Dopamine levels in the brain’s substantia nigra do normally fall with ageing. However, they have to fall to one-fifth of normal values for the symptoms and signs of parkinsonism to emerge

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The basal ganglia, through the action of dopamine, are responsible for planning and controlling automatic movements of the body, such as pointing with a finger, pulling on a sock, writing or walking. If the basal ganglia are not working properly, as in Parkinson’s disease patients, all aspects of movement are impaired, resulting in the characteristic features of the disease ﾐ slowness of movement, stiffness and effort required to move a limb and, often, tremor.

The basal ganglia, through the action of dopamine, are responsible for planning and controlling automatic movements of the body, such as pointing with a finger, pulling on a sock, writing or walking. If the basal ganglia are not working properly, as in Parkinson’s disease patients, all aspects of movement are impaired, resulting in the characteristic features of the disease ﾐ slowness of movement, stiffness and effort required to move a limb and, often, tremor.

Dopamine levels in the brain’s substantia nigra do normally fall with ageing. However, they have to fall to one-fifth of normal values for the symptoms and signs of parkinsonism to emerge.

Dopamine levels in the brain’s substantia nigra do normally fall with ageing. However, they have to fall to one-fifth of normal values for the symptoms and signs of parkinsonism to emerge.

http://www.parkinsonshealth.com/AboutPD/Section.aspx?SectionId=798d598e-2a1c-4747-ac81-cd92f475744b

http://www.parkinsonshealth.com/AboutPD/Section.aspx?SectionId=798d598e-2a1c-4747-ac81-cd92f475744b
http://www.medindia.net/animation/parkinsons_disease.asp

James Parkinson (1755-1824), while best remembered for the disease state named after him by Charcot, was a man of many talents and interests.

James Parkinson (1755-1824), while best remembered for the disease state named after him by Charcot, was a man of many talents and interests.

Publishing on chemistry, paleontology and other diverse topics, he was, early in his career, a social activist championing the rights of the disenfranchised and poor.

Publishing on chemistry, paleontology and other diverse topics, he was, early in his career, a social activist championing the rights of the disenfranchised and poor.
His efforts in this area were enough to result in his arrest and appearance before The Privy Council in London on at least one occasion.
In collaboration with his son, who was a surgeon, he also offered the first description, in the English language, of a ruptured appendix.

His small but famous publication, "Essay on the Shaking Palsy", appeared in 1817, 7 years before his death in 1824.

His small but famous publication, "Essay on the Shaking Palsy", appeared in 1817, 7 years before his death in 1824.

The clinical description of 6 patients was a remarkable masterpiece testifying to his prodigious powers of observation for most of the 6 were never actually examined by Parkinson himself; rather, they were simply observed walking on the streets of London.

The clinical description of 6 patients was a remarkable masterpiece testifying to his prodigious powers of observation for most of the 6 were never actually examined by Parkinson himself; rather, they were simply observed walking on the streets of London.

Since PD is related to a deficiency of dopamine, it would be appropriate to administer dopamine

Since PD is related to a deficiency of dopamine, it would be appropriate to administer dopamine
Problem: Dopamine does not cross BBB, since it is too polar

Arvid Carlsson (b. January 25, 1923) is a Swedish scientist who is best known for his work with the neurotransmitter dopamine and its effects in Parkinson's disease.

Arvid Carlsson (b. January 25, 1923) is a Swedish scientist who is best known for his work with the neurotransmitter dopamine and its effects in Parkinson's disease.
Carlsson won the Nobel Prize in Physiology or Medicine in 2000 along with co-recipients Eric Kandel and Paul Greengard.

In the 1950s, Carlsson demonstrated that dopamine was a neurotransmitter in the brain and not just a precursor for norepinephrine, as had been previously believed.

In the 1950s, Carlsson demonstrated that dopamine was a neurotransmitter in the brain and not just a precursor for norepinephrine, as had been previously believed.
He developed a method for measuring the amount of dopamine in brain tissues and found that dopamine levels in the basal ganglia, a brain area important for movement, were particularly high.

Carlsson then showed that giving animals the drug reserpine caused a decrease in dopamine levels and a loss of movement control. These effects were similar to the symptoms of Parkinson's disease.

