Aggregation components (Kavitha et al., 2013). Inhibition of

Aggregationof aberrant cytoplasmic inclusion such as disaggregated proteins and damagedorganalles are the hallmarks in most of the neurodegenerative diseases,especially in PD. Consequently, these aggregations within neurons leads to cytotoxiceffects such as overproduction of ROS and oxidative stress mediated cell loss,due to autophagy dysfunctions, but the exact cause of autophagy dysfunctionmediates neurodegeneration still unclear. In this study, MTT assay showed that differentconcentration (0.5-200 nM) of rotenone treatment to SK-N-SH cells significantlyaffects cell viability compared with untreated control cells. However, we foundthat maximal inhibition (60 %) of cell viability at 100 nM of rotenone doseconcentration, which is corroborating with previous findings (Jayaraj et al., 2013; Kavitha et al.

, 2013;Tamilselvam et al., 2013). Rotenone treatment directly affectsintracellular energy and metabolism which consequently leads ROS accumulationand cell death.

Addition of phytochemicals such as mangiferin and hesperidinprotects the neuroblastoma cells against rotenone treatment induced toxicity (Kavitha et al., 2013; Tamilselvam et al., 2013).

However, obtained results from thisstudy show that GE to rotenone treatment inhibits above 50% of the cellpopulation at the concentration 60 nM for 24 h as demonstrated in Figure 1.This is consistent with the finding in other in vitro models with relevance to PD (Jayaraj et al., 2013; Kavitha et al., 2013;Tamilselvam et al., 2013).Since, oxidative stressdependent neuronal injury was proposed to be a primary causing mechanism in PD,which involved in mitochondrial dysfunction mediates rotenone induced celldeath in SK-N-SH cells (Fiskum et al., 2003; Song et al.

Best services for writing your paper according to Trustpilot

Premium Partner
From $18.00 per page
4,8 / 5
4,80
Writers Experience
4,80
Delivery
4,90
Support
4,70
Price
Recommended Service
From $13.90 per page
4,6 / 5
4,70
Writers Experience
4,70
Delivery
4,60
Support
4,60
Price
From $20.00 per page
4,5 / 5
4,80
Writers Experience
4,50
Delivery
4,40
Support
4,10
Price
* All Partners were chosen among 50+ writing services by our Customer Satisfaction Team

, 2012). The mitochondria are one of the majorprinciple sources of ATP biosynthesis through oxidative phosphorylation for thepurpose of providing energy to cellular activities. Oxidative phosphorylationfor ATP synthesis, which is consists of five electron transport chain (ETC; I-V),which composes together with different structural proteins. A reduction orinhibition of any one of ETC could lead to disrupt the balance between ATPproduction and consumption, and results reduced ATP stores and causes electronsto accumulate within respiratory chain components (Kavitha et al., 2013). Inhibition of ETC-I that leads tothe shunting of electrons through the ETC-II, which may enhances the formationof ROS upto 5-7 times more than normal production (Fiskum et al., 2003; Selvakumar et al., 2014).

Over accumulation of intracellular ROS(as demonstrated by the DCFDA assay) major culprit for neuronal loss and a keymarker of oxidative stress and leads to a rapid consumption and depletion ofendogenous scavenging antioxidants (Moon and Paek, 2015). In addition, accumulationof ROS may quickly interacts with nearest cellular components such as proteins,  lipids, carbohydrates  and  nucleic acids as well as cytoplasmic organelles that leading to  the oxidative  damage  of these  cellular compnents,disaggregated protein accumulation and the subsequent cellular dysfunction  (Szewczyk and Wojtczak, 2002). In this study,we found that treatment with rotenone decreased activities of enzymaticantioxidants such as SOD, GSH were probably due to a response towards increasedconcentration of ROS and lipid peroxidation by TBARS as shown in Table 1.Moreover, GSH depletion, the first indicator of oxidative stress during PDprogression, indicating a concomitant increases of ROS accumulation (Sherer et al., 2003; Kavitha et al., 2013).

