Clinical Trials Directory

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UnknownNCT05105165

Regulatory Mechanism of Orphanin FQ in Patients With Chronic Ischemic Heart Failure

Correlation Between Serum Orphanin FQ and β1-AR Autoantibodies in Patients With Chronic Ischemic Heart Failure and Its Regulatory Mechanism

Status
Unknown
Phase
Study type
Observational
Enrollment
180 (estimated)
Sponsor
Second Hospital of Shanxi Medical University · Academic / Other
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

β 1 adrenergic autoantibody on cardiomyocytes β 1 adrenergic receptor increased the occurrence of malignant arrhythmia in patients with chronic heart failure, accelerated myocardial cell damage, and participated in sudden cardiac death. Our team found for the first time that endogenous orphanin enkephalin promotes arrhythmia after acute myocardial ischemia in rats, and its mechanism includes PKC pathway, regulation of action potential duration and cell membrane surface β 1 adrenoceptor internalization disorder. At the same time, N / OFQ can regulate the level of immune factors, and immune factors participate in the formation of β1-aa. This study will be verified by clinical observation and animal experiments: first, N / OFQ, IL-6 and chronic ischemic heart failure, and β 1-aa; second, relationship between IL-6 gene 572G / C polymorphism and chronic ischemic heart failure correlation of β 1-aa production; last, objective to verify whether N / OFQ is involved in the regulation of IL-6 on chronic ischemic heart failure by knocking out N/ OFQ gene in the animal model of chronic ischemic heart failure. So as to clarify the mechanism of myocardial cell and extracellular injury, and find a new target for the treatment of chronic heart failure.

Conditions

Interventions

TypeNameDescription
DIAGNOSTIC_TESTEnzyme linked immunosorbent assayDetermination of serum β 1-aa content

Timeline

Start date
2021-11-01
Primary completion
2022-11-28
Completion
2022-12-31
First posted
2021-11-03
Last updated
2021-11-03

Source: ClinicalTrials.gov record NCT05105165. Inclusion in this directory is not an endorsement.