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CLIPPING

03, 04, 05, 06 e 07/03/2012
CLIPPING VIVAVOZ
Fonte: Zero Hora   Seção: Geral   Página: 21   Data: 05/03/2012
CLIPPING VIVAVOZ
Fonte: Zero Hora   Seção: Geral   Página: 27   Data: 05/03/2012
CLIPPING VIVAVOZ
Fonte: Zero Hora   Seção: Caderno   Página: 3   Data: 03/03/2012
                   Vida
CLIPPING VIVAVOZ
Fonte: Folha SP   Seção: Saúde   Página: C12   Data: 06/03/2012
CLIPPING VIVAVOZ
Fonte: Folha SP   Seção: Saúde   Página: C14   Data: 03/03/2012
CLIPPING VIVAVOZ
Fonte: Estado de   Seção: Gerais   Página: 21   Data: 07/03/2012
      Minas

                            Nem na praça
CLIPPING VIVAVOZ
Fonte: Estado de   Seção: Gerais   Página: 22   Data: 07/03/2012
      Minas

 Fumódromo tem dias contados
CLIPPING VIVAVOZ
Fonte: Guardian        Seção:                 Página:               Data: 02/03/2012


 How marijuana impairs memory

 Marijuana's effects on memory are controlled by hitherto neglected brain cells called
 astrocytes




 Marijuana is well known to impair short-term memory. Photograph: Jockmans/Rex
 Features

 My latest news story for Nature describes a new study which explains how marijuana
 causes impairments in working memory, or the ability to retain information for short
 periods of time. This is a well known side effect of marijuana, which is unwanted with
 respect to medicinal use of the drug, but until now the underlying neurobiology was
 unknown.

 The research shows that tetrahydrocanabinol (THC, the psychoactive ingredient in
 marijuana) impairs working memory by inducing a form of synaptic plasticity that
 weakens neuronal connections. This could lead to new THC-related drugs that have
 therapeutic value but do not cause this unwanted effect. More interestingly, though, the
 findings provide compelling evidence that hitherto neglected brain cells called
 astrocytes are critical for brain function and play a direct role in cognitive processes.

 There are two different types of synapitc plasticity. One of these, called long-term
 potentiation, strengthens the connections between neurons so that neurotransmission
 – the process by which signals pass from one nerve cell to another – is more effective.
 Long-term potentiation is widely believed to underly learning and memory. The other
 form, called long-term depression, has the opposite effect – it makes connections
 weaker by reducing the efficacy of neurotransmission.

 The basic principles of neurotransmission are well understood. Nervous impulses travel
 along the nerve fibre until they reach the nerve terminal. The signals cannot cross
 synapses – the tiny junctions between neurons – so they are converted into a chemical
signal. At the terminal, neurotransmitter molecules are stored in spherical structures
called vesicles, and the arrival of a nervous impulse causes these to fuse with the
terminal membrane and release their contents into the synapse. The transmitter
molecules then diffuse across the synapse and bind to receptors on the membrane of
the neighbouring cell, causing it to generate its own nervous impulses.

This process can be enhanced or diminished in a number of ways. The number of
vesicles that fuse with the terminal membrane, or the frequency with which this
happens, can both be increased, so that more transmitter molecules are released into
the synapse. Conversely, the number or frequency of these fusion events can be
decreased, so that fewer molecules are released. All of these processes are referred to
as presynaptic, because they take place in the cell that transmits the signal.

There are also postsynaptic mechanisms for altering the efficacy of transmission, which
occur at the other side of the synapse in the cell that receives the signal. The effects of
neurotransmission are determined by the receptors which bind the transmitter
molecules, so the strength of the signal can be modulated by altering the number of
receptors in the membrane of the cell on the other side of the synapse.

Receptor molecules are stored in pools located close to the membrane, and can be
shuttled back and forth between these pools and the membrane. Thus, receptors can
be inserted into the membrane by the same fusion process which causes
neurotransmitter release. They can also be removed by a reversal of the process, in
which pieces of membrane are pulled into the cell.

Long-term potentiation and memory formation are critically dependent on two types of
receptor for the neurotransmitter glutamate, called NMDA and AMPA receptors. The
new research shows that THC impairs working memory by inducing the removal of
AMPA receptors from the membranes of neurons in the hippocampus, a structure
known to be crucial for memory formation.

Shuttling of AMPA receptors into and out of nerve cell membranes is well known to
underly long-term potentiation and depression, but the new study shows, for the first
time, that removal of AMPA receptors from nerve cell membranes is controlled by
astrocytes. They express a cannabinoid receptor which, when activated by THC, sends
a signal to neurons that initiates the process.

Astrocytes are one of several types of glial cell found in the brain. The term glia means
glue in Greek, and reflects the long-standing view that these cells do little more than
support, nourish and protect neurons.

In recent years, however, it has become increasingly clear that astrocytes are far more
important than previously thought. We now know, for example, that they can send
signals not only to each other but also to neurons. They can also regulate
neurotransmission by clasping synapses with finger-like projections called endfeet.
They even build blood vessel scaffolds that guide the migration of newborn neurons

All of this suggests that astrocytes make a significant contribution to information
processing in the brain. Ever since their discovery more than a hundred years ago,
these humble cells have stood backstage in the wonderful theatre that is the brain.
Now, though, it seems that they are in fact the real stars of the show.