It was reported that abnormalproduction of ROS and NO could inhibit the cell growth and induce cell death inSK-N-SH cells (Zhao and Li, 2002; Ezoulin et al., 2008). Our current results also agreementwith previous findings, that GE appears to prevented rotenone induced celldeath by reduced ROS and NO generation, TBARS via enhanced activity of ECT-1and neutralized the endogenous antioxidant by enhancing the activities of SODand GSH in experimental group, which might be due to ROS scavenging property ofGE (Tiwari and Kakkar, 2009).

Similarly, the SN of PD brains hasa reduced level of the antioxidant enzymes suchas catalase, SOD and GPx (Sian et al., 1994a) and antioxidantmoleculessuch as GSH (Sian et al., 1994b), suggesting the presence of asustained burden of oxidative stress that overhelmed the antioxidant capacity (Liu and Ames, 2005; Liu et al., 2009).

Collectively, rotenone modelrecapitulates most of the mechanisms thought to be important in PD pathogenesis(Betarbet et al., 2002). Furthermore,rotenone promotes cell death by inducing apoptosis morphological changes such aschromatin condensation and distended mitochondria. Cells pre-treated with GEprevent the cell death by reverse of those process.

Previously it was reportedthat rotenone induces apoptotic cell death through chromatin condensation and disruptsmitochondrial structure in neuronal cells, when cells pretreated with baicaleinand naringin prevents the apoptotic morphological dependent cell death, ourresults concurrence with previous findings (Watabe and Nakaki, 2004; Kim et al., 2009; Song etal., 2012; Shangguan et al., 2017).Treatment with rotenonereduces autophagy clearance in the neuronal cells. Chu et al, (Chu et al.

, 2013) reported that rotenone treatmentrupture the mitochondrial transmembrane potential with mitophagy recognitionprotein and reduces intracellular mitophagy in neuronal cells and it is leadsto mitophagy dysfunction (Chu et al., 2013; Hou et al., 2015; Moors et al.,2017). In this study, we found thatrotenone treatment significantly reduces the mitophagy vesicle engulfment andincreased accumulation of oxidatively damaged mitochondrial (called distendedmitochondrial structure) populationsin SK-N SH cells, due to mitochondrialtransmembrane potential depolarization. Addition of GE significantly reversesthe mitophagy vesicle engulfment and decreased the accumulation of oxidativelydamaged mitochondrial in SK-N-SH cells, which indicate that GE acceleratemitophagy clearance.  Aggregation of ?-synuclein(14 kDa consists 140 amino acids, a pre-synaptic protein localized in various partsin the brain) a key marker for dopaminergic cell death in PD (Moors et al.

, 2017). Treatment of rotenone increases theaggregation of ?-Synuclein protein via oxidative stress in neuronal cells,which is decreased by centella asiaticaextract (McMurray, 2001; Berrocal et al., 2014). In the present study, we found thatGE treatment to rotenone significantly reduces ?-Synuclein expression ascompared with rotenone only treated cells, which concurrence with previousfindings (McMurray, 2001; Berrocal et al.

, 2014).ER stress arises when increasesthe misfolded protein accumulation in the cytoplasmic region due to increasedrates of synthesis and accumulation supsequently activates the UPR. The UPRconsist three branches that govern translational control and chaperone proteinexpression, PERK, IRE-1?, and ATF6 (Velculescu et al., 1995; Ron and Walter, 2007; Walterand Ron, 2011; Back and Kaufman, 2012).

Upon sensing the presence andaccumulations of unfolded or misfolded proteins, IRE1? undergoes dimerizationand trans-autophosphorylation, leads to activating its endoribonucleaseactivity. IRE1? then mediates the excision of a 26-nucleotide intron from X-boxbinding protein 1 (XBP1), resulting in a translational frameshift and formationof a potent transcriptional activator(Jiang et al., 2016)thereby activating the transcriptionof ER stress target genes.PERK is also a type I ERtransmembrane kinase. Similar to IRE1?, when activated by ER stress, PERKoligomerizes, autophosphorylates and then directly phosphorylates ? subunit ofeukaryotic initiation factor 2 (eIF2?) (Harding et al., 1999). Phosphorylated eIF2? preventsformation of ribosomal initiation complexes leading to global mRNAtranslational attenuation.

