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Brain Imaging Technologies - Coursework Example

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The paper "Brain Imaging Technologies" brings to light Positron Emission Tomography scanning, a sophisticated imaging technique alongside functional Magnetic Resonance Imaging technique, event-related potential, single-cell recording, visual-spatial sketchpad, and central executive…
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Brain Imaging Technologies
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BRAIN IMAGING TECHNOLOGIES SUBMITTED INTRODUCTION Brain imaging technologies are used to measure brain activity. This paper brings to light Positron Emission Tomography (PET) scanning, a sophisticated imaging technique alongside functional Magnetic Resonance Imaging (MRI) technique, event related potential, single cell recording, visual-spatial sketchpad and central executive. The capability to image the human body, equally to spot disease and direct surgery, has become cardinal to the implementation of medicine. In the resulting time, radiology has burgeoned to cover the use of many faces of electromagnetic radiation in making increasingly dominant diagnostic images of the body and diseases. The variety of energies and specialties like radiology, medical physics, nuclear pharmacy, etc has led to hospitals and university research centers being called diagnostic imaging or radiology or the science of radiology. No name yet worked out is wholly satisfactory in the countenance of the vivid changes which have occurred, mainly in the last three or four decades. (Kuhn, 2004) The power of contemporary computers to allow the speedy display of sectional images of the body by means of technologies such as ultrasound, computed tomography scan, single-photon emission topography, positron emission topography or magnetic resonance imaging has been cardinal to the upbringing of the latest technologies. Nevertheless, an equally great change has been that encompassing the move of medical imaging from the laboratory to the living room. Many Decades ago what was then radiological science poked a restricted series of diagnostic information to a referring medical doctor apprehensive to resolve diagnostic ambiguity between the diseases potentially able to report for a patient's indicators. In the beginning of the this century, imaging technology is used not only to spot the abrasion, and to do so more effectively, but to direct the needle used in its biopsy; not only to recognize a blocked vessel but to guide its dilatation as well. FMRI AND PET Functional Magnetic Resonance Imaging is based on the boost in blood flow to the local vasculature that comes along neural activity in the brain. This result in a consequent local drop in deoxyhemoglobin because the augmentation in blood flow occurs without an amplification of similar magnitude in oxygen extraction. Thus, deoxyhemoglobin is every now and then is known as a contrast enhancing agent, and serves as the source of the signal for fMRI. Functional activity of the brain obtained from the magnetic resonance pointer has verified known anatomically dissimilar processing regions in the visual cortex, the motor cortex, and Broca's area of speech and language-related activities. Further, speedily rising bodies of research document communicate to findings between fMRI and usual electro-physiological methods to localize explicit functions of the human brain (Romanelli, 2004). Consequently, the number of medical and research centers with fMRI capabilities and investigational programs continues to shoot up. The major returns to fMRI as a technique to image brain activity related to a particular objective or sensory process says the the signal does not need doses of radioactive isotopes, the total scan time needed can be very less, i.e., on the order of 1.5 to 2.0 minutes per run (depending on the paradigm), and the in-plane resolution of the functional image is generally about 1.5 x 1.5 mm although resolutions less than 1 mm are likely. To put these pros in standpoint, functional images obtained by the earlier method of positron emission tomography, require doses of radioactive isotopes, multiple acquisitions, and therefore, longer imaging times. Additionally, the anticipated resolution of positron emission tomography images is much larger than the common functional magnetic resonance imaging pixel size. In addition, positron emission tomography usually requires that numerous individual brain images are joined in order to obtain a dependable signal. As a result, information on a single patient is cooperated and limited to a definite number of imaging gatherings. Even though these restrictions may dish up many neuroscience applications, they are not highly suitable to aid in a neurosurgical or treatment plan for a specific