Cargando…

Novel Liposomal Rolipram Formulation for Clinical Application to Reduce Emesis

INTRODUCTION: The phosphodiesterase 4 (PDE4) inhibitor, rolipram, has beneficial effects on tissue inflammation, injury and fibrosis, including in the liver. Since rolipram elicits significant CNS side-effects in humans (ie, nausea and emesis), our group developed a fusogenic lipid vesicle (FLV) dru...

Descripción completa

Detalles Bibliográficos
Autores principales: Gobejishvili, Leila, Rodriguez, Walter E, Bauer, Philip, Wang, Yali, Soni, Chirag, Lydic, Todd, Barve, Shirish, McClain, Craig, Maldonado, Claudio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078351/
https://www.ncbi.nlm.nih.gov/pubmed/35535222
http://dx.doi.org/10.2147/DDDT.S355796
_version_ 1784702311513194496
author Gobejishvili, Leila
Rodriguez, Walter E
Bauer, Philip
Wang, Yali
Soni, Chirag
Lydic, Todd
Barve, Shirish
McClain, Craig
Maldonado, Claudio
author_facet Gobejishvili, Leila
Rodriguez, Walter E
Bauer, Philip
Wang, Yali
Soni, Chirag
Lydic, Todd
Barve, Shirish
McClain, Craig
Maldonado, Claudio
author_sort Gobejishvili, Leila
collection PubMed
description INTRODUCTION: The phosphodiesterase 4 (PDE4) inhibitor, rolipram, has beneficial effects on tissue inflammation, injury and fibrosis, including in the liver. Since rolipram elicits significant CNS side-effects in humans (ie, nausea and emesis), our group developed a fusogenic lipid vesicle (FLV) drug delivery system that targets the liver to avoid adverse events. We evaluated whether this novel liposomal rolipram formulation reduces emesis. METHODS: C57Bl/6J male mice were used to compare the effect of three doses of free and FLV-delivered (FLVs-Rol) rolipram in a behavioral correlate model of rolipram-induced emesis. Tissue rolipram and rolipram metabolite levels were measured using LC-MS/MS. The effect of FLVs-Rol on brain and liver PDE4 activities was evaluated. RESULTS: Low and moderate doses of free rolipram significantly reduced anesthesia duration, while the same doses of FLVs-Rol had no effect. However, the onset and duration of adverse effects (shortening of anesthesia period) elicited by a high dose of rolipram was not ameliorated by FLVs-Rol. Post-mortem analysis of brain and liver tissues demonstrated that FLVs affected the rate of rolipram uptake by liver and brain. Lastly, administration of a moderate dose of FLVs-Rol attenuated endotoxin induced PDE4 activity in the liver with negligible effect on the brain. DISCUSSION: The findings that the low and moderate doses of FLVs-Rol did not shorten the anesthesia duration time suggest that FLV delivery prevented critical levels of drug from crossing the blood-brain barrier (BBB) to elicit CNS side-effects. However, the inability of high dose FLVs-Rol to prevent CNS side-effects indicates that there was sufficient unencapsulated rolipram to cross the BBB and shorten anesthesia duration. Notably, a moderate dose of FLVs-Rol was able to decrease PDE4 activity in the liver without affecting the brain. Taken together, FLVs-Rol has a strong potential for clinical application for the treatment of liver disease without side effects.
format Online
Article
Text
id pubmed-9078351
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher Dove
record_format MEDLINE/PubMed
