Table 1.
Current treatments of Parkinson’s disease.
| Group of treatment | Name of medicine | Pharmaceutical names | Mechanism of action | Drawbacks | Ref. |
|---|---|---|---|---|---|
| increase or substitute for dopamine | Carbidopa-levodopaa. | Lodosyn-levodopa | Levodopa converted to dopamine, carbidopa protect levodopa breakdown | Lightheadedness, nausea, dyskinesia | (Kell et al., 2017; Haddad et al., 2018; Lau et al., 2018) |
| Duopa therapya. | Duopa | Delivers the medicine in the gel, reduces motion fluctuations and movement disorders | The tube fall out, and infections, blockage in the tube | (Chaudhuri et al., 2016; LeWitt, 2016) | |
| Dopamine agonistsa. | Requip, Mirapex, Neupro | Similar effects as dopamine | Hallucinations, sleepiness, and compulsive behaviors | (Pahwa and Lyons, 2009; Kulisevsky and Pagonabarraga, 2010; Yu and Fernandez, 2017) | |
| Apomorphine | Intermittent subcutaneous injections treat the motor symptoms of PD | Hallucinations, sleepiness, and compulsive behaviors | (Patel et al, 2017; Antonini and Nitu, 2018) | ||
| MAO B inhibitorsa. | rasagiline, safinamide, selegiline, | Prevent the breakdown of brain dopamine | Nausea, insomnia, | (Dezsi and Vecsei, 2017; Binde et al., 2018; Szökő et al., 2018) | |
| COMT inhibitorsb | Comtan, Tasmar | Block the enzyme that breaks down dopamine; | Risk of serious liver damage, diarrhea, dyskinesia | (Schlesinger and Korczyn, 2016; Katsaiti and Nixon, 2018; Silva et al., 2020) | |
| Anticholinergb | Cogentin, trihexyphenid-yl | Used as monotherapy or combination regimen, they work better on tremors | Impaired memory, hallucinations, dry mouth, and impaired urination. | (Nishtala et al., 2016; Mishima et al., 2018; Morrow et al., 2018; Hong et al., 2019) | |
| Amantadineb | Amantadine | short-term relief of mild symptoms, control involuntary movements | Ankle swelling, skin purple mottling, or hallucinations | (Wolf et al., 2010; Kim et al., 2018) | |
| Creatineb | Creatine | Energy compound that exerts neuroprotective effects | Weight gain, impairment of renal function | (Xiao et al., 2014; Duarte-Silva et al., 2018; Marques and Wyse, 2019) | |
| Surgical procedures | Deep brain stimulationb | DBS | Send electrical pulses to the patient’s brain and reduces the symptoms of PD | Infection, brain hemorrhage or stroke. | (Follett et al., 2010; Lee et al., 2018) |
| Gene therapyc | Gene therapy | GAD, GABA | Alter local neurotransmitters or neurotrophic factors in the basal | Clinical results have been less encouraging | (Bartus et al., 2014) |
| Immunotherapyc | Immunotherapy | α-syn immunotherapies | Using antibodies against misfolded α-synuclein | Induction of Th17 cell-mediated inflammatory autoimmunity, | (George and Brundin, 2015) |
| Cell transplantationc | Embryonic stem cells | Fetal mesencephalic tissue, stem cell | Introducing new dopamine cells into the brain of PD | Unacceptable graft-induced dyskinesia | (Normile, 2018) |
Standard therapeutic agents.
Alternative therapeutic agents.
Therapeutical agents under investigation.