视频暴力与攻击行为的神经成像研究进展

认知神经科学促进了心理学领域有关视频暴力与攻击行为的神经生理机制研究.近几年,国外研究者使用功能性磁共振成像研究了视频暴力与攻击行为的神经生理机制,并提出了新的攻击行为模型:神经发展模型.研究发现:长时间暴露在视频暴力下人类对暴力的威胁的脑反应是真实的并且可以察觉到的;能导致前额皮层、杏仁核、前扣带皮层、海马和海马回的激活;能增加潜在的攻击行为.文章介绍了认知神经科学领域中视频暴力和攻击行为神经成像研究的发展现状并展望了其前景.     

人脑对不同频率穴位电刺激反应的功能性磁共振成像

利用功能性磁共振方法研究人脑对不同频率穴位体表电刺激（transcutaneous electric nerve stimulation,TENS)的反应。实验对11名志愿得进行了22次脑部功能性磁共振成像。成像过程中,每名志愿者分别接受了2和100HzTENS刺激,刺激部位为左腿足三里和三阴交穴,结果为不同频率TENS都激活了初级和次级躯体感觉区,频率特异性的激活信号出现在与运动相关的区域、丘脑、边缘系统和联络皮层。结果显示,在相同穴位给予不同频率的TENS要以在大脑引起不同的反应,提示2和100HzTENS可能激活了不同的神经通路,这些神经通路分别在中枢神经系统起着不同的作用。     

应用基于内源信号的光学成像技术的视觉脑研究现状

基于脑内源信号的光学成像技术是近来国际上出现的一种脑功能成像方法。该技术既无毒,又具有较高的空间分辨率,因而被迅速应用于动物的视觉、听觉、体感皮层功能构筑的研究中。本文综述了这种光学脑功能成像在视觉脑研究方面所取得的重要进展,并分析了该方法与其他脑成像技术、微电极单细胞技术的关系。报道了国内自行研制第、套脑功能光学成像系统的研究工作,该系统已在猫初级视觉皮层不同深度获得了清晰的方位功能图,并已经和     

AMPA受体介导的神经元和星形胶质细胞网络编程小鼠胡须感觉适应

动物感觉输入的适应性影响了它们对外界环境改变的意识和反应.感觉通路各层次,诸如感受器、传入神经和中枢系统等,反应活性的降低可能与感觉适应性相关联.在感觉适应过程中,皮层局部网络中神经元和星形胶质细胞对信号的编程机制仍有待进一步研究.利用活体双光子成像、电生理记录即药理学方法,我们分析了小鼠barrel皮层神经元和星形胶质应答重复的胡须感觉输入动力学.相同特征的胡须感觉刺激诱发了神经元和星形胶质细胞反应活性的降低,并且它们的活动在空间上和时间上去同步化,神经元和星形胶质细胞之间的缺少协调性.这种神经元和星形胶质细胞功能在空间和时间性质上的下调被局部施加AMPA受体脱敏感抑制剂所逆转.因此,在胡须感觉适应过程中,barrel皮层神经元和星形胶质细胞反应活性的下降和去同步化是由AMPA受体脱敏感参与介导完成的.     

痛觉预期的神经生理研究进展

疼痛是一种复杂的感觉和情绪体验,除了伤害性刺激本身的理化性质外,不同的心理和认知状态对痛感受也有很大的影响。其中一个可以显著调节疼痛的心理因素就是预期。本文将对近年来有关痛觉预期的神经生物学机制研究进展做一简要综述。     

综述与专论：运动诱发的镇痛效应：脊髓、皮层下和皮层机制

在健康受试者或部分慢性疼痛人群中，一定强度和时长的运动锻炼或针对性的运动疗法，已被广泛验证可以有效提高疼痛阈值并改善疼痛症状。上述运动诱发的镇痛效应（exercise induced hypoalgesia,EIH）被认为与痛觉内源性调控系统在神经系统不同水平上的调控作用紧密联系；合适类型的运动刺激可以在脊髓水平诱发镇痛效应，亦可激活脊髓以上高位中枢神经系统的痛觉内源性调控系统，进而对脊髓水平的伤害性反应进行调控。病理性痛状态下，EIH的产生与运动皮层的激活水平以及痛觉下行抑制作用均有关。研究脊髓、皮层下和皮层水平EIH效应的确切机制，将为非药物运动手段预防疼痛慢性化提供帮助。     

