TY - JOUR
T1 - From Antipsychotic to Neuroprotective
T2 - Computational Repurposing of Fluspirilene as a Potential PDE5 Inhibitor for Alzheimer's Disease
AU - Bhattacharya, Kunal
AU - Bhattacharjee, Atanu
AU - Chakraborty, Manodeep
AU - Das, Dibyajyoti
AU - Paudel, Keshav Raj
N1 - Publisher Copyright:
© 2025 Wiley Periodicals LLC.
PY - 2025/1/15
Y1 - 2025/1/15
N2 - Phosphodiesterase 5 (PDE5) inhibitors have shown great potential in treating Alzheimer's disease by improving memory and cognitive function. In this study, we evaluated fluspirilene, a drug commonly used to treat schizophrenia, as a potential PDE5 inhibitor using computational methods. Molecular docking revealed that fluspirilene binds strongly to PDE5, supported by hydrophobic and aromatic interactions. Molecular dynamics simulations confirmed that the fluspirilene–PDE5 complex is stable and maintains its structural integrity over time. Binding energy calculations further highlighted favorable interactions, indicating that the drug forms a strong and stable bond with PDE5. Additional analyses, including studies of protein dynamics and energy landscape mapping, revealed how the drug interacts dynamically with PDE5, adapting to different conformations and maintaining stability. These findings suggest that fluspirilene may modulate PDE5 activity, potentially offering therapeutic benefits for Alzheimer's disease. This study provides strong evidence for repurposing fluspirilene as a treatment for Alzheimer's and lays the foundation for further experimental and clinical investigations.
AB - Phosphodiesterase 5 (PDE5) inhibitors have shown great potential in treating Alzheimer's disease by improving memory and cognitive function. In this study, we evaluated fluspirilene, a drug commonly used to treat schizophrenia, as a potential PDE5 inhibitor using computational methods. Molecular docking revealed that fluspirilene binds strongly to PDE5, supported by hydrophobic and aromatic interactions. Molecular dynamics simulations confirmed that the fluspirilene–PDE5 complex is stable and maintains its structural integrity over time. Binding energy calculations further highlighted favorable interactions, indicating that the drug forms a strong and stable bond with PDE5. Additional analyses, including studies of protein dynamics and energy landscape mapping, revealed how the drug interacts dynamically with PDE5, adapting to different conformations and maintaining stability. These findings suggest that fluspirilene may modulate PDE5 activity, potentially offering therapeutic benefits for Alzheimer's disease. This study provides strong evidence for repurposing fluspirilene as a treatment for Alzheimer's and lays the foundation for further experimental and clinical investigations.
KW - Alzheimer's
KW - fluspirilene
KW - molecular docking
KW - molecular dynamics simulations
KW - phosphodiesterase 5 (PDE5) inhibitor
UR - http://www.scopus.com/inward/record.url?scp=85214983220&partnerID=8YFLogxK
U2 - 10.1002/jcc.70029
DO - 10.1002/jcc.70029
M3 - Article
C2 - 39797567
AN - SCOPUS:85214983220
SN - 0192-8651
VL - 46
JO - Journal of Computational Chemistry
JF - Journal of Computational Chemistry
IS - 2
M1 - e70029
ER -