<i>Desmodesmus</i> Extract as a Mitochondrion-Targeted Neuroprotective Agent in Parkinson’s Disease: An In Vitro Study

Parkinson’s disease (PD) is the second most common neurodegenerative disease, and its prevalence is expected to double in the next 30 years. Currently, no effective treatment exists for Parkinson’s disease. Thus, the research has focused on discovering new natural compounds with strong neuroprotecti...

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Main Authors: Muazzez Derya-Andeden, Pinar Altin-Celik, Enver Ersoy Andeden, Hamiyet Donmez-Altuntas
Format: Article
Language:English
Published: MDPI AG 2025-03-01
Series:Current Issues in Molecular Biology
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Online Access:https://www.mdpi.com/1467-3045/47/3/174
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author Muazzez Derya-Andeden
Pinar Altin-Celik
Enver Ersoy Andeden
Hamiyet Donmez-Altuntas
author_facet Muazzez Derya-Andeden
Pinar Altin-Celik
Enver Ersoy Andeden
Hamiyet Donmez-Altuntas
author_sort Muazzez Derya-Andeden
collection DOAJ
description Parkinson’s disease (PD) is the second most common neurodegenerative disease, and its prevalence is expected to double in the next 30 years. Currently, no effective treatment exists for Parkinson’s disease. Thus, the research has focused on discovering new natural compounds with strong neuroprotective potential. This study aimed to investigate the effects of the methanol extract of <i>Desmodesmus arthrodesmiformis</i> EM13 (DaMe) on the mitochondrial damage pathway in an in vitro model of PD. The isolate of <i>Desmodesmus arthrodesmiformis</i> EM13 was first grown under appropriate culture conditions, and then the extract (DaMe) was prepared for use in the experiments. The total lipid and protein contents, fatty acid composition, and elemental content of DaMe were subsequently determined. Human SH-SY5Y neuroblastoma cells were pretreated with nontoxic concentrations of DaMe before 6-hydroxydopamine (6-OHDA) toxicity. Pretreatment with DaMe at concentrations of 100, 250, and 500 µg/mL showed a neuroprotective effect on 6-OHDA-induced SH-SY5Y neuroblastoma cells by decreasing the reactive oxygen species (ROS) production, decreasing the total oxidant status (TOS), increasing the total antioxidant capacity (TAC), increasing the mitochondrial membrane potential (ΔΨm), decreasing the oxidative DNA damage, and regulating gene expressions related to PD and apoptosis. Given the results of our study, we suggest that DaMe can be used as a natural source for producing drugs and dietary supplements intended to treat PD.
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spelling doaj-art-77e596d239304ffa89e3984c10c2b0322025-08-20T02:42:42ZengMDPI AGCurrent Issues in Molecular Biology1467-30371467-30452025-03-0147317410.3390/cimb47030174<i>Desmodesmus</i> Extract as a Mitochondrion-Targeted Neuroprotective Agent in Parkinson’s Disease: An In Vitro StudyMuazzez Derya-Andeden0Pinar Altin-Celik1Enver Ersoy Andeden2Hamiyet Donmez-Altuntas3Department of Medical Biology, Faculty of Medicine, Erciyes University, 38030 Kayseri, TürkiyeDepartment of Medical Biology, Faculty of Medicine, Erciyes University, 38030 Kayseri, TürkiyeDepartment of Molecular Biology and Genetics, Faculty of Art and Science, Hacı Bektaş Veli University, 50300 Nevşehir, TürkiyeDepartment of Medical Biology, Faculty of Medicine, Erciyes University, 38030 Kayseri, TürkiyeParkinson’s disease (PD) is the second most common neurodegenerative disease, and its prevalence is expected to double in the next 30 years. Currently, no effective treatment exists for Parkinson’s disease. Thus, the research has focused on discovering new natural compounds with strong neuroprotective potential. This study aimed to investigate the effects of the methanol extract of <i>Desmodesmus arthrodesmiformis</i> EM13 (DaMe) on the mitochondrial damage pathway in an in vitro model of PD. The isolate of <i>Desmodesmus arthrodesmiformis</i> EM13 was first grown under appropriate culture conditions, and then the extract (DaMe) was prepared for use in the experiments. The total lipid and protein contents, fatty acid composition, and elemental content of DaMe were subsequently determined. Human SH-SY5Y neuroblastoma cells were pretreated with nontoxic concentrations of DaMe before 6-hydroxydopamine (6-OHDA) toxicity. Pretreatment with DaMe at concentrations of 100, 250, and 500 µg/mL showed a neuroprotective effect on 6-OHDA-induced SH-SY5Y neuroblastoma cells by decreasing the reactive oxygen species (ROS) production, decreasing the total oxidant status (TOS), increasing the total antioxidant capacity (TAC), increasing the mitochondrial membrane potential (ΔΨm), decreasing the oxidative DNA damage, and regulating gene expressions related to PD and apoptosis. Given the results of our study, we suggest that DaMe can be used as a natural source for producing drugs and dietary supplements intended to treat PD.https://www.mdpi.com/1467-3045/47/3/174Parkinson’s diseasemicroalgaeSH-SY5Y6-OHDAmitochondrial damageoxidative stress
spellingShingle Muazzez Derya-Andeden
Pinar Altin-Celik
Enver Ersoy Andeden
Hamiyet Donmez-Altuntas
<i>Desmodesmus</i> Extract as a Mitochondrion-Targeted Neuroprotective Agent in Parkinson’s Disease: An In Vitro Study
Current Issues in Molecular Biology
Parkinson’s disease
microalgae
SH-SY5Y
6-OHDA
mitochondrial damage
oxidative stress
title <i>Desmodesmus</i> Extract as a Mitochondrion-Targeted Neuroprotective Agent in Parkinson’s Disease: An In Vitro Study
title_full <i>Desmodesmus</i> Extract as a Mitochondrion-Targeted Neuroprotective Agent in Parkinson’s Disease: An In Vitro Study
title_fullStr <i>Desmodesmus</i> Extract as a Mitochondrion-Targeted Neuroprotective Agent in Parkinson’s Disease: An In Vitro Study
title_full_unstemmed <i>Desmodesmus</i> Extract as a Mitochondrion-Targeted Neuroprotective Agent in Parkinson’s Disease: An In Vitro Study
title_short <i>Desmodesmus</i> Extract as a Mitochondrion-Targeted Neuroprotective Agent in Parkinson’s Disease: An In Vitro Study
title_sort i desmodesmus i extract as a mitochondrion targeted neuroprotective agent in parkinson s disease an in vitro study
topic Parkinson’s disease
microalgae
SH-SY5Y
6-OHDA
mitochondrial damage
oxidative stress
url https://www.mdpi.com/1467-3045/47/3/174
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