哺乳动物大脑感觉皮层对多种感觉信息整合的研究进展

脑对多感觉信息的整合是人和高等动物获取环境中有意义信息的重要方式。长期以来科学界一直认为,脑对不同感觉刺激(包括视觉、听觉、躯体感觉等)信息的分析和加工由不同的感觉皮层介导,最终在联络皮层进行整合,形成综合性的感觉和意识,但最近的一些实验证据显示,以前被认为只负责对单一感觉刺激分析和处理的感觉皮层亦可受其他感觉刺激的影响并直接参与多感觉信息的整合作用,这些新的发现对过去传统的大脑皮层功能分区概念提出了严峻的挑战。就近些年来有关感觉皮层(主要包括听觉、视觉和躯体感觉皮层)对多感觉刺激信息整合的研究进行综述,以增加人们对大脑皮层功能的新认识,为感觉信息处理和编码及感觉信息整合的后续研究提供借鉴。     

多方式认知功能成像研究进展

对大脑结构和功能的深入研究要求认知功能成像技术同时具有高时间分辨率和高空间分辨率.多方式认知功能成像通过不同成像技术fMRI/PET和EEG/MEG的结合,能够同时在空间定位和时间过程上研究大脑认知活动的动态过程.多方式认知功能成像已经被成功地应用于选择性注意、视觉通路、随意运动和语义加工等的研究,并揭示了相关大脑活动的空间和时间特征.今后的研究将进一步提高多方式认知功能成像的时空分辨率和准确性,以更深入地探索认知功能的神经机制.     

fMRI与DTI在神经科学研究中的联合应用

功能磁共振成像(fMRI)和扩散张量成像(DTI)是近年来磁共振成像领域出现的两种新的成像技术,它们各具特色。功能磁共振成像能对人脑相关任务激活区进行准确的功能定位并提供相关皮层区域的磁共振信号改变特征信息,但时于脑白质相关改变则不能提供任何信息;扩散张量成像则是目前能够在体呈现人脑解剖连接的唯一手段,采用它能对人脑组织,包括灰质和白质的扩散特性进行定量研究,并且能够形象显示人脑生理或病理状态下的纤维束形态、走行等,但扩散张量成像不能提供皮层功能情况信息。功能磁共振成像和扩散张量成像技术具有很强的互补性,二者联合在神经科学研究中具有广阔的应用前景。目前也正成为神经科学研究领域的热点之一。本文从功能磁共振成像和扩散张量成像的原理、特点,二者结合应用的具体方法以及目前二者在神经科学各基础及临床学科结合应用的研究进展进行了综述。     

脑功能成像用于疼痛相关情绪的研究进展

本文综述了近年来脑功能成像技术应用于疼痛情绪研究的进展,介绍了不同的皮层亚区和皮层下结构在疼痛相关情绪的产生和调控中的作用.指明了扣带回、前额叶皮质、岛叶、海马结构和杏仁核在疼痛相关情绪产生以调控过程中所起的作用.     

Pathobiology of visceral pain: molecular mechanisms and therapeutic implications V. Central nervous system processing of somatic and visceral sensory signals

Somatic and visceral sensation, including pain perception, can be studied noninvasively in humans with functional brain imaging techniques. Positron emission tomography and functional magnetic resonance imaging have identified a series of cerebral regions involved in the processing of somatic pain, including the anterior cingulate, insular, prefrontal, inferior parietal, primary and secondary somatosensory, and primary motor and premotor cortices, the thalamus, hypothalamus, brain stem, and cerebellum. Experimental evidence supports possible specific roles for individual structures in processing the various dimensions of pain, such as encoding of affect in the anterior cingulate cortex. Visceral sensation has been examined in the setting of myocardial ischemia, distension of hollow viscera, and esophageal acidification. Although knowledge regarding somatic sensation is more extensive than the information available for visceral sensation, important similarities have emerged between cerebral representations of somatic and visceral pain.     

