Max Bennett (scientist)

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ISBN 0521084636
  • Optimising Research and Development in Australia (1987) Publisher: Australian Academy of Science; ISBN   0858471388
  • The Idea of Consciousness: Synapses and the Mind (1997) Publisher: Harwood Academic; ISBN   9057022036
  • History of the Synapse (2001) Publisher: Harwood Academic; ISBN   9058231321
  • Philosophical Foundations of Neuroscience (2003) Publisher: Blackwell; ISBN   1 4051 0855 X(with Peter Hacker)
  • Neuroscience and Philosophy : Brain, Mind and Language (2006) Publisher: Columbia University Press (with Daniel Dennett, John Searle and Peter Hacker)
  • History of Cognitive Neuroscience (2008) Publisher: Wiley/Blackwell; ISBN   9781405181822 (with Peter Hacker)
  • Virginia Woolf and Neuropsychiatry (2013) Publisher: Springer; ISBN   9789400757486
  • Interviews

    Bennett, Max; Blythe, Max (1996). "Professor Max Bennett FAA in interview with Dr Max Blythe". Oxford Brookes University. doi:10.24384/000147.{{cite journal}}: Cite journal requires |journal= (help)

    Related Research Articles

    <span class="mw-page-title-main">Neuron</span> Electrically excitable cell found in the nervous system of animals

    Within a nervous system, a neuron, neurone, or nerve cell is an electrically excitable cell that fires electric signals called action potentials across a neural network. Neurons communicate with other cells via synapses, which are specialized connections that commonly use minute amounts of chemical neurotransmitters to pass the electric signal from the presynaptic neuron to the target cell through the synaptic gap.

    <span class="mw-page-title-main">Nervous system</span> Part of an animal that coordinates actions and senses

    In biology, the nervous system is the highly complex part of an animal that coordinates its actions and sensory information by transmitting signals to and from different parts of its body. The nervous system detects environmental changes that impact the body, then works in tandem with the endocrine system to respond to such events. Nervous tissue first arose in wormlike organisms about 550 to 600 million years ago. In vertebrates it consists of two main parts, the central nervous system (CNS) and the peripheral nervous system (PNS). The CNS consists of the brain and spinal cord. The PNS consists mainly of nerves, which are enclosed bundles of the long fibers, or axons, that connect the CNS to every other part of the body. Nerves that transmit signals from the brain are called motor nerves or efferent nerves, while those nerves that transmit information from the body to the CNS are called sensory nerves or afferent. Spinal nerves are mixed nerves that serve both functions. The PNS is divided into three separate subsystems, the somatic, autonomic, and enteric nervous systems. Somatic nerves mediate voluntary movement. The autonomic nervous system is further subdivided into the sympathetic and the parasympathetic nervous systems. The sympathetic nervous system is activated in cases of emergencies to mobilize energy, while the parasympathetic nervous system is activated when organisms are in a relaxed state. The enteric nervous system functions to control the gastrointestinal system. Both autonomic and enteric nervous systems function involuntarily. Nerves that exit from the cranium are called cranial nerves while those exiting from the spinal cord are called spinal nerves.

    <span class="mw-page-title-main">Chemical synapse</span> Biological junctions through which neurons signals can be sent

    Chemical synapses are biological junctions through which neurons' signals can be sent to each other and to non-neuronal cells such as those in muscles or glands. Chemical synapses allow neurons to form circuits within the central nervous system. They are crucial to the biological computations that underlie perception and thought. They allow the nervous system to connect to and control other systems of the body.

    <span class="mw-page-title-main">Motor neuron</span> Nerve cell sending impulse to muscle

    A motor neuron is a neuron whose cell body is located in the motor cortex, brainstem or the spinal cord, and whose axon (fiber) projects to the spinal cord or outside of the spinal cord to directly or indirectly control effector organs, mainly muscles and glands. There are two types of motor neuron – upper motor neurons and lower motor neurons. Axons from upper motor neurons synapse onto interneurons in the spinal cord and occasionally directly onto lower motor neurons. The axons from the lower motor neurons are efferent nerve fibers that carry signals from the spinal cord to the effectors. Types of lower motor neurons are alpha motor neurons, beta motor neurons, and gamma motor neurons.

    <span class="mw-page-title-main">Bernard Katz</span> German-British biophysicist (1911–2003)

    Sir Bernard Katz, FRS was a German-born British physician and biophysicist, noted for his work on nerve physiology; specifically, for his work on synaptic transmission at the nerve-muscle junction. He shared the Nobel Prize in physiology or medicine in 1970 with Julius Axelrod and Ulf von Euler. He was made a Knight Bachelor in 1969.

