Presentation is loading. Please wait.

Presentation is loading. Please wait.

Toxic Metabolites of Dopamine and PD MARTA MADZELAN XIAO YU WANG ZHOU (JOEY) TONG PUJA BOSE PHM142 Fall 2014 Coordinator: Dr. Jeffrey Henderson Instructor:

Similar presentations


Presentation on theme: "Toxic Metabolites of Dopamine and PD MARTA MADZELAN XIAO YU WANG ZHOU (JOEY) TONG PUJA BOSE PHM142 Fall 2014 Coordinator: Dr. Jeffrey Henderson Instructor:"— Presentation transcript:

1 Toxic Metabolites of Dopamine and PD MARTA MADZELAN XIAO YU WANG ZHOU (JOEY) TONG PUJA BOSE PHM142 Fall 2014 Coordinator: Dr. Jeffrey Henderson Instructor: Dr. David Hampson

2 What is Parkinson’s Disease? ● Progressive neurodegenerative disease of the CNS, primarily affecting voluntary, controlled movement ● It is a result of the chronic loss of dopaminergic neurons within the ventral component of the pars compacta region in the substantia nigra (midbrain) ● As the neurons die, less dopamine is produced and transported to the striatum (co-ordinates movement). ● In Canada, estimated prevalence rate is 100 to 200/100,000

3 What causes PD? ● Etiology is unknown (idiopathic) ● Genetic factors (small number of cases) o around 15% of individuals with PD have a first-degree relative who has the disease. ● Environmental factors (chronic exposure to pesticides) o correlation between exposure to pesticide use and wood preservatives. o strong negative correlation between cigarette smoking and the development of the disease.

4 Symptoms of PD Motor Symptoms ● Resting Tremor ● Rigidity ● Slowness of movement ● Postural Instability Non-motor Symptoms ● Autonomic dysfunction ● Neuropsychiatric symptoms ● Sleep disorders ● Sensory abnormalities *The symptoms of Parkinson’s fluctuate throughout the course of the disease and intensify progressively over time.

5 Diagnosis of PD ● Diagnosed through clinical assessment based on the symptoms described by the patient and a complete neurologic examination by the physician. ● Two of the four motor symptoms must be present to make the diagnosis. ● No lab test that identifies the disease, but brain scans are sometimes used to rule out disorders that could give rise to similar symptoms.

6 Who is at risk for PD? ● Most often occurs after the age of 50 and is one of the most common movement disorders of the elderly. ● Occurs about 50% more in men than women. ● Head trauma, illness, or exposure to environmental toxins such as pesticides ● A low % are at increased risk because of a family history (genetic factors) ● Parkinson’s can progress at a different rate for each person

7 Pathology of Parkinsons Death of dopaminergic neurons in the substantia nigra In particular, the pars compacta region Nigrostriatal pathway is one of the four major dopamine pathways Connects the substantia nigra to the striatum Is necessary for movement 80-90% of substantia nigra dopaminergic cells must die for symptoms to appear Presence of abnormal protein aggregates called Lewy Bodies

8 Dopamine Major neurotransmitter involved in a number of pathways Metabolism of dopamine generates reactive oxygen species Defensive mechanisms against ROS are overwhelmed in Parkinson’s Disease

9 Damage to Dopamine Cells D1 and D2 dopamine receptors signal through G-proteins to regulate transcription Both familial and environmental factors may contribute Accumulation of aggregated proteins is a key cause Mutations which increase ROS cause apoptosis and misfolding

10 Lewy Bodies are collections of misfolded protein Still unclear whether Lewy Bodies are a disease causing agent, an indirect consequence, or a protective measure to reduce harm

11 Treatments for Parkinson’s Disease Currently there is no treatment for Parkinson’s Disease Most “treatment” are meant to alleviate symptoms. General treatment philosophy is to address for the lack of dopamine inside the brain

12 Levodopa A metabolic precursor of dopamine. Able to cross blood-brain barrier, a tight junction that protect brain and spinal cord from general circulation. Molecules such as Decarboxylase inhibitor are usually used in combination with Levodopa in order to prevent peripheral decarboxylation of levodopa. (eg Levodopa/Carbidopa)

13 Levodopa One of the most common drug used to alleviate symptoms. Very effective in relieve symptoms like tremor and stiffness, but does not affect problems involve autonomic functions. Possible side effects include dizziness, agitation and anxiety.

14 Dopamine Agonist A type of molecule that directly stimulate the receptors in nerves in the brain that normally would be stimulated by dopamine. It behaves like dopamine but does not change into dopamine. General properties for these molecules are: easy to cross blood-brain barrier and have high affinity to dopamine receptors in brain such as D2 receptors. One example of Dopamine Agonist is Apomorphine.

15 Dopamine Agonist Less effective than Levodopa, but can help in reduce symptoms relate to motor function. Can be used in combination with Levodopa in order to decrease the side effects from Levodopa.

