Introduction
Gut microbiota (GM) contains 100 trillion bacteria and some viruses, fungi, archaea. These microbes are 10 times greater than the number of cells present in the human body. GM contains 3 million genes which is 150 times more than the human genome. 1/3rd of the GM is similar in most people, while 2/3rd is specific for each individual. A study revealed that microbial fingerprint is unique for an individual and distinguishes him from others. 1 50-60% of the GM cannot be cultured as they have host-to-host transmission. 2, 3 Parkinson’s disease (PD) is the most common second neurodegenerative disorder which affects 1-2 people per 1000 population in the world. 4 PD affects about 7-10 million people in the world, 5 this number may double by 2030 due to aging of the people. 6 A study says that Asians are less affected than the western people and their genetic causes of PD are distinct. 7 China is the leading country with a greater number of PD patients. In 2005, it is 48% which may reach 57% by 2030 [Figure 1].
Parkinson’s disease
Parkinson's disease (PD) is a neurodegenerative disorder which causes muscular rigidity, akinesia, tremor, difficulty in walking and slowness of movement. Other symptoms include depression, dementia and dysfunction of ANS, CNS and ENS. There is a dopaminergic loss in substantia nigra pars compacta (SNpc) and it also causes α-synucleinopathy. 9, 10 80% of PD patients suffer from constipation. 11 The incidences of PD are probably higher in people between the ages 60-64 and lower at the age of 35-39 [Figure 2]
Gut microbiota and Parkinson’s disease:
GM contains one trillion microbes, among which bacteria is the dominant species in the GI tract. Bacteria contain mainly 4 phyla: Bacteroidetes, Firmicutes, Actinobacteria and Proteobacteria. 12 Helicobacter pylori is the extensively studied microbe in association with PD. H. pylori inhibits the absorption of Levodopa (drug to manage PD) and causes motor impairments. 13 PD is also associated with SIBO (Small Intestinal Bacterial Growth), excessive bacterial growth in the small intestine and it causes motor impairments. 14, 15 PD patients fecal sample analysis shows higher level of Enterobacteriaceae, which causes postural instability, 16 and lower levels of Prevotellaceae family of Bacteria, they are commensals which produce mucin and neuroactive SCFAs (propionate, acetate and butyrate). Decreased Prevotellaceae level in turn reduces the mucin synthesis, increases intestinal permeability and in the development of α-synucleinopathy. Lower prevotellaceae is also associated with increase in Lactobacillaceae, which in turn reduces the level of ghrelin (gut hormone), which is involved in nigrostriatal dopamine activity. 17 Another study reports that fecal sample of PD patient’s showincreased levels of proteobacteria of the genus Ralstonia and reduced level of bacteria of genera Roseburia, Blautia and Copococcus. But no change in the Bifido bacteria level. 18
Etiology of Parkinson’s disease:
The etiology of PD still remains unclear. It is mainly characterized by α-synucleinopathy (deposition of insoluble polymers of α-synuclein in the neuronal body and forms Lewy bodies). These Lewy bodies cause neurodegeneration and neuronal death. 20, 21 PD is associated with depauperation of dopaminergic neurons in the substantia nigra pars compacta (SNc), which causes dopamine deficiency. 22, 23, 24 Decrease in the dopamine in the basal ganglia causes motor symptoms like bradykinesia, rigidity and tremor [.Figure 3]. The non-motor symptoms include gastrointestinal dysfunction, sleep disturbances, neuropsychiatric disorders (depression, apathy, cognitive impairment, and psychosis), sensory alterations (pain, olfactory impairment). 25 Dopamine modulators are administered to manage PD, even though it has serious side effects, limited benefit and may not be effective in the later stages of PD. 24, 25, 26 PD causes constipation which is associated with neurodegeneration of ENS, 27 α-synuclein accumulation with increased oxidative stress, local inflammation and intestinal permeability. 28, 29
