Marisela Morales (neuroscientist)

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Marisela Morales
Marisela Morales (2017).jpg
Morales in 2017
Alma mater Instituto Politécnico Nacional
Universidad de Guanajuato
Awards PECASE (2004)
Scientific career
FieldsNeuroscience
Institutions National Institute on Drug Abuse

Marisela Morales is a Mexican neuroscientist specializing in the neurobiology of drug addiction. She is a senior investigator at the National Institute on Drug Abuse.

Contents

Education

Morales completed a B.S. in biochemistry and microbiology at the Instituto Politécnico Nacional. She earned a M.S. and Ph.D. in biochemistry and cell biology at Universidad de Guanajuato Institute of Experimental Biology. Morales was a postdoctoral researcher at the University of Colorado Boulder under Eva Fifková and Scripps Research under Floyd E. Bloom. [1]

Alex Azar and Morales at the PECASE 2004 ceremony Marisela Morales PECASE 2004.jpg
Alex Azar and Morales at the PECASE 2004 ceremony

Career

In 2004, she won a Presidential Early Career Award for Scientists and Engineers for her research using a combination of molecular biology and high-resolution microscopy to identify and study brain neuronal networks that participate in the biology of various drugs of abuse. [2]

Morales is a senior investigator at the National Institute on Drug Abuse. She works in the neuronal networks section in the integrative neuroscience research branch. [3]

Research

Morales investigates the molecules, cells and neuronal pathways central to the neurobiology of drug addiction. She applies anatomical, cell molecular, cell biological and electrophysiological experimental approaches. Her laboratory's research focus on two issues: what is the brain circuitry through which addictive drugs have their habit-forming actions, and what are the neuroadaptations in this circuitry that accompany the transition from recreational to compulsive drug-taking? [1]

Morales investigates the neuronal properties and synaptic connectivity of the ventral tegmental area (VTA) to gain a better understanding of the interactions of the VTA with other brain structures in the processing and integration of information underlying behaviors associated with the neurobiology of drugs of addiction. Her laboratory has shown that glutamatergic neurons are also present in the VTA. Morales explores the neuronal connectivity of VTA glutamatergic neurons and their participation in animal behavior. [1] Her laboratory has found evidence indicating synaptic connectivity between the reward and the stress systems at the level of the VTA. [1]

Related Research Articles

<span class="mw-page-title-main">Neurotransmitter</span> Chemical substance that enables neurotransmission

A neurotransmitter is a signaling molecule secreted by a neuron to affect another cell across a synapse. The cell receiving the signal, or target cell, may be another neuron, but could also be a gland or muscle cell.

<span class="mw-page-title-main">Striatum</span> Nucleus in the basal ganglia of the brain

The striatum or corpus striatum is a nucleus in the subcortical basal ganglia of the forebrain. The striatum is a critical component of the motor and reward systems; receives glutamatergic and dopaminergic inputs from different sources; and serves as the primary input to the rest of the basal ganglia.

The mesolimbic pathway, sometimes referred to as the reward pathway, is a dopaminergic pathway in the brain. The pathway connects the ventral tegmental area in the midbrain to the ventral striatum of the basal ganglia in the forebrain. The ventral striatum includes the nucleus accumbens and the olfactory tubercle.

<span class="mw-page-title-main">Nucleus accumbens</span> Region of the basal forebrain

The nucleus accumbens is a region in the basal forebrain rostral to the preoptic area of the hypothalamus. The nucleus accumbens and the olfactory tubercle collectively form the ventral striatum. The ventral striatum and dorsal striatum collectively form the striatum, which is the main component of the basal ganglia. The dopaminergic neurons of the mesolimbic pathway project onto the GABAergic medium spiny neurons of the nucleus accumbens and olfactory tubercle. Each cerebral hemisphere has its own nucleus accumbens, which can be divided into two structures: the nucleus accumbens core and the nucleus accumbens shell. These substructures have different morphology and functions.

<span class="mw-page-title-main">Dopaminergic pathways</span> Projection neurons in the brain that synthesize and release dopamine

Dopaminergic pathways in the human brain are involved in both physiological and behavioral processes including movement, cognition, executive functions, reward, motivation, and neuroendocrine control. Each pathway is a set of projection neurons, consisting of individual dopaminergic neurons.

<span class="mw-page-title-main">Ventral tegmental area</span> Group of neurons on the floor of the midbrain

The ventral tegmental area (VTA), also known as the ventral tegmental area of Tsai, or simply ventral tegmentum, is a group of neurons located close to the midline on the floor of the midbrain. The VTA is the origin of the dopaminergic cell bodies of the mesocorticolimbic dopamine system and other dopamine pathways; it is widely implicated in the drug and natural reward circuitry of the brain. The VTA plays an important role in a number of processes, including reward cognition and orgasm, among others, as well as several psychiatric disorders. Neurons in the VTA project to numerous areas of the brain, ranging from the prefrontal cortex to the caudal brainstem and several regions in between.

Neuropharmacology is the study of how drugs affect function in the nervous system, and the neural mechanisms through which they influence behavior. There are two main branches of neuropharmacology: behavioral and molecular. Behavioral neuropharmacology focuses on the study of how drugs affect human behavior (neuropsychopharmacology), including the study of how drug dependence and addiction affect the human brain. Molecular neuropharmacology involves the study of neurons and their neurochemical interactions, with the overall goal of developing drugs that have beneficial effects on neurological function. Both of these fields are closely connected, since both are concerned with the interactions of neurotransmitters, neuropeptides, neurohormones, neuromodulators, enzymes, second messengers, co-transporters, ion channels, and receptor proteins in the central and peripheral nervous systems. Studying these interactions, researchers are developing drugs to treat many different neurological disorders, including pain, neurodegenerative diseases such as Parkinson's disease and Alzheimer's disease, psychological disorders, addiction, and many others.

<span class="mw-page-title-main">Neurotransmission</span> Impulse transmission between neurons

Neurotransmission is the process by which signaling molecules called neurotransmitters are released by the axon terminal of a neuron, and bind to and react with the receptors on the dendrites of another neuron a short distance away. A similar process occurs in retrograde neurotransmission, where the dendrites of the postsynaptic neuron release retrograde neurotransmitters that signal through receptors that are located on the axon terminal of the presynaptic neuron, mainly at GABAergic and glutamatergic synapses.

<span class="mw-page-title-main">Reward system</span> Group of neural structures responsible for motivation and desire

The reward system is a group of neural structures responsible for incentive salience, associative learning, and positively-valenced emotions, particularly ones involving pleasure as a core component. Reward is the attractive and motivational property of a stimulus that induces appetitive behavior, also known as approach behavior, and consummatory behavior. A rewarding stimulus has been described as "any stimulus, object, event, activity, or situation that has the potential to make us approach and consume it is by definition a reward". In operant conditioning, rewarding stimuli function as positive reinforcers; however, the converse statement also holds true: positive reinforcers are rewarding.

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.

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References

  1. 1 2 3 4 PD-icon.svg This article incorporates text from this source, which is in the public domain : "NIDA IRP - Marisela Morales, Ph.D." NIDA IRP. Retrieved 2021-09-22.
  2. PD-icon.svg This article incorporates text from this source, which is in the public domain : "Presidential Early Career Award for Scientists and Engineers (PECASE)". NIH Intramural Research Program. 2011-05-19. Retrieved 2021-09-22.
  3. PD-icon.svg This article incorporates text from this source, which is in the public domain : "Principal Investigators". NIH Intramural Research Program. Retrieved 2021-09-22.
PD-icon.svg This article incorporates public domain material from websites or documents of the National Institutes of Health.