Trojan Horse Delivery of 4,4′‐Dimethoxychalcone for Parkinsonian Neuroprotection
Abstract Parkinson's disease (PD) is characterized by the progressive deterioration of dopamine (DA) neurons, and therapeutic endeavors are aimed at preventing DA loss. However, lack of effective brain delivery approaches limits this strategy. In this study, a “Trojan horse” system is used for...
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doaj-6be119206097450bace9d5af7bdb89dd2021-05-05T07:56:42ZengWileyAdvanced Science2198-38442021-05-0189n/an/a10.1002/advs.202004555Trojan Horse Delivery of 4,4′‐Dimethoxychalcone for Parkinsonian NeuroprotectionWenlong Zhang0Huaqing Chen1Liuyan Ding2Junwei Gong3Mengran Zhang4Wenyuan Guo5Pingyi Xu6Shiying Li7Yunlong Zhang8Department of Neurology The First Affiliated Hospital of Guangzhou Medical University Guangzhou 510120 ChinaKey Laboratory of Molecular Target & Clinical Pharmacology and the State Key Laboratory of Respiratory Disease School of Pharmaceutical Sciences & The Fifth Affiliated Hospital Guangzhou Medical University Guangzhou 511436 ChinaDepartment of Neurology The First Affiliated Hospital of Guangzhou Medical University Guangzhou 510120 ChinaKey Laboratory of Neurological Function and Health School of Basic Medical Sciences Guangzhou Medical University Guangzhou 511436 ChinaKey Laboratory of Neurological Function and Health School of Basic Medical Sciences Guangzhou Medical University Guangzhou 511436 ChinaDepartment of Neurology The First Affiliated Hospital of Guangzhou Medical University Guangzhou 510120 ChinaDepartment of Neurology The First Affiliated Hospital of Guangzhou Medical University Guangzhou 510120 ChinaKey Laboratory of Molecular Target & Clinical Pharmacology and the State Key Laboratory of Respiratory Disease School of Pharmaceutical Sciences & The Fifth Affiliated Hospital Guangzhou Medical University Guangzhou 511436 ChinaKey Laboratory of Neurological Function and Health School of Basic Medical Sciences Guangzhou Medical University Guangzhou 511436 ChinaAbstract Parkinson's disease (PD) is characterized by the progressive deterioration of dopamine (DA) neurons, and therapeutic endeavors are aimed at preventing DA loss. However, lack of effective brain delivery approaches limits this strategy. In this study, a “Trojan horse” system is used for substantia nigra‐targeted delivery of a blood brain barrier‐penetrating peptide (RVG29) conjugated to the surface of nanoparticles loaded with the natural autophagy inducer 4,4′‐dimethoxychalcone (DMC) (designated as RVG‐nDMC). Here, the neuroprotective effects of DMC are demonstrated in PD. Specifically, RVG‐nDMC penetrates the blood brain barrier with enhanced brain‐targeted delivery efficiency and is internalized by DA neurons and microglia. In vivo studies demonstrate that RVG‐nDMC ameliorates motor deficits and nigral DA neuron death in PD mice without causing overt adverse effects in the brain or other major organs. Moreover, RVG‐nDMC reverses tyrosine hydroxylase ubiquitination and degradation, alleviates oxidative stress in DA neurons, and exerts antiinflammatory effects in microglia. The “Trojan horse” strategy for targeted delivery of DMC thus provides a potentially powerful and clinically feasible approach for PD intervention.https://doi.org/10.1002/advs.202004555blood brain barrierbrain targeted deliveryDMCneuroinflammationoxidative stressTH ubiquitination |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Wenlong Zhang Huaqing Chen Liuyan Ding Junwei Gong Mengran Zhang Wenyuan Guo Pingyi Xu Shiying Li Yunlong Zhang |
spellingShingle |
Wenlong Zhang Huaqing Chen Liuyan Ding Junwei Gong Mengran Zhang Wenyuan Guo Pingyi Xu Shiying Li Yunlong Zhang Trojan Horse Delivery of 4,4′‐Dimethoxychalcone for Parkinsonian Neuroprotection Advanced Science blood brain barrier brain targeted delivery DMC neuroinflammation oxidative stress TH ubiquitination |
author_facet |
Wenlong Zhang Huaqing Chen Liuyan Ding Junwei Gong Mengran Zhang Wenyuan Guo Pingyi Xu Shiying Li Yunlong Zhang |
author_sort |
Wenlong Zhang |
title |
Trojan Horse Delivery of 4,4′‐Dimethoxychalcone for Parkinsonian Neuroprotection |
title_short |
Trojan Horse Delivery of 4,4′‐Dimethoxychalcone for Parkinsonian Neuroprotection |
title_full |
Trojan Horse Delivery of 4,4′‐Dimethoxychalcone for Parkinsonian Neuroprotection |
title_fullStr |
Trojan Horse Delivery of 4,4′‐Dimethoxychalcone for Parkinsonian Neuroprotection |
title_full_unstemmed |
Trojan Horse Delivery of 4,4′‐Dimethoxychalcone for Parkinsonian Neuroprotection |
title_sort |
trojan horse delivery of 4,4′‐dimethoxychalcone for parkinsonian neuroprotection |
publisher |
Wiley |
series |
Advanced Science |
issn |
2198-3844 |
publishDate |
2021-05-01 |
description |
Abstract Parkinson's disease (PD) is characterized by the progressive deterioration of dopamine (DA) neurons, and therapeutic endeavors are aimed at preventing DA loss. However, lack of effective brain delivery approaches limits this strategy. In this study, a “Trojan horse” system is used for substantia nigra‐targeted delivery of a blood brain barrier‐penetrating peptide (RVG29) conjugated to the surface of nanoparticles loaded with the natural autophagy inducer 4,4′‐dimethoxychalcone (DMC) (designated as RVG‐nDMC). Here, the neuroprotective effects of DMC are demonstrated in PD. Specifically, RVG‐nDMC penetrates the blood brain barrier with enhanced brain‐targeted delivery efficiency and is internalized by DA neurons and microglia. In vivo studies demonstrate that RVG‐nDMC ameliorates motor deficits and nigral DA neuron death in PD mice without causing overt adverse effects in the brain or other major organs. Moreover, RVG‐nDMC reverses tyrosine hydroxylase ubiquitination and degradation, alleviates oxidative stress in DA neurons, and exerts antiinflammatory effects in microglia. The “Trojan horse” strategy for targeted delivery of DMC thus provides a potentially powerful and clinically feasible approach for PD intervention. |
topic |
blood brain barrier brain targeted delivery DMC neuroinflammation oxidative stress TH ubiquitination |
url |
https://doi.org/10.1002/advs.202004555 |
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