    <span class="mw-page-title-main">Neurotransmitter receptor</span> Type of protein

    A neurotransmitter receptor is a membrane receptor protein that is activated by a neurotransmitter. Chemicals on the outside of the cell, such as a neurotransmitter, can bump into the cell's membrane, in which there are receptors. If a neurotransmitter bumps into its corresponding receptor, they will bind and can trigger other events to occur inside the cell. Therefore, a membrane receptor is part of the molecular machinery that allows cells to communicate with one another. A neurotransmitter receptor is a class of receptors that specifically binds with neurotransmitters as opposed to other molecules.

    <span class="mw-page-title-main">Electrical synapse</span> Type of connection between neurons

    An electrical synapse is a mechanical and electrically conductive synapse, a functional junction between two neighboring neurons. The synapse is formed at a narrow gap between the pre- and postsynaptic neurons known as a gap junction. At gap junctions, such cells approach within about 3.8 nm of each other, a much shorter distance than the 20- to 40-nanometer distance that separates cells at a chemical synapse. In many animals, electrical synapse-based systems co-exist with chemical synapses.

    <span class="mw-page-title-main">Neuroeffector junction</span> Site where a motor neuron releases a neurotransmitter to affect a target cell

    A neuroeffector junction is a site where a motor neuron releases a neurotransmitter to affect a target—non-neuronal—cell. This junction functions like a synapse. However, unlike most neurons, somatic efferent motor neurons innervate skeletal muscle, and are always excitatory. Visceral efferent neurons innervate smooth muscle, cardiac muscle, and glands, and have the ability to be either excitatory or inhibitory in function. Neuroeffector junctions are known as neuromuscular junctions when the target cell is a muscle fiber.

    <span class="mw-page-title-main">Neuromuscular junction</span> Junction between the axon of a motor neuron and a muscle fiber

    A neuromuscular junction is a chemical synapse between a motor neuron and a muscle fiber.

    <span class="mw-page-title-main">Synaptic vesicle</span> Neurotransmitters that are released at the synapse

    In a neuron, synaptic vesicles store various neurotransmitters that are released at the synapse. The release is regulated by a voltage-dependent calcium channel. Vesicles are essential for propagating nerve impulses between neurons and are constantly recreated by the cell. The area in the axon that holds groups of vesicles is an axon terminal or "terminal bouton". Up to 130 vesicles can be released per bouton over a ten-minute period of stimulation at 0.2 Hz. In the visual cortex of the human brain, synaptic vesicles have an average diameter of 39.5 nanometers (nm) with a standard deviation of 5.1 nm.

    <span class="mw-page-title-main">Rodolfo Llinás</span> Colombian neuroscientist (born 1934)

    Rodolfo Llinás Riascos is a Colombian and American neuroscientist. He is currently the Thomas and Suzanne Murphy Professor of Neuroscience and Chairman Emeritus of the Department of Physiology & Neuroscience at the NYU School of Medicine. Llinás has published over 800 scientific articles.

    <span class="mw-page-title-main">Dale's principle</span> Principle in neuroscience

    In neuroscience, Dale's principle is a rule attributed to the English neuroscientist Henry Hallett Dale. The principle basically states that a neuron performs the same chemical action at all of its synaptic connections to other cells, regardless of the identity of the target cell. However, there has been disagreement about the precise wording.

    <span class="mw-page-title-main">Neuron doctrine</span>

    The neuron doctrine is the concept that the nervous system is made up of discrete individual cells, a discovery due to decisive neuro-anatomical work of Santiago Ramón y Cajal and later presented by, among others, H. Waldeyer-Hartz. The term neuron was itself coined by Waldeyer as a way of identifying the cells in question. The neuron doctrine, as it became known, served to position neurons as special cases under the broader cell theory evolved some decades earlier. He appropriated the concept not from his own research but from the disparate observation of the histological work of Albert von Kölliker, Camillo Golgi, Franz Nissl, Santiago Ramón y Cajal, Auguste Forel and others.

    Muscle weakness is a lack of muscle strength. Its causes are many and can be divided into conditions that have either true or perceived muscle weakness. True muscle weakness is a primary symptom of a variety of skeletal muscle diseases, including muscular dystrophy and inflammatory myopathy. It occurs in neuromuscular junction disorders, such as myasthenia gravis. Muscle weakness can also be caused by low levels of potassium and other electrolytes within muscle cells. It can be temporary or long-lasting. The term myasthenia is from my- from Greek μυο meaning "muscle" + -asthenia ἀσθένεια meaning "weakness".

