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February 20, 2009Journal of Neurochemistry

AT1 receptor antagonists inhibited dopamine degeneration and early microglial and NADPH activation in MPTP-treated mice and primary mesencephalic cultures.

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Why the study?

Do AT1 receptor antagonists prevent dopamine degeneration and microglial activation in the MPTP model of Parkinson's disease?

Population

Primary mesencephalic cultures and mice (MPTP model of Parkinson's disease)

Design

Preclinical

Key result

AT1 receptor antagonists inhibited dopamine degeneration and early microglial and NADPH activation in MPTP-treated mice and primary mesencephalic cultures.

Authors

BJBelen JoglarJRJannette Rodríguez‐PallaresARAna I. Rodríguez‐Pérez

Discussion

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Member takes

Overview

AT1 antagonists merit exploration as neuroprotective agents in Parkinson's; leaves open translation from MPTP models to clinical use.

Structured PICO

Do AT1 receptor antagonists prevent dopamine degeneration and microglial activation in the MPTP model of Parkinson's disease?

P
Population
Primary mesencephalic cultures and mice (MPTP model of Parkinson's disease)
I
Intervention
AT1 receptor antagonists
O
Outcome
Dopamine (DA) degenerationsurrogate

The brain angiotensin system may mediate the inflammatory response in Parkinson's disease, suggesting AT1 receptor antagonists as a potential neuroprotective target.

Cite This Study

Joglar et al. (2009) studied Parkinson's disease (MPTP model). AT1 receptor antagonists was evaluated on Dopamine degeneration and microglial/NADPH activation. AT1 receptor antagonists inhibited dopamine degeneration and early microglial and NADPH activation in MPTP-treated mice and primary mesencephalic cultures.

synapsesocial.com/papers/6a7a17200b10e553598948c5https://doi.org/10.1111/j.1471-4159.2009.05999.x
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