Javascript must be enabled to continue!
Cardiorenal syndrome: pathophysiological mechanism, preclinical models, novel contributors and potential therapies
View through CrossRef
Objective
To review the current knowledge about the pathophysiological mechanisms, preclinical models, novel contributors and potential therapies of cardiorenal syndrome.
Data sources
The literature concerning cardiorenal syndrome in this review was collected from PubMed published in English up to January 2014.
Study selection
Original articles and critical reviews related to cardiorenal syndrome were selected and carefully analyzed.
Results
Cardiorenal syndrome is a condition characterized by kidney and heart failure where failure of one organ worsens the function of the other thus further accelerating the progressive failure of both organs. The pathophysiology of cardiorenal syndrome is not fully understood, but may be caused by a complex combination of neurohormonal system activation, endothelial dysfunction, proteinuria, oxidative stress, uremic toxins and other factors. Managing cardiorenal syndrome is still a major therapeutic challenge in clinical practice because many of the drugs used to control heart failure can worsen renal function, and vice versa. Non-dialyzable uremic toxins, such as indoxyl sulfate, causing detrimental effects on the heart and kidney as well as stimulation of inflammatory responses, may be an effective therapeutic target for cardiorenal syndrome.
Conclusions
Suitable disease models of cardiorenal syndrome are urgently needed to investigate the pathophysiology and effective therapeutic approaches to the condition. Non-dialyzable protein-bound uremic toxins that may have cardiac and renal effects may provide therapeutic benefit to cardiorenal syndrome patients.
Ovid Technologies (Wolters Kluwer Health)
Title: Cardiorenal syndrome: pathophysiological mechanism, preclinical models, novel contributors and potential therapies
Description:
Objective
To review the current knowledge about the pathophysiological mechanisms, preclinical models, novel contributors and potential therapies of cardiorenal syndrome.
Data sources
The literature concerning cardiorenal syndrome in this review was collected from PubMed published in English up to January 2014.
Study selection
Original articles and critical reviews related to cardiorenal syndrome were selected and carefully analyzed.
Results
Cardiorenal syndrome is a condition characterized by kidney and heart failure where failure of one organ worsens the function of the other thus further accelerating the progressive failure of both organs.
The pathophysiology of cardiorenal syndrome is not fully understood, but may be caused by a complex combination of neurohormonal system activation, endothelial dysfunction, proteinuria, oxidative stress, uremic toxins and other factors.
Managing cardiorenal syndrome is still a major therapeutic challenge in clinical practice because many of the drugs used to control heart failure can worsen renal function, and vice versa.
Non-dialyzable uremic toxins, such as indoxyl sulfate, causing detrimental effects on the heart and kidney as well as stimulation of inflammatory responses, may be an effective therapeutic target for cardiorenal syndrome.
Conclusions
Suitable disease models of cardiorenal syndrome are urgently needed to investigate the pathophysiology and effective therapeutic approaches to the condition.
Non-dialyzable protein-bound uremic toxins that may have cardiac and renal effects may provide therapeutic benefit to cardiorenal syndrome patients.
Related Results
MO667: Creating a New Cardiorenal Unit: 3-Year Study Results
MO667: Creating a New Cardiorenal Unit: 3-Year Study Results
Abstract
BACKGROUND AND AIMS
Cardiorenal syndrome is a clinical manifestation of the bidirectional interaction between the heart...
Differential Diagnosis of Neurogenic Thoracic Outlet Syndrome: A Review
Differential Diagnosis of Neurogenic Thoracic Outlet Syndrome: A Review
Abstract
Thoracic outlet syndrome (TOS) is a complex and often overlooked condition caused by the compression of neurovascular structures as they pass through the thoracic outlet. ...
Three in One: Systemic Lupus Erythematosus, HELLP Syndrome, and Antiphospholipid Syndrome: A Case Report and Literature Review
Three in One: Systemic Lupus Erythematosus, HELLP Syndrome, and Antiphospholipid Syndrome: A Case Report and Literature Review
Abstract
Introduction
Systemic lupus erythematosus (SLE) is a multisystem autoimmune disease commonly affecting women of reproductive age. Its overlap with HELLP syndrome (Hemolysi...
Analisis Asuhan Keperawatan Pada Pasien Chronic Kidney Disease Dengan Cardiorenal Syndrome di Ruang Intensif Care Unit
Analisis Asuhan Keperawatan Pada Pasien Chronic Kidney Disease Dengan Cardiorenal Syndrome di Ruang Intensif Care Unit
Penyakit ginjal dan jantung merupakan penyakit yang memiliki tingkat morbiditas dan mortalitas yang tinggi. Organ ginjal dan jantung memiliki faktor risiko vaskular yang sama dan s...
Higenamine Improves Cardiac and Renal Fibrosis in Rats With Cardiorenal Syndrome via ASK1 Signaling Pathway
Higenamine Improves Cardiac and Renal Fibrosis in Rats With Cardiorenal Syndrome via ASK1 Signaling Pathway
Abstract:
The pathogenesis of cardiorenal syndrome (CRS) is very complex, and currently there is no effective treatment for CRS. Higenamine (HI) has been shown to improve...
Documentary support for preclinical studies in vivo in accordance with the principles of Good Laboratory Practice
Documentary support for preclinical studies in vivo in accordance with the principles of Good Laboratory Practice
INTRODUCTION. Currently, the Eurasian Economic Union (EAEU) lacks guidelines for documenting preclinical studies. At the same time, proper registration of raw data is necessary to ...
Overview of Cardiorenal Syndrome
Overview of Cardiorenal Syndrome
Cardiorenal syndrome is a complex clinical condition affecting both the kidney and the heart. It is divided into 5 different subgroups according to various clinical features. Howev...
Down Syndrome
Down Syndrome
Abstract
Down syndrome, first described by Langdon Down in 1866, is caused by an extra copy of all or part of chromosome 21. It is the most comm...