This reduction in ER workload protects cells from ERstress-mediated death. Meanwhile some mRNAs require eIF2? phosphorylation fortranslation such as the mRNA encoding ATF4. ATF4 is a b-ZIP transcriptionfactor that regulates several UPR target genes including those involved in ERstress mediated cell death such as CHOP (Harding et al., 2000).

A third regulator of ER stresssignaling is the type II ER transmembrane transcription factor, ATF6?. It wasextensively studied in the context of ER Stress. Upon ER stress conditions,ATF6? translocate to the nucleus to activate UPR genes involved in proteinfolding, processing, and degradation (Yoshida et al., 2000).

When activated, the signal transduction pathwaysinitiated by PERK, IRE1? and ATF6? induce a characteristic set of genesencoding ER chaperones and nuclear transcription factors that ultimately leadeither to reduction of ER stress or to death (Mori, 2003). Therefore, ER stress may play a prosurvival orproapoptotic role and severe ER stress triggers neuronal cell death(Vilatoba et al., 2005;Wang et al., 2008).Inthe current study, we found that the specifc mechanism of the cell activity ofthe rotenone treated cells, the ER stress (UPR pathway) associated proteins,including PERK, IRE-1? and ATF6? levels were significantly increased inrotenone treated cells, suggesting the presence of increased ER stress in thePD model (Han and Holtzman,2000; Chen et al., 2008; Han et al., 2014a; Han et al.

, 2014b; Jiang et al.,2016). And also increased levels of elf 2?, ATF4, CHOP and XBP1(Wu et al., 2013; Chen et al., 2008; Jiang et al., 2016) were observed inrotenone treated SK-N-SH cells. Pretreatment of GE observed protectiveeffect in rotenone treatment by down-regulating the ER stress offeredprotection against rotenone cytotoxicity.

Taken together, the results suggestthat by reducing the ER stress contribute a protection againstrotenone cytotoxicity.Autophagymediates lysosomal degradation of long-lived cytoplasmic proteins, initiatedunder the conditions of differentiation, stress such as oxidative stress, ERstress and protein aggregate accumulation (Yorimitsu et al., 2006; Mizushima, 2007; Sarkar etal., 2007a; Sarkar et al., 2007c). It was reported that autophagy playa crucial role in a number of neurological diseases especially in PD(Cherra and Chu, 2008; Yue et al.

, 2008). The strategy of upregulating oraccelerating autophagy to treat neurodegenerative diseases has been tested invarious cell and animal models and shown to decrease protein aggregation,maintain the cytoplasmic homeostasis leads to prevent the cell death (Sarkar et al., 2007c; Pan et al., 2009). Our study focused on the ER stressdependentactivationof autophagy during rotenone induced oxidative stressconditioncan prevent thecell loss in SK-NSH cells by GE treatment.Autophagyhas revealed that the regulatory molecules that control autophagy are varied, dependson the intracellular homeostasis including AMPKand mTOR (Meijer and Codogno, 2006). Theserine/threonine kinase mTOR, a central controller of cell growth andnegatively regulates autophagy.

mTOR kinase regulates autophagy through ATGproteins, resulting in interference with the formation of autophagosomes(Levine and Yuan, 2005). The data fromthe present study encourages the concept that GE induces a pathway of autophagythrough the downregulation of AMPK and mTOR expression in SK-N-SH cells.TheLC3-I and LC3-II proteins are critical markers for autophagy, was produced byautophagy cascade.

LC3-I exists in cytosolic form and LC3-II in membrane boundform. The ratio of conversion from LC3-I to LC3-II is closely correlated withthe extent of autophagosome formation (Kabeya et al., 2000). In addition, the autophagic proteinp62/SQSTM1 is selectively incorporated into autophagosome through directbinding to LC3 and efficiently degraded by autophagy. The level of p62inversely correlates with autophagic activity (Bjorkoy et al., 2006). Our hypothesisthat autophagy is induced during ER stress is supported by activated theautophagosome formation, which was shown in examinations of LC3-I, LC3-II.Therefore,the AMPK and mTOR dependent or ?independent mechanism may participate inpathway regulation of LC3-associated autophagosome formation in dopaminergicneurons, under normal and pathogenic conditions.

x

Hi!
I'm Dora!

Would you like to get a custom essay? How about receiving a customized one?

Click here