Preparation for the in vivo recording of neuronal responses in the visual cortex of anaesthetised marmosets (Callithrix jacchus).

The marmoset is becoming an important model for studies of primate vision, due to factors such as its small body size, lissencephalic brain, short gestational period and rapid postnatal development. For many studies of visual physiology (including single-cell recordings), it is a requirement that the animal is maintained under anaesthesia and neuromuscular block in order to ensure ocular stability. However, maintaining such a small animal (290-400 g) in good physiological condition for long periods requires expert attention. This becomes particularly important in the case of recordings from visual association cortex, where neuronal responses are known to be highly sensitive to factors such as the type and dose of anaesthetic, and the animal's physiological balance. The present protocol summarises our laboratory's experience over the last decade in developing a preparation for the study of marmoset visual cortex. It allows excellent recording from extrastriate areas for periods of at least 48 h, including the continuous study of isolated single cells for several hours.

[1]  H. Abe,et al.  The Effects of Anesthetics on Cortical Spreading Depression Elicitation and c-fos Expression in Rats , 2001, Journal of neurosurgical anesthesiology.

[2]  M. Rosa,et al.  Visual areas in lateral and ventral extrastriate cortices of the marmoset monkey , 2000, The Journal of comparative neurology.

[3]  W. B. Spatz,et al.  Distribution of cytochrome oxidase and parvalbumin in the primary visual cortex of the adult and neonate monkey, Callithrix jacchus , 1994, The Journal of comparative neurology.

[4]  E Sugaya,et al.  Neuronal and glial activity during spreading depression in cerebral cortex of cat. , 1975, Journal of neurophysiology.

[5]  A. A. Leão,et al.  SPREADING DEPRESSION OF ACTIVITY IN THE CEREBRAL CORTEX , 1944 .

[6]  Paul R. Martin,et al.  Temporal contrast sensitivity in the lateral geniculate nucleus of a New World monkey, the marmoset Callithrix jacchus , 1999, The Journal of physiology.

[7]  H. Grady Rylander,et al.  Maintaining the cornea and the general physiological environment in visual neurophysiology experiments , 2001, Journal of Neuroscience Methods.

[8]  N. Brennan,et al.  Corneal pathophysiology with contact lens wear. , 1990, Survey of ophthalmology.

[9]  Charles Nicholson,et al.  Perspectives on spreading depression , 2000, Brain Research Reviews.

[10]  J R Wolff,et al.  Pre‐ and postnatal development of the primary visual cortex of the common marmoset. II. Formation, remodelling, and elimination of synapses as overlapping processes , 1993, The Journal of comparative neurology.

[11]  T. Poole UFAW Handbook on the Care and Management of Laboratory Animals , 1987 .

[12]  P. Lennie,et al.  Chromatic mechanisms in striate cortex of macaque , 1990, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[13]  D. V. van Essen,et al.  Response modulation by texture surround in primate area V1: Correlates of “popout” under anesthesia , 1999, Visual Neuroscience.

[14]  J. Jones,et al.  Effects of a low concentration of isoflurane on contrast sensitivity in volunteers. , 1998, British journal of anaesthesia.

[15]  Marcello G P Rosa,et al.  Physiological responses of New World monkey V1 neurons to stimuli defined by coherent motion. , 2002, Cerebral cortex.

[16]  J R Wolff,et al.  Pre‐ and postnatal development of the primary visual cortex of the common marmoset. I. A changing space for synaptogenesis , 1993, The Journal of comparative neurology.

[17]  G. Elston,et al.  Visual Responses of Neurons in the Middle Temporal Area of New World Monkeys after Lesions of Striate Cortex , 2000, The Journal of Neuroscience.

[18]  C Blakemore,et al.  Functional architecture of area 17 in normal and monocularly deprived marmosets (Callithrix jacchus) , 1996, Visual Neuroscience.

[19]  J. Bourne,et al.  Novel method of monitoring electroencephalography at the site of microdialysis during chemically evoked seizures in a freely moving animal , 2000, Journal of Neuroscience Methods.

[20]  P A Salin,et al.  Response selectivity of neurons in area MT of the macaque monkey during reversible inactivation of area V1. , 1992, Journal of neurophysiology.

[21]  G M Murray,et al.  Parallel processing in cerebral cortex of the marmoset monkey: effect of reversible SI inactivation on tactile responses in SII. , 1996, Journal of neurophysiology.

[22]  M G Rosa,et al.  Visuotopic organisation of striate cortex in the marmoset monkey (Callithrix jacchus) , 1996, The Journal of comparative neurology.

[23]  A Grinvald,et al.  Optical imaging reveals the functional architecture of neurons processing shape and motion in owl monkey area MT , 1994, Proceedings of the Royal Society of London. Series B: Biological Sciences.