Protective Role of Sarpogrelate in Combination with Bromocriptine and Cabergoline for Treatment of Diabetes in Alloxan-induced Diabetic Rats

ABSTRACT: Background: Although dopamine D2 receptor agonists, bromocriptine and cabergoline, are notable medications in the treatment of Parkinsonism, hyperprolactinemia, and hyperglycemia, there is an identified relationship between the utilization of D2-like R agonists and the progress of myocard...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: Mohammed Fouad Shalaby, MD, Hekma A. Abd El Latif, PhD, Mohamed El Yamani, PhD, May Ahmed Galal, PhD, Sherifa Kamal, PhD, Ikhlas Sindi, PhD
Formato: article
Lenguaje:EN
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://doaj.org/article/4071e837d64440c69aa406399cbef68a
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:4071e837d64440c69aa406399cbef68a
record_format dspace
spelling oai:doaj.org-article:4071e837d64440c69aa406399cbef68a2021-11-04T04:25:42ZProtective Role of Sarpogrelate in Combination with Bromocriptine and Cabergoline for Treatment of Diabetes in Alloxan-induced Diabetic Rats0011-393X10.1016/j.curtheres.2021.100647https://doaj.org/article/4071e837d64440c69aa406399cbef68a2021-01-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S0011393X21000254https://doaj.org/toc/0011-393XABSTRACT: Background: Although dopamine D2 receptor agonists, bromocriptine and cabergoline, are notable medications in the treatment of Parkinsonism, hyperprolactinemia, and hyperglycemia, there is an identified relationship between the utilization of D2-like R agonists and the progress of myocardial injury, especially in the early phase of therapy. Objective: This investigation aimed to examine the potential activity of sarpogrelate (a 5-hydroxytryptamine 2A [5-HT2A] receptor blocker) in reducing myocardial injury prompted by extended haul utilization of D2 receptor agonists in a model of diabetic rats. Methods: In the in vivo studies, both bromocriptine and cabergoline were managed independently and combined with sarpogrelate for about a month in diabetic nephropathy rats. Blood glucose level and other myocardial biochemical parameters were estimated. The probable mechanism for insulin secretagogue action was evaluated through in vitro isolated islets study. Sodium/potassium-adenosine triphosphatase activity was assayed in an isolated microsomal fraction of the renal cortex. Isolated perfused rat hearts were treated with different doses of dopamine before and after being subjected to the tested drugs, dose response of heart rate, and heart contractility were recorded. Results: Bromocriptine and cabergoline created a significant reduction in blood glucose level without any action on insulin secretagogues. Bromocriptine prevented the loss of sodium/potassium-adenosine triphosphatase activity in the cortex of an ischemic kidney. Treatment of bromocriptine or cabergoline with sarpogrelate altogether decreased the levels of the elevated myocardial biomarkers in serum. Administration of different doses of dopamine in presence of bromocriptine or capergoline resulted in significantly rising in the heart rate percentage comparing to dopamine alone. A mix of bromocriptine or cabergoline with sarpogrelate diminished both heart rate and contractility, respectively. Conclusions: The examination demonstrated that the combined use of sarpogrelate with bromocriptine or cabergoline decreased the potential adverse effects of these 2 drugs on myocardial tissues.Mohammed Fouad Shalaby, MDHekma A. Abd El Latif, PhDMohamed El Yamani, PhDMay Ahmed Galal, PhDSherifa Kamal, PhDIkhlas Sindi, PhDElsevierarticleCardiovascularDiabetic nephropathyDopamine receptorsMyocardial injurySarpogrelateTherapeutics. PharmacologyRM1-950ENCurrent Therapeutic Research, Vol 95, Iss , Pp 100647- (2021)
institution DOAJ
collection DOAJ
language EN
topic Cardiovascular
Diabetic nephropathy
Dopamine receptors
Myocardial injury
Sarpogrelate
Therapeutics. Pharmacology
RM1-950
spellingShingle Cardiovascular
Diabetic nephropathy
Dopamine receptors
Myocardial injury
Sarpogrelate
Therapeutics. Pharmacology
RM1-950
Mohammed Fouad Shalaby, MD
Hekma A. Abd El Latif, PhD
Mohamed El Yamani, PhD
May Ahmed Galal, PhD
Sherifa Kamal, PhD
Ikhlas Sindi, PhD
Protective Role of Sarpogrelate in Combination with Bromocriptine and Cabergoline for Treatment of Diabetes in Alloxan-induced Diabetic Rats
