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Discrimination between active and passive head movements by macaque ventral and medial intraparietal cortex neurons. Abstract. An important prerequisite for effective motor action is the discrimination between active and passive body movements. Passive movements often require immediate reflexes, whereas active movements may demand suppression of the latter. The vestibular system maintains correct body and head posture in space through reflexes. Since vestibular inputs have been reported to be largely suppressed in the vestibular nuclei during active head movements, we investigated whether head movement- related signals in the primate parietal cortex, a brain region involved in self- motion perception, could support both reflex functions and self- movement behaviour. We employed a paradigm that made available direct comparison of neuronal discharge under active and passive movement conditions. In this study, we demonstrate that a population of intraparietal (VIP (ventral) and MIP (medial)) cortex neurons change their preferred directions during horizontal head rotations depending on whether animals have performed active movements, or if they were moved passively. Many SPM users have created tools for neuroimaging analyses that are based on SPM. You will find here a list of these tools classified between Toolboxes, Utilities. MR Imaging of the Temporal Stem: Anatomic Dissection Tractography of the Uncinate Fasciculus, Inferior Occipitofrontal Fasciculus, and Meyer’s Loop of. A brain-to-brain interface (BTBI) enabled a real-time transfer of behaviorally meaningful sensorimotor information between the brains of two rats. A Combined Mri And Histology Atlas Of The Rhesus Monkey Brain In Stereotaxic Coordinates PdfIn other neurons no such change occurred. A combination of these signals would provide differential information about the active or passive nature of an ongoing movement. Moreover, some neurons' responses clearly anticipated the upcoming active head movement, providing a possible basis for vestibular- related reflex suppression. Intraparietal vestibular neurons thus distinguish between active and passive head movements, and their responses differ substantially from those reported in brainstem vestibular neurons, regarding strength, timing, and direction selectivity. We suggest that the contextual firing characteristics of these neurons have far- reaching implications for the suppression of reflex movements during active movement, and for the representation of space during self- movement. The posterior parietal cortex has been thought for a long time to be involved in space perception, self- motion detection and navigation (Colby & Goldberg, 1. Swan, 2. 00. 1). In the present study, we examined the recently discovered vestibular signals in macaque intraparietal cortex neurons (Bremmer et al. Klam & Graf, 2. VIP), with reference to their responses to actively generated and passively imposed head movements. A distinction between active and passive movements is an important function for goal- directed movements without interference by reflex mechanisms, and to allow vital reflexes to happen when necessary. Furthermore, perceiving the external world as stable requires compensating for visual motion, and – more generally – sensory stimulation induced by self- movement. Recent studies of vestibular nuclei neurons during passive and active head movements in monkeys showed that vestibular signals were strongly attenuated by self- generated movements as early as the first vestibular projection neurons (Gdowski & Mc. Crea, 1. 99. 9; Mc. Crea et al. 1. 99. Roy & Cullen, 2. Cullen & Roy, 2. Khalsa et al. 1. 98. For instance, neurons could stop firing during active head movements, while during passive movements, they would transmit a head velocity signal. Furthermore, in the vestibular nuclei, neurons carrying eye and head movement- related signals have been found in a similar proportion as neurons that only signal head velocity, with no eye movement signals present (Gdowski & Mc. Crea, 1. 99. 9). The latter are thought to be part of the vestibulo- cortical relay. Vestibular thalamic and cortical units have been reported not to carry eye movement signals (Büttner et al. Magnin & Fuchs, 1. Grüsser et al. 1. We were therefore interested in the functional properties of cortical neurons that carry signals about head movements. This work extends our previous reports on vestibular responses in VIP (Bremmer et al. Klam & Graf, 2. Duhamel et al. 1. Bremmer et al. 2. Zhang et al. 2. 00. Preliminary accounts have been presented in brief, earlier (Klam & Graf, 2. Methods. General. Extracellular recordings were made in the left hemispheres (Fig. A) of two macaque monkeys, one male rhesus (Macaca mulatta), and one female fascicularis monkey (Macaca fascicularis). The animals were purpose- bred and purchased from authorized suppliers. Animal care (housing, nourishment, veterinary consultations, surgical procedures, postoperative care, daily care) conformed to French government regulations (Ministries of Agriculture and Research, CNRS: approval no. European Union standards (European Communities Council Directive 8. EEC). Recording sites and active–passive replay paradigm. Animals were in experimental sessions, usually on a daily basis during work days, for a duration of 3–4 h per day. No experiments were scheduled during weekends. The animal facilities were adjacent to the laboratory, thus minimizing travel time for bringing the animals into the experimental set- up. Monkey 1 was used for 1. Naturally, there was some down- time in the experimental