Oblique dendrite

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An oblique dendrite is a dendrite that branches from an apical dendrite that emerges from the apex of a pyramidal cell. Oblique dendrites typically branch one to two times before terminating. Dendrites are extensions of the cell body of a neuron.

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Growth and development

The growth and development of oblique dendrites in rats has been linked to the type of environment, or condition, they are placed in. This is also known as environmental enrichment. The three types of conditions used in studies are an enriched conditioned, standard condition, and impoverished condition. The enriched condition contains mazes, an exercise wheel, other rats, and toys. The standard condition generally has a wheel for voluntary exercise and other rats. The impoverished condition only contains fellow rats.

Animals placed in an enriched environment had heavier, thicker cortexes and an increase in the number of dendritic branches (including oblique dendrites) in the hippocampus than the standard or impoverished condition. [1] [2] This phenomenon is known as neuroplasticity. Furthermore, the enriched condition may show in increase in monoamine neurotransmitter release such as serotonin and noradrenaline which have been linked to synaptic plasticity and learning. [3] This is important because an increase in oblique dendrites and dendritic branching allows for increased neurotransmitter uptake. Environmental enrichment is crucial in early brain development due to increase formation of synapses, or synaptogenesis. This results in an increase in oblique dendrites and dendritic branching.

Effects on oblique dendrites from Alzheimer’s disease

The beta amyloid peptide, which may lead to the formation of amyloid plaques, has been linked to Alzheimer's disease. The peptide has been shown to block A-type voltage-gated potassium channel in pyramidal cell dendrites; the thin branches of the oblique dendrites are especially susceptible to disruption from the beta amyloid blockage of the A-type potassium channels which may lead to decline in cognitive function in the early stages of Alzheimer's disease. [4]

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Related Research Articles

Dendrite Small projection on a neuron that receive signals

Dendrites, also dendrons, are branched protoplasmic extensions of a nerve cell that propagate the electrochemical stimulation received from other neural cells to the cell body, or soma, of the neuron from which the dendrites project. Electrical stimulation is transmitted onto dendrites by upstream neurons via synapses which are located at various points throughout the dendritic tree. Dendrites play a critical role in integrating these synaptic inputs and in determining the extent to which action potentials are produced by the neuron. Dendritic arborization, also known as dendritic branching, is a multi-step biological process by which neurons form new dendritic trees and branches to create new synapses. The morphology of dendrites such as branch density and grouping patterns are highly correlated to the function of the neuron. Malformation of dendrites is also tightly correlated to impaired nervous system function. Some disorders that are associated with the malformation of dendrites are autism, depression, schizophrenia, Down syndrome and anxiety.

Neuron Electrically excitable cell that communicates via synapses

A neuron or nerve cell is an electrically excitable cell that communicates with other cells via specialized connections called synapses. It is the main component of nervous tissue in all animals except sponges and placozoa. Plants and fungi do not have nerve cells.

Dendritic spine Small protrusion on a dendrite that receives input from a single axon

A dendritic spine is a small membranous protrusion from a neuron's dendrite that typically receives input from a single axon at the synapse. Dendritic spines serve as a storage site for synaptic strength and help transmit electrical signals to the neuron's cell body. Most spines have a bulbous head, and a thin neck that connects the head of the spine to the shaft of the dendrite. The dendrites of a single neuron can contain hundreds to thousands of spines. In addition to spines providing an anatomical substrate for memory storage and synaptic transmission, they may also serve to increase the number of possible contacts between neurons. It has also been suggested that changes in the activity of neurons have a positive effect on spine morphology.

Dentate gyrus Region of the hippocampus in the brain

The dentate gyrus (DG) is part of the hippocampal formation in the temporal lobe of the brain that includes the hippocampus and the subiculum. The dentate gyrus is part of the hippocampal trisynaptic circuit and is thought to contribute to the formation of new episodic memories, the spontaneous exploration of novel environments and other functions.

Brain-derived neurotrophic factor Protein

Brain-derived neurotrophic factor (BDNF), or abrineurin, is a protein that, in humans, is encoded by the BDNF gene. BDNF is a member of the neurotrophin family of growth factors, which are related to the canonical nerve growth factor. Neurotrophic factors are found in the brain and the periphery. BDNF was first isolated from pig brain in 1982 by Yves-Alain Barde and Hans Thoenen.