Carlsson then showed that giving animals the drug reserpine caused a decrease in dopamine levels and a loss of movement control. These effects were similar to the symptoms of Parkinson's disease.
By administering to these animals L-Dopa, a precursor to dopamine, he could alleviate the symptoms. These findings led other doctors try L-Dopa with human Parkinson's patients and found it to alleviate some of the symptoms in the early stages of Parkinson's. L-Dopa is still today the cornerstone of Parkinson therapy.

If dopamine is too polar to cross the BBB, how can L-DOPA cross it?

If dopamine is too polar to cross the BBB, how can L-DOPA cross it?

L-DOPA is transported across the BBB by an amino acid transport system (same one used for tyrosine and phenylalanine)

L-DOPA is transported across the BBB by an amino acid transport system (same one used for tyrosine and phenylalanine)
Once across, L-DOPA is decarboxylated to dopamine by Dopa Decarboxylase (DDC).

In actual practice, L-DOPA is almost always coadminstered together with an inhibitor of aromatic L-amino acid decarboxylase, so it doesn’t get converted to dopamine before it crosses the BBB.

In actual practice, L-DOPA is almost always coadminstered together with an inhibitor of aromatic L-amino acid decarboxylase, so it doesn’t get converted to dopamine before it crosses the BBB.
The inhibitor commonly used is carbidopa, which does not cross the BBB itself.
The inhibitor also prevents undesirable side effects of dopamine release into the PNS, including nausea.

http://www.learningcommons.umn.edu/neuro/mod6/carb.html

http://www.learningcommons.umn.edu/neuro/mod6/carb.html

Selegiline (l-deprenyl, Eldepryl® or Anipryl® veterinary) is a drug used for the treatment of early-stage Parkinson's disease and senile dementia.

Selegiline (l-deprenyl, Eldepryl® or Anipryl® veterinary) is a drug used for the treatment of early-stage Parkinson's disease and senile dementia.
In normal clinical doses it is a selective irreversible MAO-B inhibitor.

In late stage Parkinson’s Disease, Selegiline is usually added to levodopa to prolong and enhance its effect

In late stage Parkinson’s Disease, Selegiline is usually added to levodopa to prolong and enhance its effect

Entacapone is marketed by Novartis as Comtan in the US

Entacapone is marketed by Novartis as Comtan in the US
Stalevo is a combination of Levodopa, Carbidopa, and Entacapone

Endorphins (or more correctly Endomorphines) are endogenous opioid biochemical compounds. They are peptides produced by the pituitary gland and the hypothalamus in vertebrates, and they resemble the opiates in their abilities to produce analgesia and a sense of well-being. In other words, they might work as "natural pain killers." Using drugs may increase the effects of the endorphins.

Endorphins (or more correctly Endomorphines) are endogenous opioid biochemical compounds. They are peptides produced by the pituitary gland and the hypothalamus in vertebrates, and they resemble the opiates in their abilities to produce analgesia and a sense of well-being. In other words, they might work as "natural pain killers." Using drugs may increase the effects of the endorphins.

Although the CNS contains less than 2% of the total serotonin in the body, serotonin plays a very important role in a range of brain functions. It is synthesized from the amino acid tryptophan.

Although the CNS contains less than 2% of the total serotonin in the body, serotonin plays a very important role in a range of brain functions. It is synthesized from the amino acid tryptophan.
Within the brain, serotonin is localised mainly in nerve pathways emerging from the raphe nuclei, a group of nuclei at the centre of the reticular formation in the Midbrain, pons and medulla.
These serotonergic pathways spread extensively throughout the brainstem, the cerebral cortex and the spinal cord.

In addition to mood control, serotonin has been linked with a wide variety of functions, including the regulation of sleep, pain perception, body temperature, blood pressure and hormonal activity.

In addition to mood control, serotonin has been linked with a wide variety of functions, including the regulation of sleep, pain perception, body temperature, blood pressure and hormonal activity.
Outside the brain, serotonin exerts a number of important effects, particularly involving the gastrointestinal and cardiovascular systems.

The pharmacology of 5-HT is extremely complex, with its actions being mediated by a large and diverse range of 5-HT receptors.

The pharmacology of 5-HT is extremely complex, with its actions being mediated by a large and diverse range of 5-HT receptors.
At least seven different receptor "families" are known to exist, each located in different parts of the body and triggering different responses.
As with all neurotransmitters, the effects of 5-HT on the human mood and state of mind, and its role in consciousness, are very difficult to ascertain.