Expertise modulates the perception of pain in others

Perceiving the pain of others activates a large part of the pain matrix in the observer [1]. Because this shared neural representation can lead to empathy or personal distress [2, 3], regulatory mechanisms must operate in people who inflict painful procedures in their practice with patient populations in order to prevent their distress from impairing their ability to be of assistance. In this functional magnetic resonance imaging MRI study, physicians who practice acupuncture were compared to naive participants while observing animated visual stimuli depicting needles being inserted into different body parts, including the mouth region, hands, and feet. Results indicate that the anterior insula somatosensory cortex, periaqueducal gray, and anterior cingulate cortex were significantly activated in the control group, but not in the expert group, who instead showed activation of the medial and superior prefrontal cortices and the temporoparietal junction, involved in emotion regulation and theory of mind.     

Influence of surgical pain stress on the blood-brain barrier permeability in rats

Effect of surgical pain stress on the blood-brain barrier permeability was investigated in rats. The animals were divided into four groups: Group 1: control, Group 2: immobilization stress, Group 3: acute hypertension, Group 4: immobilization stress + surgical pain stress.Bilateral hid paw surgical wounds for cannulations were applied in animals' inguinal regions under diethyl-ether anesthesia, then the animals were awaken from anesthesia to produce surgical pain stress. Evans-blue was used as a blood-brain barrier tracer. There is no significantly blood-brain barrier breakdown after short-time immobilization stress, but after adrenalin hypertension blood-brain barrier permeability was increased especially on frontal and occipital cortices in 50% of the animals. Surgical pain stress increased blood-brain barrier permeabiliy in comparison to acute adrenalin-induced hypertension (p < 0.01). In surgical pain stress-induced animals distinct Evans-blue leakage was observed in the occipital, frontal and parieto-temporal cortices.     

Frontal Lobe Hemodynamic Responses to Painful Stimulation: A Potential Brain Marker of Nociception

The purpose of this study was to use functional near-infrared spectroscopy (fNIRS) to examine patterns of both activation and deactivation that occur in the frontal lobe in response to noxious stimuli. The frontal lobe was selected because it has been shown to be activated by noxious stimuli in functional magnetic resonance imaging studies. The brain region is located behind the forehead which is devoid of hair, providing a relative ease of placement for fNIRS probes on this area of the head. Based on functional magnetic resonance imaging studies showing blood-oxygenation-level dependent changes in the frontal lobes, we evaluated functional near-infrared spectroscopy measures in response to two levels of electrical pain in awake, healthy human subjects (n = 10; male = 10). Each subject underwent two recording sessions separated by a 30-minute resting period. Data collected from 7 subjects were analyzed, containing a total of 38/36 low/high intensity pain stimuli for the first recording session and 27/31 pain stimuli for the second session. Our results show that there is a robust and significant deactivation in sections of the frontal cortices. Further development and definition of the specificity and sensitivity of the approach may provide an objective measure of nociceptive activity in the brain that can be easily applied in the surgical setting.     

Functional brain mapping of pain perception

In this review, we summarize the contribution of functional imaging to the question of nociception in humans. In the beginning of the 90's, brain areas supposed to be involved in physiological pain processes were almost exclusively the primary somatosensory area (SI), thalamus, and anterior cingulate cortex. In spite of these a priori hypotheses, the first imaging studies revealed that the main brain areas and those providing the most consistent activations in pain conditions were the insular and the SII cortices, bilaterally. This has been confirmed with other techniques such as intracerebral recordings of evoked potentials after nociceptive stimulations with laser showing a consistent response in the operculo-insular area which amplitude correlates with pain intensity. In spite of electrode implantations in other areas of the brain, only rare and inconsistent responses have been found outside the operculo-insular cortices. With electrical stimulation delivered directly in the brain, it has also been shown that stimulation in this area only--and not in other brain areas--was able to elicit a painful sensation. Thus, over the last 15 years, the operculo-insular cortex has been re-discovered as a main area of pain integration, mainly in its sensory and intensity aspects. In neuropathic pain also, these areas have been demonstrated as being abnormally recruited, bilaterally, in response to innocuous stimuli. These results suggest that plastic changes may occur in brain areas that were pre-defined for generating pain sensations. Conversely, when the brain activations concomitant to pain relief is taken into account, a large number of studies pointed out medial prefrontal and rostral cingulate areas as being associated with pain controls. Interestingly, these activations may correlate with the magnitude of pain relief, with the activation of the PAG, and, at least in some instances, with the involvement of endogenous opioids.     