schedule for the animals to recover for more than just the weekends. Surgical procedures. All surgical procedures were performed aseptically under general anaesthesia initiated with ketamine (2. Valium (diazepam 1. Subsequently, venous access was established. Deep general anaesthesia was maintained via continuous infusion of Rapinovet (propofol 1. The animals were intubated, but typically respired spontaneously. An ECG was recorded routinely. For the surgical procedures, the monkeys' heads were fixed in a stereotaxic head- holder via ear bars and a mouth clamp. At first, sclera- concentric coils made of three turns of Teflon- coated silver wire were implanted in each eye. The ends were led under the skin to the top of the head and soldered to previously manufactured plugs. These were later anchored with dental acrylic to the skull. The skin over the skull was opened and small self- tapping stainless- steel screws were threaded into the bone. Onto these, an earth- vertical head- holding device was anchored with dental acrylic. At the coordinates of the intraparietal sulcus (centred at P3. L1. 2), a trepan hole was made into the skull without opening the underlying dura. A stainless steel cylinder was mounted over the opening. Into this cylinder, a Teflon grid for electrode placement was inserted, and a hydraulic motor- driven microdrive (Narishige) was mounted during recording sessions. The grid allowed reproducible electrode penetrations with a 5. Postoperative care involved local application of neomycin/hydrocortisone ophthalmic cream, administration of antibiotics (penicillin 7. During subsequent routine surgical procedures (e. Animal training. Head- fixed animals were initially trained to fixate a small spot of light within a narrow target window (2 deg × 2 deg) for a minimum of 3. The light spot could be kept stationary in darkness and in light to monitor a given neuron's resting activity. To determine a neuron's eye position sensitivity, the spot was moved in random order into nine different locations on a tangent screen (Bremmer et al. The spot could also be moved to test smooth pursuit sensitivity. Pursuit eye movements were only tested in a subset of neurons with a step- ramp paradigm (step size 1. The animals' heads were fastened in a specialized head- holder system that allowed free head movements in the stereotaxic frame of reference (Fig. B and C). The head- holder was constructed to allow horizontal head movements (vertical axis rotations) once a set screw was released, but no vertical excursions. The set screw had a very short grading, and was operated from behind the animal. Thus, there was minimal to no disturbance for the animal when switching from head- fixed to head- free, and vice versa. Once the head was freed, the animals were allowed to make spontaneous head movements. From the combined signals, head, eye and gaze information could be derived. Each animal was allowed an adjustment period to find its ‘comfort point’ for horizontal head rotation on the holder's horizontal arm along the naso- occipital axis. Such a procedure was necessary since the head post needed to be placed over the frontal bone in order not to interfere with the chamber implant over the parietal cortex. Our previous biomechanical studies had indicated the exact rotation axis for horizontal head movements within the atlanto- axial joint (C1/C2) (Vidal et al. Graf et al. 1. 99. Smooth and friction- free operation of the moving parts of the head- holder was ensured by enclosed ball bearings. Recordings. Single cells were recorded extracellularly with glass- coated tungsten microelectrodes (F. Haer) in areas VIP and MIP (medial intraparietal area) of the two left hemispheres of the two monkeys (for details see Bremmer et al. Klam & Graf, 2. The animals were awake, and performed several oculomotor tasks. Neurons were classified as being located in area VIP on the basis of the recording sites and depth within the intraparietal sulcus, and with respect to their response properties (Colby & Duhamel, 1. Colby et al. 1. 99. Schaafsma & Duysens, 1. Schaafsma et al. 1. Duhamel et al. 1. Neurons in MIP were characterized by absent or low visual sensitivity and strong somatosensory responses located on the fingers, hands and forearms (Klam & Graf, 2. In a typical recording session, the passage of the electrode from the MIP into the VIP was marked by a distinct change in background and resting activity of the recorded neuronal elements (Klam & Graf, 2. Eye movements were recorded with the magnetic search coil method, head movements with a head- holder- mounted potentiometer. Previous tests had shown that the eye movement signal remained linear within the physiological working range of the monkey's eye–head movements (see Figs 2 and 3). Neuronal signals were sampled at 1. Hz, and eye and head position at 2. Clinical Medicine Courses, Textbooks, Lectures, Publications, Technical Reports, Videos, Cases, Grand Rounds, etc. Theriogenology Courses. THERIOGENOLOGY (VMED 5. D. L. Paccamonti & S. K. Lyle (Theriogenology). D. P. Beehan, M. G. Welborn & A. J. Fuselier (Veterinary Clinical Science). Contributed by B. E. Eilts (Retired). Veterinary Teaching Hospital. School of Veterinary Medicine. Louisiana State University. Baton Rouge. Louisiana. Multimedia Theriogenology Course (Text, Images & Audio/Sound). Theriogenology. ".. Examples of "Theriogenology" Course Subject Categories include. Semen Analysis and Cooled, Chilled Semen Preparation. Equine Theriogenology. Canine Theriogenology. Feline Theriogenology. Bovine Theriogenology. Swine Theriogenology. 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