description ABSTRACT: Background: Although dopamine D2 receptor agonists, bromocriptine and cabergoline, are notable medications in the treatment of Parkinsonism, hyperprolactinemia, and hyperglycemia, there is an identified relationship between the utilization of D2-like R agonists and the progress of myocardial injury, especially in the early phase of therapy. Objective: This investigation aimed to examine the potential activity of sarpogrelate (a 5-hydroxytryptamine 2A [5-HT2A] receptor blocker) in reducing myocardial injury prompted by extended haul utilization of D2 receptor agonists in a model of diabetic rats. Methods: In the in vivo studies, both bromocriptine and cabergoline were managed independently and combined with sarpogrelate for about a month in diabetic nephropathy rats. Blood glucose level and other myocardial biochemical parameters were estimated. The probable mechanism for insulin secretagogue action was evaluated through in vitro isolated islets study. Sodium/potassium-adenosine triphosphatase activity was assayed in an isolated microsomal fraction of the renal cortex. Isolated perfused rat hearts were treated with different doses of dopamine before and after being subjected to the tested drugs, dose response of heart rate, and heart contractility were recorded. Results: Bromocriptine and cabergoline created a significant reduction in blood glucose level without any action on insulin secretagogues. Bromocriptine prevented the loss of sodium/potassium-adenosine triphosphatase activity in the cortex of an ischemic kidney. Treatment of bromocriptine or cabergoline with sarpogrelate altogether decreased the levels of the elevated myocardial biomarkers in serum. Administration of different doses of dopamine in presence of bromocriptine or capergoline resulted in significantly rising in the heart rate percentage comparing to dopamine alone. A mix of bromocriptine or cabergoline with sarpogrelate diminished both heart rate and contractility, respectively. Conclusions: The examination demonstrated that the combined use of sarpogrelate with bromocriptine or cabergoline decreased the potential adverse effects of these 2 drugs on myocardial tissues.
format article
author Mohammed Fouad Shalaby, MD
Hekma A. Abd El Latif, PhD
Mohamed El Yamani, PhD
May Ahmed Galal, PhD
Sherifa Kamal, PhD
Ikhlas Sindi, PhD
author_facet Mohammed Fouad Shalaby, MD
Hekma A. Abd El Latif, PhD
Mohamed El Yamani, PhD
May Ahmed Galal, PhD
Sherifa Kamal, PhD
Ikhlas Sindi, PhD
author_sort Mohammed Fouad Shalaby, MD
title Protective Role of Sarpogrelate in Combination with Bromocriptine and Cabergoline for Treatment of Diabetes in Alloxan-induced Diabetic Rats
title_short Protective Role of Sarpogrelate in Combination with Bromocriptine and Cabergoline for Treatment of Diabetes in Alloxan-induced Diabetic Rats
title_full Protective Role of Sarpogrelate in Combination with Bromocriptine and Cabergoline for Treatment of Diabetes in Alloxan-induced Diabetic Rats
title_fullStr Protective Role of Sarpogrelate in Combination with Bromocriptine and Cabergoline for Treatment of Diabetes in Alloxan-induced Diabetic Rats
title_full_unstemmed Protective Role of Sarpogrelate in Combination with Bromocriptine and Cabergoline for Treatment of Diabetes in Alloxan-induced Diabetic Rats
title_sort protective role of sarpogrelate in combination with bromocriptine and cabergoline for treatment of diabetes in alloxan-induced diabetic rats
publisher Elsevier
publishDate 2021
url https://doaj.org/article/4071e837d64440c69aa406399cbef68a
work_keys_str_mv AT mohammedfouadshalabymd protectiveroleofsarpogrelateincombinationwithbromocriptineandcabergolinefortreatmentofdiabetesinalloxaninduceddiabeticrats
AT hekmaaabdellatifphd protectiveroleofsarpogrelateincombinationwithbromocriptineandcabergolinefortreatmentofdiabetesinalloxaninduceddiabeticrats
AT mohamedelyamaniphd protectiveroleofsarpogrelateincombinationwithbromocriptineandcabergolinefortreatmentofdiabetesinalloxaninduceddiabeticrats
AT mayahmedgalalphd protectiveroleofsarpogrelateincombinationwithbromocriptineandcabergolinefortreatmentofdiabetesinalloxaninduceddiabeticrats
AT sherifakamalphd protectiveroleofsarpogrelateincombinationwithbromocriptineandcabergolinefortreatmentofdiabetesinalloxaninduceddiabeticrats
AT ikhlassindiphd protectiveroleofsarpogrelateincombinationwithbromocriptineandcabergolinefortreatmentofdiabetesinalloxaninduceddiabeticrats
_version_ 1718445324635209728