Pyramidal cell

Pyramidal cells, or pyramidal neurons, are a type of multipolar neuron found in areas of the brain including the cerebral cortex, the hippocampus, and the amygdala. Pyramidal neurons are the primary excitation units of the mammalian prefrontal cortex and the corticospinal tract. Pyramidal neurons are also one of two cell types where the characteristic sign, Negri bodies, are found in post-mortem rabies infection. Pyramidal neurons were first discovered and studied by Santiago Ramón y Cajal. Since then, studies on pyramidal neurons have focused on topics ranging from neuroplasticity to cognition.

Adult neurogenesis

Adult neurogenesis is the process in which neurons are generated from neural stem cells in the adult. This process differs from prenatal neurogenesis.

Molecular neuroscience is a branch of neuroscience that observes concepts in molecular biology applied to the nervous systems of animals. The scope of this subject covers topics such as molecular neuroanatomy, mechanisms of molecular signaling in the nervous system, the effects of genetics and epigenetics on neuronal development, and the molecular basis for neuroplasticity and neurodegenerative diseases. As with molecular biology, molecular neuroscience is a relatively new field that is considerably dynamic.

An apical dendrite is a dendrite that emerges from the apex of a pyramidal cell. Apical dendrites are one of two primary categories of dendrites, and they distinguish the pyramidal cells from spiny stellate cells in the cortices. Pyramidal cells are found in the prefrontal cortex, the hippocampus, the entorhinal cortex, the olfactory cortex, and other areas. Dendrite arbors formed by apical dendrites are the means by which synaptic inputs into a cell are integrated. The apical dendrites in these regions contribute significantly to memory, learning, and sensory associations by modulating the excitatory and inhibitory signals received by the pyramidal cells.

Brian R. Christie is a Professor of Medicine and Neuroscience at The University of Victoria. He helped found the Neuroscience Graduate Program at the University of Victoria and served as its director from 2010–2017. He is a Michael Smith Senior Scholar Award winner. Christie received his PhD in 1992 from the University of Otago before doing postdoctoral work with Daniel Johnston at Baylor College of Medicine and Terrence Sejnowski at the Salk Institute for Biological Studies, and then became Assistant Professor at the University of British Columbia. Promoted to Associate Professor in 2007. Full Professor in 2013.

Subgranular zone

The subgranular zone (SGZ) is a brain region in the hippocampus where adult neurogenesis occurs. The other major site of adult neurogenesis is the subventricular zone (SVZ) in the brain.

Environmental enrichment Brain stimulation through physical and social surroundings

Environmental enrichment is the stimulation of the brain by its physical and social surroundings. Brains in richer, more stimulating environments have higher rates of synaptogenesis and more complex dendrite arbors, leading to increased brain activity. This effect takes place primarily during neurodevelopment, but also during adulthood to a lesser degree. With extra synapses there is also increased synapse activity, leading to an increased size and number of glial energy-support cells. Environmental enrichment also enhances capillary vasculation, providing the neurons and glial cells with extra energy. The neuropil expands, thickening the cortex. Research on rodent brains suggests that environmental enrichment may also lead to an increased rate of neurogenesis.

Activity-dependent plasticity is a form of functional and structural neuroplasticity that arises from the use of cognitive functions and personal experience; hence, it is the biological basis for learning and the formation of new memories. Activity-dependent plasticity is a form of neuroplasticity that arises from intrinsic or endogenous activity, as opposed to forms of neuroplasticity that arise from extrinsic or exogenous factors, such as electrical brain stimulation- or drug-induced neuroplasticity. The brain's ability to remodel itself forms the basis of the brain's capacity to retain memories, improve motor function, and enhance comprehension and speech amongst other things. It is this trait to retain and form memories that is associated with neural plasticity and therefore many of the functions individuals perform on a daily basis. This plasticity occurs as a result of changes in gene expression which are triggered by signaling cascades that are activated by various signaling molecules during increased neuronal activity.

Nonsynaptic plasticity

Nonsynaptic plasticity is a form of neuroplasticity that involves modification of ion channel function in the axon, dendrites, and cell body that results in specific changes in the integration of excitatory postsynaptic potentials and inhibitory postsynaptic potentials. Nonsynaptic plasticity is a modification of the intrinsic excitability of the neuron. It interacts with synaptic plasticity, but it is considered a separate entity from synaptic plasticity. Intrinsic modification of the electrical properties of neurons plays a role in many aspects of plasticity from homeostatic plasticity to learning and memory itself. Nonsynaptic plasticity affects synaptic integration, subthreshold propagation, spike generation, and other fundamental mechanisms of neurons at the cellular level. These individual neuronal alterations can result in changes in higher brain function, especially learning and memory. However, as an emerging field in neuroscience, much of the knowledge about nonsynaptic plasticity is uncertain and still requires further investigation to better define its role in brain function and behavior.