person. (Donoghue, 1998) Positron emission tomography can assist physicians efficiently locate the basis of cancer. This is probable because many cancer cells are extremely metabolic and thus synthesize the radioactive glucose that is induced in the patient prior to the test. The areas of high glucose uptake are severely displayed in the scan imagery, as opposed to the imagery of CT or Magnetic Resonance Imaging, which cannot detect lively, doable tumors. If cancer is diagnosed in the initial stages, it can often be cured. A positron emission tomography scan can be utilized in premature diagnosis, assisting doctors in formulating the best method for treatment. A whole body positron emission tomography scan might detect whether cancer is isolated to one specific area or has spread to other organs before a treatment route is determined. EVENT_RELATED POTENTIAL Event-Related Potentials are little voltage oscillations as a result from stirred up neural activity. These electrical signal changes are reflections from scalp recordings by computer recording periods of Electroencephalography time-locked to recurring of sensory, cognitive, or motor events. The impulsive background Electroencephalography fluctuations, which are arbitrary relative to the stimuli occurrence, are left behind, leaving the event-related brain potentials. These electrical signals mirror only that activity which is every time related to the stimulus processing in a time-locked way. The event-related potential thus reflects, with high temporal motion, the patterns of neuron activity invoked by a stimulus. Because of their elevated temporal resolution, Event-related potentials offer exclusive and vital timing information about brain processing. Neural operations, like those included in perception, selective attention, language processing, and memory, advance over time intervals in the order of tens of milliseconds. The majority of other functional imaging methods require the combining stimulated brain activity over quite a few seconds and are hence not able to detain the time course of these processes (Kuhn, 2004). Event-related potential recordings, however, provide a millisecond-by-millisecond reflection of stirred brain activity. For this reason, Event-related potentials are an ideal technique for observing the time characteristic of both normal and irregular cognitive neuro-processes. Then again, Event-related potential data offer not as much of accurate time information compared to positron emission tomography or functional magnetic resonance imaging, which is fairly short of fine temporal resolution. Consequently, event-related potential represent the normal balance of positron emission tomography and functional Magnetic Resonance Imaging to study cognitive processes. Whereas positron emission tomography and functional Magnetic Resonance Imaging are able to localize areas of activity throughout a specific neuro-task, Event-related potentials can help in defining the time course of these activations. In a medical environment, the temporal resolution of Event-related potentials is handy in pointing out at what level along the sensory pathways a lesion is located. Visual Event-related potentials assist the initial spotting of multiple areas earlier than any structural irregularity pattern is detected. Event-related potentials are also used to observe exhausted patients to evaluate the operation of important areas in the brainstem. SINGLE-CELL RECORDING: Single-cell recording is a technique used in research to scrutinize voltage or current fluctuations in a cell. An electrode is placed into a neuron and measures electrical charges in that neuron. It is a technique used in research to observe changes in voltage or current in a neuron. In this method, the subject which is usually under the influence of anesthesia has a microelectrode put into its skull and then into a neuron in the area of the neural region that is of interest. The electrode quantifies the change in activity when the neuron reaches its action potential. This practice is typically synchronized with some sort of stimuli. It is similar to a probe that could be put into a single neuron in a specific area of the visual cortex of the subject. The subject is then faced with a sequence of lights in diverse directions on a dark screen. Whatever direction of light is being tested at the time the electrode signals a variation in voltage. Single cell recording has the best resolution of all brain imaging techniques. It provides more information about the activities of a few neurons. This technique allows the recordings of up to fifty cells, and with this method it is also possible to track the activity of a neuron over time. VISIO-SPATIAL SKETCHPAD The visio-spatial sketchpad is for use to hold visual or spatial information in short-term memory load, where it can be processed. It is analogous