Serotonergic action is terminated primarily via uptake of 5-HT from the synapse. This is through the specific monoamine transporter for 5-HT, 5-HT reuptake transporter, on the presynaptic neuron.

Serotonergic action is terminated primarily via uptake of 5-HT from the synapse. This is through the specific monoamine transporter for 5-HT, 5-HT reuptake transporter, on the presynaptic neuron.
Various agents can inhibit 5-HT reuptake including MDMA (ecstasy), cocaine, tricyclic antidepressants (TCAs) and selective serotonin reuptake inhibitors (SSRIs).
Recent research suggests that serotonin plays an important role in liver regeneration and acts as a mitogen (induces cell division) throughout the body.

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Dopamine levels in the brain’s substantia nigra do normally fall with ageing. However, they have to fall to one-fifth of normal values for the symptoms and signs of parkinsonism to emerge

Dopamine levels in the brain’s substantia nigra do normally fall with ageing. However, they have to fall to one-fifth of normal values for the symptoms and signs of parkinsonism to emerge.

Dopamine levels in the brain’s substantia nigra do normally fall with ageing. However, they have to fall to one-fifth of normal values for the symptoms and signs of parkinsonism to emerge.

http://www.parkinsonshealth.com/AboutPD/Section.aspx?SectionId=798d598e-2a1c-4747-ac81-cd92f475744b

http://www.parkinsonshealth.com/AboutPD/Section.aspx?SectionId=798d598e-2a1c-4747-ac81-cd92f475744b

http://www.medindia.net/animation/parkinsons_disease.asp

James Parkinson (1755-1824), while best remembered for the disease state named after him by Charcot, was a man of many talents and interests.

James Parkinson (1755-1824), while best remembered for the disease state named after him by Charcot, was a man of many talents and interests.

Publishing on chemistry, paleontology and other diverse topics, he was, early in his career, a social activist championing the rights of the disenfranchised and poor.

Publishing on chemistry, paleontology and other diverse topics, he was, early in his career, a social activist championing the rights of the disenfranchised and poor.

His efforts in this area were enough to result in his arrest and appearance before The Privy Council in London on at least one occasion.

In collaboration with his son, who was a surgeon, he also offered the first description, in the English language, of a ruptured appendix.

His small but famous publication, "Essay on the Shaking Palsy", appeared in 1817, 7 years before his death in 1824.

His small but famous publication, "Essay on the Shaking Palsy", appeared in 1817, 7 years before his death in 1824.

The clinical description of 6 patients was a remarkable masterpiece testifying to his prodigious powers of observation for most of the 6 were never actually examined by Parkinson himself; rather, they were simply observed walking on the streets of London.

The clinical description of 6 patients was a remarkable masterpiece testifying to his prodigious powers of observation for most of the 6 were never actually examined by Parkinson himself; rather, they were simply observed walking on the streets of London.

Since PD is related to a deficiency of dopamine, it would be appropriate to administer dopamine

Since PD is related to a deficiency of dopamine, it would be appropriate to administer dopamine

Problem: Dopamine does not cross BBB, since it is too polar

Arvid Carlsson (b. January 25, 1923) is a Swedish scientist who is best known for his work with the neurotransmitter dopamine and its effects in Parkinson's disease.

Arvid Carlsson (b. January 25, 1923) is a Swedish scientist who is best known for his work with the neurotransmitter dopamine and its effects in Parkinson's disease.

Carlsson won the Nobel Prize in Physiology or Medicine in 2000 along with co-recipients Eric Kandel and Paul Greengard.

In the 1950s, Carlsson demonstrated that dopamine was a neurotransmitter in the brain and not just a precursor for norepinephrine, as had been previously believed.

In the 1950s, Carlsson demonstrated that dopamine was a neurotransmitter in the brain and not just a precursor for norepinephrine, as had been previously believed.

He developed a method for measuring the amount of dopamine in brain tissues and found that dopamine levels in the basal ganglia, a brain area important for movement, were particularly high.

Carlsson then showed that giving animals the drug reserpine caused a decrease in dopamine levels and a loss of movement control. These effects were similar to the symptoms of Parkinson's disease.