16 MAO-B inhibitors ● Enzyme (monoamine oxidase B) in the brain that breaks down several chemicals in the brain including dopamine ● MAO-B levels increase as you age ● Increased levels of MAO-B contribute to cellular degeneration by producing H 2 O 2 that are converted by iron to toxic O2 free radicals ● MAO-B inhibitors inhibit the activity of MAO-B allowing sustained dopamine levels

17 MAO-B Inhibitor Medications Selegiline and Rasagaline ● Usually given in the early stages but can also be given in conjunction with other drugs such as levodopa ● Stopping movements from getting worse ● Can also delay the time when patients need to start taking levodopa ● Should not be taken with antidepressants as it can raise blood pressure to dangerous levels

18 Surgery ● Surgery may be considered when drugs fail to control symptoms ● NOT A CURE! ● Deep brain stimulation - uses electrical impulses to stimulate a target area in the brain ● Pallidotomy - destruction a tiny area of the globus pallidus (tremor and stiffness) ● Thalamotomy - destruction of an area in the thalamus that controls some involuntary movement ● medications are still taken after surgery but at lesser quantities

19 Summary ● Parkinson’s is a progressive neurodegenerative disease of the CNS, primarily affecting voluntary, controlled movement ● It is a result of the chronic loss of dopaminergic neurons in the substantia nigra (midbrain) ● Currently, no cure is available for Parkinson’s disease, all treatment is meant to alleviate symptoms. ● Levodopa is a metabolic precursor of dopamine, it can cross the blood brain barrier, which separate brain from general circulation, and can be converted into dopamine inside the brain. ● Dopamine agonist is a type of molecule that stimulate the receptor that normally would be stimulated by dopamine. ● MAO (monoamine oxidase) is an enzyme in the brain that breaks down several chemicals in the brain including dopamine ● MAO-B inhibitors inhibit monoamine oxidase B which allows elevated dopamine to remain in the brain ● Parkinson results from death of over 80% of the dopaminergic neurons in the pars compacta region of the substantia nigra ● The Nigrostriatal pathway, which is responsible for movement, is disrupted during PD, causing severe motor impairment ● Degradation of dopamine naturally causes production of reactive oxygen species, but mutations in -PD patients may cause defensive mechanisms to malfunction causing abnormal oxidative stress in neurons ● Mutations in alpha-synuclein cause protein misfolding, which in turn causes increased ROS and toxicity ● These misfolded proteins aggregate into Lewy Bodies. The exact function of Lewy Bodies is unclear

20 References Moussa B. H. Youdim, Dale Edmondson & Keith F. Tipton. The Therapeutic Potential of Monoamine Oxidase Inhibitors. Nature Reviews Neuroscience 7, (April 2006) S.H Pervez and Peter Riederer. Oxidative Stress and Neuroprotection. Springer Science and Business Media, (2005) S.Lecht, S. Haroutiunian and P. Lazarovici. Rasagiline – a novel MAO B inhibitor in Parkinson’s diseasetherapy. Therapeutics and Clinical Risk Management, 3-7 (May 2009) Dauer, W., & Przedborski, S. (2003). Parkinson's Disease: Mechanism and Models. Neuron, 39(6), doi: /S (03) Girault, J.-A., & Greengard, P. (2004). The Neurobiology of Dopamine Signaling. JAMA Neurology, 61(5), doi: /archneur Tolleson, C. M., & Fang, J. Y. (2013). Advances in the Mechanisms of Parkinson’s Disease. Discovery Medicine, 18(098). Davie CA (2008). A review of Parkinson's disease. British. Medical. Bulletin. 86 (1): 109–27. Chaudhuri, K.R., Healy, D.G., Schapira, A. H.V. (2006). Non-motor symptoms of Parkinson’s disease: diagnosis and management, Lancet Neurol, 5, Burn, D.J. Parkinsonism. Retrieved from Parkinson Society Canada. (2003). Parkinson’s Disease: Social and Economic Impact [Data file]. Retrieved from Jankovic, J. (2008). Parkinson's disease: clinical features and diagnosis, Journal of Neurology, Neurosurgery & Psychiatry, 79, Parkinson's disease: clinical features and diagnosis Xie, S. (2009). Cell Signaling Technology (CST): Antibodies, Reagents, Proteomics, Kits and Consumables. Retrieved from Dopamine Signaling in Parkinson's Disease Pathway.: neuroscience/dopamine-signaling-in-parkinson-s- disease-pathway/pathways-park Zuo, L., & Motherwell, M. S. (2013). The impact of reactive oxygen species and genetic mitochondrial mutations in Parkinson's disease. Gene, 532(1), doi: /j.gene E-therapeutics, Canadian Pharmacists Association 2014, “Levodopa and Carbidopa”. Retrieved 2014/10/6 E-therapeutics, Canadian Pharmacists Association 2014, “Apomorphine”. Retrieved 2014/10/6 Growdon, et al (1998) “Levodopa improves motor function without impairing cognition in mild non-demented Parkinson's disease patients.” Neurology May;50(5): Neurology.


Download ppt "Toxic Metabolites of Dopamine and PD MARTA MADZELAN XIAO YU WANG ZHOU (JOEY) TONG PUJA BOSE PHM142 Fall 2014 Coordinator: Dr. Jeffrey Henderson Instructor:"

Similar presentations


Ads by Google