to the aural system and really, there are proposals that the visio-spatial sketchpad is also made up of two dissimilar small systems, one being visual and the other spatial. Information might come into the system from the outside world via iconic store or it can come from the long term memory area. Current debates on visio-spatial operational memory have put forward that this part of the system may add in a visual buffer the function of what is to hold visio-spatial information very inertly. Experiential studies of visual interference with information contained in a visio-spatial part of the whole system have given in somewhat vague results. However prior studies have pointed out that visio-spatial processing can be disturbed greatly by unreceptive revelation to unrelated visual material in a way similar to the disturbance of serial verbal recollections by revelation to unrelated speech. According to a model of working memory, temporary storage and manipulation of task-relevant information is achieved via a modular structure of at least three functional subsystems (Wichmann, 1996). Verbal speech-based information is treated with by the articulator loop, whilst visio-spatial material is processed and stored using a specialized system known as the visio-spatial sketchpad. These sub-systems are thought to be installed and coordinated by a restricted capacity centralized executive. Till rather in recent times, inquiry into the uniqueness of working memory was converged primarily upon the workings of the articulatory loop. However, over the last few years particular attention has been devoted to the characteristics of the visio-spatial sketchpad. There is now a huge body of facts supporting the notion of a visio-spatial sketchpad that inertly has images which may be removed by unrelated visual input, and worked on by some spatial attentional device (Papavassiliou et al 2004). Fiasco of visio-spatial operations by synchronized spatial movements has been widely researched on. A diversity of visio-spatial experiments reveal intervention effects from spatial tracking (Papavassiliou et al, 2004), limb movements, if intentional or not and eye movements. It has been disputed upon that active spatial processing might be strengthened by some thing relied on spatial movement, with similarities drawn between the role of articulation in verbal rehearsal, and movement in spatial rehearsal (Romanelli, 2004). Hence, just as articulation of inappropriate verbal stuff may restrain task-relevant verbal rehearsal, it is recommended that the harmful effects of spatial movements can be observed as a form of spatial suppression. The central executive administers memory strengthening, and handles cognitive load. The central executive is the slightest well hypothesized part of the system. It can be taken of as an attentional control mechanism that harmonizes the actions of the sub- systems. CONCLUSIVE REMARKS: Much of the facts for this system were made by Baddeley and Hitch in a long and tiring series of laboratory work. There was a good finding that things like listening to American football commentary on the radio impaired driving ability. This takes us to that there should exist a control mechanism that is getting overtaxed by listening to and understanding the football game. Intelligence must be closely related to these systems, since much of intelligence could be explained on the basis of verbal fluency (the phonological loop), visiospatial skills (the visiospatial sketchpad), or logical processing (the central executive) (Bergman, 2002). References Kuhn, A. A. et al. Event-related beta desynchronization in human subthalamic nucleus correlates with motor performance. Brain 127, 735-746 (2004). Donoghue, J. P., Sanes, J. N., Hatsopoulos, N. G. & Gaal, G. Neural discharge and local field potential oscillations in primate motor cortex during voluntary movements. J. Neurophysiol. 79, 159-173 (1998). Wichmann, T. & DeLong, M. Functional and pathophysiological models. Curr. Opin. Neurobiol. 6, 751-758 (1996). Bergman, H., Wichmann, T. & DeLong, M. R. Reversal experiment by lesions of the subthalamic nucleus. Science 249, 1436-1438 (1990). Papavassiliou, E. et al. Thalamic deep brain stimulation for essential tremor: relation of lead location to outcome. Neurosurgery 54, 1120-1129 (2004). Romanelli, P. et al. Microelectrode recording revealing a somatotopic body map in the subthalamic nucleus in humans. J. Neurosurg. 100, 611-618 (2004). MacMillan, M. L., Dostrovsky, J. O., Lozano, A. M. & Hutchison, W. D. Involvement of human thalamic neurons in internally and externally generated movements. J. Neurophysiol. 91, 1085-1090 (2004). Bergman, H. & Deuschl, G. Pathophysiology: from clinical neurology to basic neuroscience and back. Mov. Disord. 17 (Suppl. 3), S28-S40 (2002) Read More
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