痛模型的脑激活功能磁共振成像

Pain Research Pub Date : 2020-03-31 DOI:10.11154/pain.35.45
Hiroki Ushirozako, G. Yoshida, T. Hasegawa, Yu Yamato, Takahiro Natsume, S. Ogawa, Y. Awaga, A. Hama, H. Takamatsu, Y. Matsuyama
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引用次数: 0

摘要

功能性磁共振成像(fMRI)有望成为疼痛的生物标志物,因为它可以客观地评估与神经元对抗疼痛活动相关的脑血流量变化。我们开发了食蟹猕猴的疼痛模型,因为它在大脑区域的结构和功能方面与人类更兼容,而大脑区域被认为与人类的疼痛有关。除了人类,食蟹猴是分布最广的灵长类动物,从日本到北非都有。由于猕猴是可用于侵入性实验的动物中最接近人类的物种,因此它们被广泛用于了解人类大脑的机制。本研究的目的是使用功能磁共振成像来阐明猕猴模型中与疼痛相关的大脑激活区域。通常,动物模型中的疼痛测试是基于对疼痛刺激的回避行为。然而,我们在丙泊酚麻醉下使用fMRI作为一种更客观的评估方法,确定了疼痛相关的大脑激活区域。在木瓜蛋白酶诱导的椎间盘源性腰痛的猕猴模型中,岛叶皮层的活动是对腰部压迫刺激的反应。在奥沙利铂诱导的神经性冷超敏反应的猕猴模型中,岛叶皮层的激活也发生在对冷刺激的反应中。作为评估普瑞巴林、度洛西汀和曲马多的结果者は増加の一途にあり,中でも腰痛に苦しむ患 者の数は非常に多く,さらに様々な原因によっ て生じるため,痛みによって賦活化される脳領 与吗啡、美洛昔康和对乙酰氨基酚相比,只有吗啡表现出行为有效性,并抑制了子宫内膜异位症腹痛引起的丘脑激活。有人认为,大脑激活区域可能会因各种可能导致疼痛的条件而改变,因为急性疼痛增加了岛叶皮层的激活,慢性疼痛增加了丘脑的激活。这项研究证明了fMRI作为疼痛生物标志物的有用性,使用猕猴的fMRI分析可能为将研究结果转化为人类患者提供优势。因此,这些研究将有助于开发针对每种疼痛的新型止痛药,并有助于大脑研究领域的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Brain activation in non–human primate pain model using functional MRI
Functional magnetic resonance imaging (fMRI) is expected as a biomarker of pain because it can objectively evaluate changes in cerebral blood flow associated with neuron activity against pain. We have developed pain models for cynomolgus macaques because it is more compatible with humans in regard to the structures and functions of brain regions which is suggested to be involved in pain in humans. Aside from humans, the cynomolgus macaques are the most widespread primate genus, ranging from Japan to North Africa. Since the macaques are the animal species closest to humans among those which can be used for invasive experiments, they are widely used to understand the mechanisms of the human brain. The purpose of this study is to elucidate pain–related brain activation regions in the macaque models using fMRI. Generally, pain testing in animal models has been based on avoidance behavior against pain stimuli. However, we identified pain– related brain activation regions using fMRI under propofol anesthesia as a more objective evaluation method. In the macaque model of chymopapain–induced discogenic low back pain, the activity of the insular cortex occurred in response to lumbar compression stimulation. In the macaque model of oxaliplatin–induced neuropathic cold hypersensitivity, activation of the insular cortex also occurred in response to cold stimuli. As a result of evaluating pregabalin, duloxetine and tramadol, only 者は増加の一途にあり,中でも腰痛に苦しむ患 者の数は非常に多く,さらに様々な原因によっ て生じるため,痛みによって賦活化される脳領 ing morphine, meloxicam and acetaminophen, only morphine showed behavioral effectiveness and suppressed activation of thalamus due to abdominal pain from endometriosis. It was suggested that the brain activation regions could change due to various conditions that can cause the pain, as the acute pain increased activation in the insula cortex and the chronic pain increased activation in the thalamus. This study demonstrated the usefulness of fMRI as a pain biomarker, and fMRI analysis using the macaques might provide an advantage for the translation of the findings to human patients. Therefore, these study will contribute to the development of new analgesics for each pain as well as to the progress in the areas of brain research.
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Pain Research
Pain Research CLINICAL NEUROLOGY-
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