    Neuromodulation is the physiological process by which a given neuron uses one or more chemicals to regulate diverse populations of neurons. Neuromodulators typically bind to metabotropic, G-protein coupled receptors (GPCRs) to initiate a second messenger signaling cascade that induces a broad, long-lasting signal. This modulation can last for hundreds of milliseconds to several minutes. Some of the effects of neuromodulators include: altering intrinsic firing activity, increasing or decreasing voltage-dependent currents, altering synaptic efficacy, increasing bursting activity and reconfigurating synaptic connectivity.

    From the ancient Egyptian mummifications to 18th-century scientific research on "globules" and neurons, there is evidence of neuroscience practice throughout the early periods of history. The early civilizations lacked adequate means to obtain knowledge about the human brain. Their assumptions about the inner workings of the mind, therefore, were not accurate. Early views on the function of the brain regarded it to be a form of "cranial stuffing" of sorts. In ancient Egypt, from the late Middle Kingdom onwards, in preparation for mummification, the brain was regularly removed, for it was the heart that was assumed to be the seat of intelligence. According to Herodotus, during the first step of mummification: "The most perfect practice is to extract as much of the brain as possible with an iron hook, and what the hook cannot reach is mixed with drugs." Over the next five thousand years, this view came to be reversed; the brain is now known to be the seat of intelligence, although colloquial variations of the former remain as in "memorizing something by heart".

    <span class="mw-page-title-main">Calyx of Held</span>

    The Calyx of Held is a particularly large synapse in the mammalian auditory central nervous system, so named after Hans Held who first described it in his 1893 article Die centrale Gehörleitung because of its resemblance to the calyx of a flower. Globular bushy cells in the anteroventral cochlear nucleus (AVCN) send axons to the contralateral medial nucleus of the trapezoid body (MNTB), where they synapse via these calyces on MNTB principal cells. These principal cells then project to the ipsilateral lateral superior olive (LSO), where they inhibit postsynaptic neurons and provide a basis for interaural level detection (ILD), required for high frequency sound localization. This synapse has been described as the largest in the brain.

    <span class="mw-page-title-main">Axon terminal</span> Nerve fiber part

    Axon terminals are distal terminations of the branches of an axon. An axon, also called a nerve fiber, is a long, slender projection of a nerve cell that conducts electrical impulses called action potentials away from the neuron's cell body in order to transmit those impulses to other neurons, muscle cells or glands. In the central nervous system, most presynaptic terminals are actually formed along the axons, not at their ends.

    Cellular neuroscience is a branch of neuroscience concerned with the study of neurons at a cellular level. This includes morphology and physiological properties of single neurons. Several techniques such as intracellular recording, patch-clamp, and voltage-clamp technique, pharmacology, confocal imaging, molecular biology, two photon laser scanning microscopy and Ca2+ imaging have been used to study activity at the cellular level. Cellular neuroscience examines the various types of neurons, the functions of different neurons, the influence of neurons upon each other, and how neurons work together.

    <span class="mw-page-title-main">Thomas C. Südhof</span> German-American biochemist

    Thomas Christian Südhof, ForMemRS, is a German-American biochemist known for his study of synaptic transmission. Currently, he is a professor in the school of medicine in the department of molecular and cellular physiology, and by courtesy in neurology, and in psychiatry and behavioral sciences at Stanford University.