Postnatal changes in functional activities of the pig's brain: a combined functional magnetic resonance imaging and immunohistochemical study

Developmental changes in brain activation after pain stimulation and after passive movement of the hind paw were assessed by functional magnetic resonance imaging (fMRI) in pigs of postnatal ages 2, 4 and 6 months. Response patterns were correlated with histological maturation parameters. At 2 months, fMRI failed to detect brain activation after pain stimulation and revealed weak, but widespread activation after passive movement. At 4 months, strong reaction of numerous cortical areas on the contralateral side was seen after pain stimulation. Following passive movement, activation was weaker but more widespread, and the brainstem was also involved. By 6 months, cortical activation became more restricted to the contralateral sensory cortex and brainstem after pain stimulation and to the contralateral sensory and ipsilateral premotor and motor cortices after passive movement. Neocortical synaptophysin immunoreaction increased significantly between 2 and 4 months and slightly decreased by 6 months. The density of GABA-immunoreactive neurons and fibers significantly increased, reaching a maximum at 6 months. Our studies indicate that remodeling of synapses and development of inhibitory GABA neurons last until 6 months postnatally, when the fMRI response of the pig's brain also attains its mature adult pattern.     

Functional neuroanatomy of the hypnotic state

The neural mechanisms underlying hypnosis and especially the modulation of pain perception by hypnosis remain obscure. Using PET we first described the distribution of regional cerebral blood flow during the hypnotic state. Hypnosis relied on revivification of pleasant autobiographical memories and was compared to imaging autobiographical material in "normal alertness". The hypnotic state was related to the activation of a widespread set of cortical areas involving occipital, parietal, precentral, premotor, and ventrolateral prefrontal and anterior cingulate cortices. This pattern of activation shares some similarities with mental imagery, from which it mainly differs by the relative deactivation of precuneus. Second, we looked at the anti-nociceptive effects of hypnosis. Compared to the resting state, hypnosis reduced pain perception by approximately 50%. The hypnosis-induced reduction of affective and sensory responses to noxious thermal stimulation were modulated by the activity in the midcingulate cortex (area 24a'). Finally, we assessed changes in cerebral functional connectivity related to hypnosis. Compared to normal alertness (i.e., rest and mental imagery), the hypnotic state, significantly enhanced the functional modulation between midcingulate cortex and a large neural network involved in sensory, affective, cognitive and behavioral aspects of nociception. These findings show that not only pharmacological but also psychological strategies for pain control can modulate the cerebral network involved in noxious perception.     

Central Projection of Pain Arising from Delayed Onset Muscle Soreness (DOMS) in Human Subjects

Delayed onset muscle soreness (DOMS) is a subacute pain state arising 24–48 hours after a bout of unaccustomed eccentric muscle contractions. Functional magnetic resonance imaging (fMRI) was used to examine the patterns of cortical activation arising during DOMS-related pain in the quadriceps muscle of healthy volunteers evoked by either voluntary contraction or physical stimulation. The painful movement or physical stimulation of the DOMS-affected thigh disclosed widespread activation in the primary somatosensory and motor (S1, M1) cortices, stretching far beyond the corresponding areas somatotopically related to contraction or physical stimulation of the thigh; activation also included a large area within the cingulate cortex encompassing posteroanterior regions and the cingulate motor area. Pain-related activations were also found in premotor (M2) areas, bilateral in the insular cortex and the thalamic nuclei. In contrast, movement of a DOMS-affected limb led also to activation in the ipsilateral anterior cerebellum, while DOMS-related pain evoked by physical stimulation devoid of limb movement did not.     

Transcranial flavoprotein fluorescence imaging of mouse cortical activity and plasticity

Endogenous fluorescence signals derived from mitochondria reflect activity-dependent changes in brain metabolism and may be exploited in functional brain imaging. Endogenous flavoprotein fluorescence imaging in mice is especially important because many genetically manipulated strains of mice are available and the transparent skull of mice allows transcranial fluorescence imaging of cortical activities. In the primary sensory areas of mice, cortical activities and experience-dependent plasticity have been investigated using transcranial fluorescence imaging. Furthermore, differential imaging, based on stimulus specificity of cortical areas, distinguished activities in higher visual areas around the primary visual cortex from those in primary visual cortex. The combination of transcranial fluorescence imaging with the suppression of cortical activities using photobleaching of flavoproteins is expected to aid in elucidating the roles of sensory cortices including higher areas in mice.