Mark Rosenzweig (psychologist)

Mark Richard Rosenzweig was an American research psychologist whose research on neuroplasticity in animals indicated that the adult brain remains capable of anatomical remodelling and reorganization based on life experiences, overturning the conventional wisdom that the brain reached full maturity in childhood.

Malleability of intelligence describes the processes by which intelligence can increase or decrease over time and is not static. These changes may come as a result of genetics, pharmacological factors, psychological factors, behavior, or environmental conditions. Malleable intelligence may refer to changes in cognitive skills, memory, reasoning, or muscle memory related motor skills. In general, the majority of changes in human intelligence occur at either the onset of development, during the critical period, or during old age.

Granule cell Type of neuron with a very small cell body

The name granule cell has been used for a number of different types of neuron whose only common feature is that they all have very small cell bodies. Granule cells are found within the granular layer of the cerebellum, the dentate gyrus of the hippocampus, the superficial layer of the dorsal cochlear nucleus, the olfactory bulb, and the cerebral cortex.

Compartmental modelling of dendrites deals with multi-compartment modelling of the dendrites, to make the understanding of the electrical behavior of complex dendrites easier. Basically, compartmental modelling of dendrites is a very helpful tool to develop new biological neuron models. Dendrites are very important because they occupy the most membrane area in many of the neurons and give the neuron an ability to connect to thousands of other cells. Originally the dendrites were thought to have constant conductance and current but now it has been understood that they may have active Voltage-gated ion channels, which influences the firing properties of the neuron and also the response of neuron to synaptic inputs. Many mathematical models have been developed to understand the electric behavior of the dendrites. Dendrites tend to be very branchy and complex, so the compartmental approach to understand the electrical behavior of the dendrites makes it very useful.

Addiction is a state characterized by compulsive engagement in rewarding stimuli, despite adverse consequences. The process of developing an addiction occurs through instrumental learning, which is otherwise known as operant conditioning.

Psychosocial genomics (PG) is a field of research first proposed by Ernest L. Rossi in 2002. PG examines the modulation of gene expression in response to psychological, social and cultural experiences. Independent research shows that the experience of novelty, environmental enrichment and exercise facilitates activity and experience dependent gene expression and brain plasticity as well as stem cell healing processes.

References

  1. Watson, Neil, Breedlove, Marc "The Mind's Machine: Foundations of Brain and Behavior" Sinauer Associates, 2012, Chapter 13: Memory, Learning, and Development
  2. van Praag, Henriette, Gerd Kempermann, and Fred H. Gage. "Neural consequences of environmental enrichment." Nature Reviews Neuroscience 1.3 (2000): 191-198.
  3. van Praag, Henriette, Gerd Kempermann, and Fred H. Gage. "Neural consequences of environmental enrichment." Nature Reviews Neuroscience 1.3 (2000): 191-198.
  4. Morse, Thomas M., Nicholas T. Carnevale, Pradeep G. Mutalik, Michele Migliore, and Gordon M. Shepherd. "Abnormal excitability of oblique dendrites implicated in early Alzheimer's: a computational study." National Center for Biotechnology Information. U.S. National Library of Medicine, 31 May 2010.

Dailey ME and Smith SJ, The Dynamics of Dendritic Structure in Developing Hippocampal Slices. J Neurosci 16(9), 1996 pp. 2983-2994.

Watson, Neil V., and S. Marc. Breedlove, "The Mind's Machine: Foundations of Brain and Behavior". Sunderland, MA: Sinauer Associates, 2012. N. pag. Print.

van Praag, Henriette, Gerd Kempermann, and Fred H. Gage. "Neural consequences of environmental enrichment." Nature Reviews Neuroscience 1.3 (2000): 191-198.

Morse, Thomas M., Nicholas T. Carnevale, Pradeep G. Mutalik, Michele Migliore, and Gordon M. Shepherd. "Abnormal excitability of oblique dendrites implicated in early Alzheimer's: a computational study." National Center for Biotechnology Information. U.S. National Library of Medicine, 31 May 2010.