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Novel Therapeutic Approaches to Neuroinflammation in Neurodegenerative Disorders: Aptamers as Central Nervous System Agents
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Introduction:
Neurodegenerative disorders (NDDs) like Alzheimer's, Parkinson's, and
multiple sclerosis all begin with neuroinflammation. Neuroinflammation targeting has recently
gained attention as a potential approach to treating several diseases affecting the central nervous
system. The objective of this review is to explore the potential of aptamers as innovative therapeutic
agents for targeting neuroinflammation in neurodegenerative disorders, offering a novel approach
to CNS treatment.
Methods:
The use of aptamers, which are single-stranded nucleic acids, in diagnostic and therapeutic
contexts may one day help overcome these obstacles. Myotrophic lateral sclerosis, Alzheimer's
disease, Parkinson's disease, and other neurodegenerative disorders are linked to neuroinflammation.
Important regulators of CNS inflammatory responses include microglia and astrocytes.
Results:
Neurotoxic (M1-phenotype microglia and A1-phenotype astrocytes) and neuroprotective
(M2-phenotype microglia and A2-phenotype astrocytes) activation of microglia and astrocytes, respectively,
is a diverse and complex process. There may be a lack of reflection of the diverse morphologies
of microglia and astrocytes in this binary categorisation. In addition to the complexity of
the relationships between these activated glial cells, the phenotypic distribution can vary as neurodegenerative
illnesses progress.
Discussion:
To create effective treatments for neurodegenerative illnesses, a deeper knowledge of
microglia and astrocyte functions is required. Drug efficacy, safety concerns, and pharmacokinetics
are only a few of the topics covered, along with the enormous possibilities and enormous hurdles
of employing aptamers as therapeutic agents.
Conclusion:
This review highlights aptamers as a promising genetic tool for treating neuroinflammation
and neurodegenerative diseases through targeted delivery to the central nervous system.
Bentham Science Publishers Ltd.
Title: Novel Therapeutic Approaches to Neuroinflammation in Neurodegenerative Disorders: Aptamers as Central Nervous System Agents
Description:
Introduction:
Neurodegenerative disorders (NDDs) like Alzheimer's, Parkinson's, and
multiple sclerosis all begin with neuroinflammation.
Neuroinflammation targeting has recently
gained attention as a potential approach to treating several diseases affecting the central nervous
system.
The objective of this review is to explore the potential of aptamers as innovative therapeutic
agents for targeting neuroinflammation in neurodegenerative disorders, offering a novel approach
to CNS treatment.
Methods:
The use of aptamers, which are single-stranded nucleic acids, in diagnostic and therapeutic
contexts may one day help overcome these obstacles.
Myotrophic lateral sclerosis, Alzheimer's
disease, Parkinson's disease, and other neurodegenerative disorders are linked to neuroinflammation.
Important regulators of CNS inflammatory responses include microglia and astrocytes.
Results:
Neurotoxic (M1-phenotype microglia and A1-phenotype astrocytes) and neuroprotective
(M2-phenotype microglia and A2-phenotype astrocytes) activation of microglia and astrocytes, respectively,
is a diverse and complex process.
There may be a lack of reflection of the diverse morphologies
of microglia and astrocytes in this binary categorisation.
In addition to the complexity of
the relationships between these activated glial cells, the phenotypic distribution can vary as neurodegenerative
illnesses progress.
Discussion:
To create effective treatments for neurodegenerative illnesses, a deeper knowledge of
microglia and astrocyte functions is required.
Drug efficacy, safety concerns, and pharmacokinetics
are only a few of the topics covered, along with the enormous possibilities and enormous hurdles
of employing aptamers as therapeutic agents.
Conclusion:
This review highlights aptamers as a promising genetic tool for treating neuroinflammation
and neurodegenerative diseases through targeted delivery to the central nervous system.
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