Intraperitoneal delivery of acetate-encapsulated liposomal nanoparticles for neuroprotection of the penumbra in a rat model of ischemic stroke

Po-Wah So,1 Antigoni Ekonomou,1 Kim Galley,1 Leigh Brody,2 Meliz Sahuri-Arisoylu,2 Ivan Rattray,3 Diana Cash,1 Jimmy D Bell2 1King’s College London, Institute of Psychiatry, Psychology and Neuroscience, Department of Neuroimaging, London, UK; 2University of Westminster, Research Centre fo...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: So PW, Ekonomou A, Galley K, Brody L, Sahuri-Arisoylu M, Rattray I, Cash D, Bell JD
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2019
Materias:
Acceso en línea:https://doaj.org/article/68d9cce5613f42339b8902509499fd53
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:68d9cce5613f42339b8902509499fd53
record_format dspace
spelling oai:doaj.org-article:68d9cce5613f42339b8902509499fd532021-12-02T07:51:08ZIntraperitoneal delivery of acetate-encapsulated liposomal nanoparticles for neuroprotection of the penumbra in a rat model of ischemic stroke1178-2013https://doaj.org/article/68d9cce5613f42339b8902509499fd532019-03-01T00:00:00Zhttps://www.dovepress.com/intraperitoneal-delivery-of-acetate-encapsulated-liposomal-nanoparticl-peer-reviewed-article-IJNhttps://doaj.org/toc/1178-2013Po-Wah So,1 Antigoni Ekonomou,1 Kim Galley,1 Leigh Brody,2 Meliz Sahuri-Arisoylu,2 Ivan Rattray,3 Diana Cash,1 Jimmy D Bell2 1King’s College London, Institute of Psychiatry, Psychology and Neuroscience, Department of Neuroimaging, London, UK; 2University of Westminster, Research Centre for Optimal Health, London, UK; 3King’s College London, Institute of Psychiatry, Psychology and Neuroscience, Department of Basic and Clinical Neuroscience, London, UK Background: Ischemic stroke is a devastating condition, with metabolic derangement and persistent inflammation enhancing the initial insult of ischaemia. Recombinant tissue plasminogen remains the only effective treatment but limited as therapy must commence soon after the onset of symptoms.Purpose: We investigated whether acetate, which modulates many pathways including inflammation, may attenuate brain injury in stroke. As acetate has a short blood half-life and high amounts irritate the gastrointestinal tract, acetate was administered encapsulated in a liposomal nanoparticle (liposomal-encapsulated acetate, LITA).Methods: Transient ischemia was induced by 90 mins middle-cerebral artery occlusion (MCAO) in Sprague-Dawley rats, and LITA or control liposomes given intraperitoneally at occlusion and daily for up to two weeks post-MCAO. Magnetic resonance imaging (MRI) was used to estimate lesion volume at 24 h, 1 and 2 weeks post-MCAO and anterior lateral ventricular volume (ALVv) at 2 weeks post-MCAO. Locomotive behaviour was tested prior to the final MRI scan. After the final scan, brains were collected, and immunohistochemistry was performed. Results: Lesion volumes were decreased by ~80% from 24 h to one-week post-MCAO, in both control and LITA groups (P<0.05). However, the lesion was increased by ~50% over the subsequent 1 to 2 weeks after MCAO in the control group (from 24.1±10.0 to 58.7±28.6 mm3; P<0.05) but remained unchanged in the LITA group. ALVv were also attenuated by LITA treatment at 2 weeks post-MCAO (177.2±11.9% and 135.3±10.9% of contralateral ALVv for control and LITA groups, respectively; P<0.05). LITA-treated animals also appeared to have improved motor activity, moving with greater average velocity than control animals. Microglial immunoreactivity was ~40% lower in the LITA group compared to the control group (P<0.05), but LITA did not modulate neurogenesis, apoptosis, histone acetylation and lipid peroxidation. Conclusion: LITA appears to attenuate the harmful chronic neuroinflammation observed during brain remodeling after a focal ischemic insult. Keywords: ischemic stroke, acetate, liposomes, neuroinflammation, microglia, mid-cerebral artery occlusionSo PWEkonomou AGalley KBrody LSahuri-Arisoylu MRattray ICash DBell JDDove Medical Pressarticleischemic strokeacetateliposomesneuroinflammationmicrogliamid-cerebral artery occlusionMedicine (General)R5-920ENInternational Journal of Nanomedicine, Vol Volume 14, Pp 1979-1991 (2019)
institution DOAJ
collection DOAJ
language EN
topic ischemic stroke
acetate
liposomes
neuroinflammation
microglia
mid-cerebral artery occlusion
Medicine (General)
R5-920
spellingShingle ischemic stroke
acetate
liposomes
neuroinflammation
microglia
mid-cerebral artery occlusion
Medicine (General)
R5-920
So PW
Ekonomou A
Galley K
Brody L
Sahuri-Arisoylu M
Rattray I
Cash D
Bell JD
Intraperitoneal delivery of acetate-encapsulated liposomal nanoparticles for neuroprotection of the penumbra in a rat model of ischemic stroke