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03,04,05,06,07MARCO.pdf

  • 1. CLIPPING 03, 04, 05, 06 e 07/03/2012
  • 2. CLIPPING VIVAVOZ Fonte: Zero Hora Seção: Geral Página: 21 Data: 05/03/2012
  • 3. CLIPPING VIVAVOZ Fonte: Zero Hora Seção: Geral Página: 27 Data: 05/03/2012
  • 4. CLIPPING VIVAVOZ Fonte: Zero Hora Seção: Caderno Página: 3 Data: 03/03/2012 Vida
  • 5. CLIPPING VIVAVOZ Fonte: Folha SP Seção: Saúde Página: C12 Data: 06/03/2012
  • 6. CLIPPING VIVAVOZ Fonte: Folha SP Seção: Saúde Página: C14 Data: 03/03/2012
  • 7. CLIPPING VIVAVOZ Fonte: Estado de Seção: Gerais Página: 21 Data: 07/03/2012 Minas Nem na praça
  • 8.
  • 9. CLIPPING VIVAVOZ Fonte: Estado de Seção: Gerais Página: 22 Data: 07/03/2012 Minas Fumódromo tem dias contados
  • 10.
  • 11. CLIPPING VIVAVOZ Fonte: Guardian Seção: Página: Data: 02/03/2012 How marijuana impairs memory Marijuana's effects on memory are controlled by hitherto neglected brain cells called astrocytes Marijuana is well known to impair short-term memory. Photograph: Jockmans/Rex Features My latest news story for Nature describes a new study which explains how marijuana causes impairments in working memory, or the ability to retain information for short periods of time. This is a well known side effect of marijuana, which is unwanted with respect to medicinal use of the drug, but until now the underlying neurobiology was unknown. The research shows that tetrahydrocanabinol (THC, the psychoactive ingredient in marijuana) impairs working memory by inducing a form of synaptic plasticity that weakens neuronal connections. This could lead to new THC-related drugs that have therapeutic value but do not cause this unwanted effect. More interestingly, though, the findings provide compelling evidence that hitherto neglected brain cells called astrocytes are critical for brain function and play a direct role in cognitive processes. There are two different types of synapitc plasticity. One of these, called long-term potentiation, strengthens the connections between neurons so that neurotransmission – the process by which signals pass from one nerve cell to another – is more effective. Long-term potentiation is widely believed to underly learning and memory. The other form, called long-term depression, has the opposite effect – it makes connections weaker by reducing the efficacy of neurotransmission. The basic principles of neurotransmission are well understood. Nervous impulses travel along the nerve fibre until they reach the nerve terminal. The signals cannot cross synapses – the tiny junctions between neurons – so they are converted into a chemical
  • 12. signal. At the terminal, neurotransmitter molecules are stored in spherical structures called vesicles, and the arrival of a nervous impulse causes these to fuse with the terminal membrane and release their contents into the synapse. The transmitter molecules then diffuse across the synapse and bind to receptors on the membrane of the neighbouring cell, causing it to generate its own nervous impulses. This process can be enhanced or diminished in a number of ways. The number of vesicles that fuse with the terminal membrane, or the frequency with which this happens, can both be increased, so that more transmitter molecules are released into the synapse. Conversely, the number or frequency of these fusion events can be decreased, so that fewer molecules are released. All of these processes are referred to as presynaptic, because they take place in the cell that transmits the signal. There are also postsynaptic mechanisms for altering the efficacy of transmission, which occur at the other side of the synapse in the cell that receives the signal. The effects of neurotransmission are determined by the receptors which bind the transmitter molecules, so the strength of the signal can be modulated by altering the number of receptors in the membrane of the cell on the other side of the synapse. Receptor molecules are stored in pools located close to the membrane, and can be shuttled back and forth between these pools and the membrane. Thus, receptors can be inserted into the membrane by the same fusion process which causes neurotransmitter release. They can also be removed by a reversal of the process, in which pieces of membrane are pulled into the cell. Long-term potentiation and memory formation are critically dependent on two types of receptor for the neurotransmitter glutamate, called NMDA and AMPA receptors. The new research shows that THC impairs working memory by inducing the removal of AMPA receptors from the membranes of neurons in the hippocampus, a structure known to be crucial for memory formation. Shuttling of AMPA receptors into and out of nerve cell membranes is well known to underly long-term potentiation and depression, but the new study shows, for the first time, that removal of AMPA receptors from nerve cell membranes is controlled by astrocytes. They express a cannabinoid receptor which, when activated by THC, sends a signal to neurons that initiates the process. Astrocytes are one of several types of glial cell found in the brain. The term glia means glue in Greek, and reflects the long-standing view that these cells do little more than support, nourish and protect neurons. In recent years, however, it has become increasingly clear that astrocytes are far more important than previously thought. We now know, for example, that they can send signals not only to each other but also to neurons. They can also regulate neurotransmission by clasping synapses with finger-like projections called endfeet. They even build blood vessel scaffolds that guide the migration of newborn neurons All of this suggests that astrocytes make a significant contribution to information processing in the brain. Ever since their discovery more than a hundred years ago, these humble cells have stood backstage in the wonderful theatre that is the brain. Now, though, it seems that they are in fact the real stars of the show.