spelling pubmed-90783512022-05-08 Novel Liposomal Rolipram Formulation for Clinical Application to Reduce Emesis Gobejishvili, Leila Rodriguez, Walter E Bauer, Philip Wang, Yali Soni, Chirag Lydic, Todd Barve, Shirish McClain, Craig Maldonado, Claudio Drug Des Devel Ther Original Research INTRODUCTION: The phosphodiesterase 4 (PDE4) inhibitor, rolipram, has beneficial effects on tissue inflammation, injury and fibrosis, including in the liver. Since rolipram elicits significant CNS side-effects in humans (ie, nausea and emesis), our group developed a fusogenic lipid vesicle (FLV) drug delivery system that targets the liver to avoid adverse events. We evaluated whether this novel liposomal rolipram formulation reduces emesis. METHODS: C57Bl/6J male mice were used to compare the effect of three doses of free and FLV-delivered (FLVs-Rol) rolipram in a behavioral correlate model of rolipram-induced emesis. Tissue rolipram and rolipram metabolite levels were measured using LC-MS/MS. The effect of FLVs-Rol on brain and liver PDE4 activities was evaluated. RESULTS: Low and moderate doses of free rolipram significantly reduced anesthesia duration, while the same doses of FLVs-Rol had no effect. However, the onset and duration of adverse effects (shortening of anesthesia period) elicited by a high dose of rolipram was not ameliorated by FLVs-Rol. Post-mortem analysis of brain and liver tissues demonstrated that FLVs affected the rate of rolipram uptake by liver and brain. Lastly, administration of a moderate dose of FLVs-Rol attenuated endotoxin induced PDE4 activity in the liver with negligible effect on the brain. DISCUSSION: The findings that the low and moderate doses of FLVs-Rol did not shorten the anesthesia duration time suggest that FLV delivery prevented critical levels of drug from crossing the blood-brain barrier (BBB) to elicit CNS side-effects. However, the inability of high dose FLVs-Rol to prevent CNS side-effects indicates that there was sufficient unencapsulated rolipram to cross the BBB and shorten anesthesia duration. Notably, a moderate dose of FLVs-Rol was able to decrease PDE4 activity in the liver without affecting the brain. Taken together, FLVs-Rol has a strong potential for clinical application for the treatment of liver disease without side effects. Dove 2022-05-03 /pmc/articles/PMC9078351/ /pubmed/35535222 http://dx.doi.org/10.2147/DDDT.S355796 Text en © 2022 Gobejishvili et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php).
spellingShingle Original Research
Gobejishvili, Leila
Rodriguez, Walter E
Bauer, Philip
Wang, Yali
Soni, Chirag
Lydic, Todd
Barve, Shirish
McClain, Craig
Maldonado, Claudio
Novel Liposomal Rolipram Formulation for Clinical Application to Reduce Emesis
title Novel Liposomal Rolipram Formulation for Clinical Application to Reduce Emesis
title_full Novel Liposomal Rolipram Formulation for Clinical Application to Reduce Emesis
title_fullStr Novel Liposomal Rolipram Formulation for Clinical Application to Reduce Emesis
title_full_unstemmed Novel Liposomal Rolipram Formulation for Clinical Application to Reduce Emesis
title_short Novel Liposomal Rolipram Formulation for Clinical Application to Reduce Emesis
title_sort novel liposomal rolipram formulation for clinical application to reduce emesis
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9078351/
https://www.ncbi.nlm.nih.gov/pubmed/35535222
http://dx.doi.org/10.2147/DDDT.S355796
work_keys_str_mv AT gobejishvilileila novelliposomalrolipramformulationforclinicalapplicationtoreduceemesis
AT rodriguezwaltere novelliposomalrolipramformulationforclinicalapplicationtoreduceemesis
AT bauerphilip novelliposomalrolipramformulationforclinicalapplicationtoreduceemesis
AT wangyali novelliposomalrolipramformulationforclinicalapplicationtoreduceemesis
AT sonichirag novelliposomalrolipramformulationforclinicalapplicationtoreduceemesis
AT lydictodd novelliposomalrolipramformulationforclinicalapplicationtoreduceemesis
AT barveshirish novelliposomalrolipramformulationforclinicalapplicationtoreduceemesis
AT mcclaincraig novelliposomalrolipramformulationforclinicalapplicationtoreduceemesis
AT maldonadoclaudio novelliposomalrolipramformulationforclinicalapplicationtoreduceemesis