    References

    1. "Australian Academy of Science interview with Max Bennett, 1996". Archived from the original on 14 July 2014. Retrieved 17 June 2014.
    2. Bennett, M.R., Burnstock, G. & Holman, M.E. (1966). Transmission from intramural inhibitory nerves to the smooth muscle of the guinea-pig taenia coli. J. Physiol. 182: 541-558. This work showed that another transmitter other than noradrenaline or acetylcholine exists in the peripheral nervous system.
    3. Brain, K.L. & Bennett, M.R. (1997). Calcium in sympathetic varicosities of mouse vas deferens during facilitation, augmentation and autoinhibition. J. Physiol. 502: 521-536. First to show that calcium changes in a nerve terminal directly related to synaptic efficacy.
    4. Bennett, M.R., Farnell, L. & Gibson, W.G. (2000) The probability of quantal secretion within an array of calcium channels of an active zone. Biophys. J. 78: 2222-2240. First realistic Monte Carlo account of calcium changes and transmitter release.
    5. Hansen, M.A., Balcar, V.J., Barden, J.A. & Bennett, M.R. (1998). The distribution of single P2x1 -receptor clusters on smooth muscle cells in relation to nerve varicosities in the rat urinary bladder. J. Neurocytol. 27: 529-539. Showed for the first time the relationship between single synapses and transmitter receptors in the postganglionic nervous system.
    6. Dutton, J.l., Poronnik, P., Li, G.H., Holding, C.A., Worthington, R.A., Vandenberg, R.J., Cook, D.I., Barden, J.A. & Bennett, M.R. (2000) P2X1 receptor membrane redistribution and down-regulation visualized by using receptor-coupled green fluorescent protein chimeras. Neuropharmacology 39: 2054-2066. First description of changes in distribution of agonist excited receptors in membranes in real time.
    7. Bennett, M.R. (1972). Autonomic Neuromuscular Transmission. Monograph of the Physiological Society No. 30, Cambridge University Press. This monograph established the prevailing paradigm of the structure and function of autonomic junctions.
    8. Bennett, M.R. (1967). The effect of cations on the electrical properties of the smooth muscle cells of the guinea-pig vas deferens. J. Physiol. 190: 465- 479. First proof that action potentials can be due to the influx of calcium ions.
    9. Bennett, M.R. & Pettigrew, A.G. (1976). The formation of neuromuscular synapses. Cold Spring Harb. Symp. Quant. Biol. 40: 409-424. This work established the prevailing paradigm of how synapses are formed during development and regeneration.
    10. Macleod, G.T., Dickens, P.A. & Bennett, M.R. (2001). Formation and function of synapses with respect to Schwann cells at the end of motor-nerve terminal branches on mature amphibian (Bufo marinus) muscle. J. Neurosci. 21: 2380-2392 (cover story). Showed that the mature intact nerve terminal continually makes and regresses synapses under the influence of the ensheathing glial cells.
    11. Bennett, M.R., Buljan, V., Farnell, L., Gibson, W. (2007). Purinergic junctional transmission and propagation of calcium waves in cultured spinal cord microglia networks. Purinergic Sig. 4: 47-59. This work showed for the first time that microglial cells, the most dynamic cell in the brain, act as an interface between the neural and immune systems by propagating calcium waves using purines as transmitters.
    12. Kassem MS, Lagopoulos J, Stait-Gardner T, Price WS, Chohan TW, Arnold JC, Hatton SN, Bennett MR. Stress-induced grey matter loss determined by MRI is primarily due to loss of dendrites and their synapses. Mol Neurobiol. 2013 Apr;47(2):645-61. Establishes for the first time the cellular basis of grey matter changes in the brain, determined by MRI.
    13. Hyder F, Rothman DL, Bennett MR. Cortical energy demands of signaling and nonsignaling components in brain are conserved across mammalian species and activity levels. Proc Natl Acad Sci U S A. 2013 Feb 26;110(9):3549-54. Shows that the energy required to maintain a synapse-initiated impulse in a neuron remains the same over different behavioural states and species.
    14. Bennett MR, Farnell L, Gibson WG. Fiber pathway pathology, synapse loss and decline of cortical function in schizophrenia. PLoS One. 2013 Apr 8;8(4). Indicates that changes in the energy expended in particular areas of the brain, and therefore impulse activity there, can be quantitatively explained as due to changes in the integrity of axons joining these areas.
    15. "Guide to the Records of the Department of Anthropology, 1901-[ongoing]". oac.cdlib.org.
    16. "Teachers Notes - Professor Max Bennett | Australian Academy of Science". www.science.org.au.
    17. "Document - Gale Academic OneFile". go.gale.com.
    18. "Macfarlane Burnet Medal and Lecture | Australian Academy of Science". www.science.org.au.
    19. "Research Awards". www.rmit.edu.au.
    20. "Distinguished Achievement Award - Australasian Neuroscience Society Inc". www.ans.org.au.
    21. Alan North, R.; Costa, Marcello (December 2021). "Geoffrey Burnstock. 10 May 1929—3 June 2020". Biographical Memoirs of Fellows of the Royal Society. pp. 37–58. doi:10.1098/rsbm.2021.0016.
    Max Bennett (neuroscientist)
    Portrait of Professor Max Bennett scientist.jpg
    BornFebruary 19, 1939 (1939-02-19) (age 84)
    Melbourne, Victoria, Australia
    Known forNANC synapses; calcium impulses; synapse formation & regression; synapse loss & grey matter changes; energetics of synapse function
    Academic background
    Influences Charles Scott Sherrington, Bernard Katz, Ludwig Wittgenstein