Gastrointestinal dysfunction in Parkinson’s disease:
According to Edwards et al31 PD patients have GI dysfunctions like abnormal salivation, constipation, dysphagia, nausea and defecatory dysfunction. Hypersalivation in PD patients is due to decreased swallowing frequency and it is symptomatic in 50% of PD patients. 32 Oropharyngeal dysfunction occurs in the oesophageal body or in the oesophageal sphincter among 60-70% of PD patients.28, 29, 30 Aspiration pneumonia occurs due to dysphagia in 15-55% of PD patients. 32, 33, 34 Impaired gastric emptying is the important characteristic of PD patients with symptoms like early satiety, bloating, abdominal discomfort and nausea. 35 Amplitude of stomach contractions has also been reduced in PD patients. 36 Delayed gastric emptying causes impaired absorption of L-dopa and increases motor fluctuations. 37 Small bowel dysmotility may be due to SIBO (small Intestinal Bacterial Overgrowth), which is increased in PD patients. 38 Constipation may be an early manifestation for PD patients. 39, 40, 41, 42, 43, 44 Colon transit time may be increased even in PD patients with asymptomatic constipation. 45 and its severity causes megacolon. 46 Incomplete evacuation and excessive straining are the symptoms of defecatory dysfunction. 47, 48
Microbiome-Gut-Brain Axis and Toll-Like Receptors in Parkinson’s Disease
Toll-like-receptors (TLR) ligands are produced by the gut microbiota; under certain conditions it can exert pro-inflammatory effects. 50 Under physiological conditions, gut has a high tolerance to TLR ligands, where as in altered gut microbiota activate TLRs which trigger downstream signalling pathways creates inflammation and oxidative stress in gut and brain in the PD patients. TLR2 and TLR4 are two major TLRs evidenced in PD patients. 50 They can trigger neurotoxicity upon their activation; in contrast they can clear misfolded α-synuclein, being neuroprotective. 51
Altered gut microbiota and inflammatory cytokine responses in patients with Parkinson’s disease
Altered GM, induces abnormal production of inflammatory cytokines, which causes neuroinflammation in PD patients. 52 Inflammatory cytokines like IL-1β, IL-8 and TNF-α in the serum causes neurotoxicity, disruption of blood brain barrier and increases microglia-mediated inflammation. 53, 54 IL-6 is the major cytokine elevated in PD patients compared to controls. SIL-2-R and TNF- α are also associated with severe symptoms of PD. It may be noted that non-motor symptoms like fatigue and depression are generated via inflammatory mechanisms. 55
Structural changes of gut microbiota in Parkinson’s disease
To analyse the structural changes, putative cellulose degrading bacteria like Ruminococcus, Blautia and Faecalibacterium and putative pathobionts like Proteus, Enterococcus, Escherichia-Shigella, Streptococcus were measured in healthy controls and PD patients. 56 The putative cellulose degraders were decreased, whereas putative pathobionts were increased, which in turn decreases the production of SCFAs (Short Chain Fatty Acids) and increase the production of neurotoxins and endotoxins. These changes in the gut microbiota are associated with PD pathology. 56
Short chain fatty acids (SCFAs and gut microbiota in Parkinson's disease
SCFAs like butyrate, propionate and acetate are significantly lower in PD patients than the healthy controls of same age. 57 whereas valerate, isovalerate and iso-butyrate concentration remains same with control and the PD patients. These SCFAs can cross the brain and regulate the microglial activation. 58 SCFAs can cause motor dysfunctions in PD patients. 59
Conclusion
GM is a potential modulator of brain and behaviour. It can directly or indirectly modify our brain neurochemistry. There is a variation in the GM in PD patients, which can be used as a biomarker to analyse PD pathogenesis. There is still a need to achieve the proper inter-relationship between GM and PD. There is no proper treatment to cure the PD patients, even though Levodopa is an anti-parkinsonian medicine, it has its own limitations. Further study is required to manage the gut microbiota and Parkinson’s disease.