Authors

  • Makhbuba Zaynieva
    National University of Uzbekistan
  • Sabrina Murodillayeva
    National University of Uzbekistan
  • Sabina Izzatillayeva
    National University of Uzbekistan
  • Sherali Kuziev
    National University of Uzbekistan

DOI:

https://doi.org/10.71337/inlibrary.uz.ijms.76162

Abstract

Parkinson's disease (PD) is a progressive neurodegenerative disease of the central nervous system, manifested by movement disorders and symptoms of immobility. The relevance of the disease is determined by its prevalence, disability, and high socio-economic burden. The main pathophysiological mechanism of PD is the progressive loss of dopaminergic neurons in the substantia nigra pars compacta, which leads to dopamine deficiency in the striatum. The purpose of this thesis is to analyze the mechanisms of development of PD and modern methods of correction.

 

 

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PARKINSON'S DISEASE: DEVELOPMENT MECHANISMS AND MODERN

CORRECTION METHODS

Zaynieva Makhbuba

Master of National University of Uzbekistan

anvaroripov74@gmail.com

Murodillayeva Sabrina

Master of National University of Uzbekistan

sabrinamurodillayeva6@gmail.com

Izzatillayeva Sabina

Master of National University of Uzbekistan

izzatillayevasabina3@gmail.com

Kuziev Sherali

Associate Professor of the

National University of Uzbekistan, PhD

kuziev.sherali@gmail.com

Abstract:

Parkinson's disease (PD) is a progressive neurodegenerative disease of the central

nervous system, manifested by movement disorders and symptoms of immobility. The

relevance of the disease is determined by its prevalence, disability, and high socio-economic

burden. The main pathophysiological mechanism of PD is the progressive loss of

dopaminergic neurons in the substantia nigra pars compacta, which leads to dopamine

deficiency in the striatum. The purpose of this thesis is to analyze the mechanisms of

development of PD and modern methods of correction.

Keywords:

Parkinson's disease, rotenone

Development mechanisms

Genetic and environmental factors play an important role in the development of PD. Among

the genetic factors, mutations in genes such as SNCA, LRRK2, PARK2, PINK1, and DJ-1

are of particular importance. The proteins of these genes play an important role in the

normal functioning of neurons, in particular, in mitochondrial function, lysosomal

degradation, and synaptic transmission. Among environmental factors, exposure to

pesticides (e.g., rotenone, paraquat), heavy metals (manganese, lead), and industrial toxins

(trichloroethylene) has been found to increase the risk of developing PD. In addition, age,


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brain injuries, and certain diseases (e.g., diabetes, depression) may also contribute to the

development of PD [1, 2].

Modern correction methods

Currently, there is no cure for PD, but symptoms can be controlled and quality of life

improved. Medications play a major role in the treatment of PD. Levodopa is a precursor of

dopamine, which increases dopamine levels in the striatum and significantly improves motor

symptoms. Dopamine agonists (pramipexole, ropinirole) stimulate dopamine receptors and

have fewer side effects than levodopa. MAO-B inhibitors (selegiline, rasagiline) and COMT

inhibitors (entacapone, tolcapone) slow the breakdown of dopamine and prolong the effect

of levodopa [3].

Neurosurgical procedures, in particular deep brain stimulation (DBS), are used in cases

where medication is not effective. DBS helps control symptoms by placing electrodes in

specific areas of the brain. Pallidotomy and thalamotomy aim to reduce tremor by surgically

removing specific parts of the brain [4].

Rehabilitation plays an important role in improving the quality of life of patients with PK.

Physiotherapy helps improve motor functions, speech therapy helps correct speech disorders,

and occupational therapy helps maintain daily living skills [5].

Conclusion

PD is a complex neurodegenerative disease in which genetic and environmental factors play

a significant role. Currently, there is no cure for PD, but modern medications, neurosurgical

techniques, and rehabilitation can help control symptoms and improve quality of life. Future

research should focus on developing gene therapy, neuroprotective drugs, and early

diagnosis methods.

References

1.

Jankovic J. Parkinson's disease: clinical features and diagnosis. J Neurol Neurosurg

Psychiatry. 2008;79:368-376.

2.

Kalia LV, Lang AE. Parkinson's disease. Lancet. 2015;386:896-912.

3.

Olanow CW, Stern MB, Langston JW. Pergolide monotherapy in untreated

Parkinson's disease. Neurology. 1992;42:86-91.

4.

DeLong MR. Deep brain stimulation for Parkinson's disease: surgical anatomy and

pathophysiology. Mov Disord. 2003;18 Suppl 3:S6-13.

5.

Keus SH, Munneke M, Graziano M, et al. European Physiotherapy Guideline for

Parkinson's Disease. KNGF/ParkinsonNet. 2014.

References

Jankovic J. Parkinson's disease: clinical features and diagnosis. J Neurol Neurosurg Psychiatry. 2008;79:368-376.

Kalia LV, Lang AE. Parkinson's disease. Lancet. 2015;386:896-912.

Olanow CW, Stern MB, Langston JW. Pergolide monotherapy in untreated Parkinson's disease. Neurology. 1992;42:86-91.

DeLong MR. Deep brain stimulation for Parkinson's disease: surgical anatomy and pathophysiology. Mov Disord. 2003;18 Suppl 3:S6-13.

Keus SH, Munneke M, Graziano M, et al. European Physiotherapy Guideline for Parkinson's Disease. KNGF/ParkinsonNet. 2014.

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