description Po-Wah So,1 Antigoni Ekonomou,1 Kim Galley,1 Leigh Brody,2 Meliz Sahuri-Arisoylu,2 Ivan Rattray,3 Diana Cash,1 Jimmy D Bell2 1King’s College London, Institute of Psychiatry, Psychology and Neuroscience, Department of Neuroimaging, London, UK; 2University of Westminster, Research Centre for Optimal Health, London, UK; 3King’s College London, Institute of Psychiatry, Psychology and Neuroscience, Department of Basic and Clinical Neuroscience, London, UK Background: Ischemic stroke is a devastating condition, with metabolic derangement and persistent inflammation enhancing the initial insult of ischaemia. Recombinant tissue plasminogen remains the only effective treatment but limited as therapy must commence soon after the onset of symptoms.Purpose: We investigated whether acetate, which modulates many pathways including inflammation, may attenuate brain injury in stroke. As acetate has a short blood half-life and high amounts irritate the gastrointestinal tract, acetate was administered encapsulated in a liposomal nanoparticle (liposomal-encapsulated acetate, LITA).Methods: Transient ischemia was induced by 90 mins middle-cerebral artery occlusion (MCAO) in Sprague-Dawley rats, and LITA or control liposomes given intraperitoneally at occlusion and daily for up to two weeks post-MCAO. Magnetic resonance imaging (MRI) was used to estimate lesion volume at 24 h, 1 and 2 weeks post-MCAO and anterior lateral ventricular volume (ALVv) at 2 weeks post-MCAO. Locomotive behaviour was tested prior to the final MRI scan. After the final scan, brains were collected, and immunohistochemistry was performed. Results: Lesion volumes were decreased by ~80% from 24 h to one-week post-MCAO, in both control and LITA groups (P<0.05). However, the lesion was increased by ~50% over the subsequent 1 to 2 weeks after MCAO in the control group (from 24.1±10.0 to 58.7±28.6 mm3; P<0.05) but remained unchanged in the LITA group. ALVv were also attenuated by LITA treatment at 2 weeks post-MCAO (177.2±11.9% and 135.3±10.9% of contralateral ALVv for control and LITA groups, respectively; P<0.05). LITA-treated animals also appeared to have improved motor activity, moving with greater average velocity than control animals. Microglial immunoreactivity was ~40% lower in the LITA group compared to the control group (P<0.05), but LITA did not modulate neurogenesis, apoptosis, histone acetylation and lipid peroxidation. Conclusion: LITA appears to attenuate the harmful chronic neuroinflammation observed during brain remodeling after a focal ischemic insult. Keywords: ischemic stroke, acetate, liposomes, neuroinflammation, microglia, mid-cerebral artery occlusion
format article
author So PW
Ekonomou A
Galley K
Brody L
Sahuri-Arisoylu M
Rattray I
Cash D
Bell JD
author_facet So PW
Ekonomou A
Galley K
Brody L
Sahuri-Arisoylu M
Rattray I
Cash D
Bell JD
author_sort So PW
title Intraperitoneal delivery of acetate-encapsulated liposomal nanoparticles for neuroprotection of the penumbra in a rat model of ischemic stroke
title_short Intraperitoneal delivery of acetate-encapsulated liposomal nanoparticles for neuroprotection of the penumbra in a rat model of ischemic stroke
title_full Intraperitoneal delivery of acetate-encapsulated liposomal nanoparticles for neuroprotection of the penumbra in a rat model of ischemic stroke
title_fullStr Intraperitoneal delivery of acetate-encapsulated liposomal nanoparticles for neuroprotection of the penumbra in a rat model of ischemic stroke
title_full_unstemmed Intraperitoneal delivery of acetate-encapsulated liposomal nanoparticles for neuroprotection of the penumbra in a rat model of ischemic stroke
title_sort intraperitoneal delivery of acetate-encapsulated liposomal nanoparticles for neuroprotection of the penumbra in a rat model of ischemic stroke
publisher Dove Medical Press
publishDate 2019
url https://doaj.org/article/68d9cce5613f42339b8902509499fd53
work_keys_str_mv AT sopw intraperitonealdeliveryofacetateencapsulatedliposomalnanoparticlesforneuroprotectionofthepenumbrainaratmodelofischemicstroke
AT ekonomoua intraperitonealdeliveryofacetateencapsulatedliposomalnanoparticlesforneuroprotectionofthepenumbrainaratmodelofischemicstroke
AT galleyk intraperitonealdeliveryofacetateencapsulatedliposomalnanoparticlesforneuroprotectionofthepenumbrainaratmodelofischemicstroke
AT brodyl intraperitonealdeliveryofacetateencapsulatedliposomalnanoparticlesforneuroprotectionofthepenumbrainaratmodelofischemicstroke
AT sahuriarisoylum intraperitonealdeliveryofacetateencapsulatedliposomalnanoparticlesforneuroprotectionofthepenumbrainaratmodelofischemicstroke
AT rattrayi intraperitonealdeliveryofacetateencapsulatedliposomalnanoparticlesforneuroprotectionofthepenumbrainaratmodelofischemicstroke
AT cashd intraperitonealdeliveryofacetateencapsulatedliposomalnanoparticlesforneuroprotectionofthepenumbrainaratmodelofischemicstroke
AT belljd intraperitonealdeliveryofacetateencapsulatedliposomalnanoparticlesforneuroprotectionofthepenumbrainaratmodelofischemicstroke
_version_ 1718399160717148160