Carlsson then showed that giving animals the drug reserpine caused a decrease in dopamine levels and a loss of movement control. These effects were similar to the symptoms of Parkinson's disease.

If dopamine is too polar to cross the BBB, how can L-DOPA cross it?

If dopamine is too polar to cross the BBB, how can L-DOPA cross it?

L-DOPA is transported across the BBB by an amino acid transport system (same one used for tyrosine and phenylalanine)

L-DOPA is transported across the BBB by an amino acid transport system (same one used for tyrosine and phenylalanine)

Once across, L-DOPA is decarboxylated to dopamine by Dopa Decarboxylase (DDC).

In actual practice, L-DOPA is almost always coadminstered together with an inhibitor of aromatic L-amino acid decarboxylase, so it doesn’t get converted to dopamine before it crosses the BBB.

In actual practice, L-DOPA is almost always coadminstered together with an inhibitor of aromatic L-amino acid decarboxylase, so it doesn’t get converted to dopamine before it crosses the BBB.

The inhibitor commonly used is carbidopa, which does not cross the BBB itself.

The inhibitor also prevents undesirable side effects of dopamine release into the PNS, including nausea.

http://www.learningcommons.umn.edu/neuro/mod6/carb.html

http://www.learningcommons.umn.edu/neuro/mod6/carb.html

Selegiline (l-deprenyl, Eldepryl® or Anipryl® veterinary) is a drug used for the treatment of early-stage Parkinson's disease and senile dementia.

Selegiline (l-deprenyl, Eldepryl® or Anipryl® veterinary) is a drug used for the treatment of early-stage Parkinson's disease and senile dementia.

In normal clinical doses it is a selective irreversible MAO-B inhibitor.

In late stage Parkinson’s Disease, Selegiline is usually added to levodopa to prolong and enhance its effect

In late stage Parkinson’s Disease, Selegiline is usually added to levodopa to prolong and enhance its effect

Entacapone is marketed by Novartis as Comtan in the US

Entacapone is marketed by Novartis as Comtan in the US

Stalevo is a combination of Levodopa, Carbidopa, and Entacapone

Although the CNS contains less than 2% of the total serotonin in the body, serotonin plays a very important role in a range of brain functions. It is synthesized from the amino acid tryptophan.

Although the CNS contains less than 2% of the total serotonin in the body, serotonin plays a very important role in a range of brain functions. It is synthesized from the amino acid tryptophan.

Within the brain, serotonin is localised mainly in nerve pathways emerging from the raphe nuclei, a group of nuclei at the centre of the reticular formation in the Midbrain, pons and medulla.

These serotonergic pathways spread extensively throughout the brainstem, the cerebral cortex and the spinal cord.

In addition to mood control, serotonin has been linked with a wide variety of functions, including the regulation of sleep, pain perception, body temperature, blood pressure and hormonal activity.

In addition to mood control, serotonin has been linked with a wide variety of functions, including the regulation of sleep, pain perception, body temperature, blood pressure and hormonal activity.

Outside the brain, serotonin exerts a number of important effects, particularly involving the gastrointestinal and cardiovascular systems.

The pharmacology of 5-HT is extremely complex, with its actions being mediated by a large and diverse range of 5-HT receptors.

The pharmacology of 5-HT is extremely complex, with its actions being mediated by a large and diverse range of 5-HT receptors.

At least seven different receptor "families" are known to exist, each located in different parts of the body and triggering different responses.

As with all neurotransmitters, the effects of 5-HT on the human mood and state of mind, and its role in consciousness, are very difficult to ascertain.

Serotonergic action is terminated primarily via uptake of 5-HT from the synapse. This is through the specific monoamine transporter for 5-HT, 5-HT reuptake transporter, on the presynaptic neuron.

Serotonergic action is terminated primarily via uptake of 5-HT from the synapse. This is through the specific monoamine transporter for 5-HT, 5-HT reuptake transporter, on the presynaptic neuron.

Various agents can inhibit 5-HT reuptake including MDMA (ecstasy), cocaine, tricyclic antidepressants (TCAs) and selective serotonin reuptake inhibitors (SSRIs).

Recent research suggests that serotonin plays an important role in liver regeneration and acts as a mitogen (induces cell division) throughout the body.