Novel Myocardial PET/CT Receptor Imaging and Potential Therapeutic Targets

Curr Cardiol Rep. 2019 May 18;21(7):55. doi: 10.1007/s11886-019-1148-2.

Abstract

Purpose of the review: Activation of myocardial cannabinoid type 1 receptors (CB1-R) and/or angiotensin II type 1 receptors (AT1-R) likely plays an important mechanistic role in determining the left-ventricular remodeling process in systolic heart failure. We provide an overview on novel radiotracer probes and positron emission tomography (PET)/computed tomography (CT) imaging to noninvasively probe the expression of myocardial CB1-R and/or AT1-R.

Recent findings: Recent translational investigations have demonstrated the feasibility of 11C-OMAR or 11C-KR31173 and PET/CT to image and quantify myocardial CB1-R and/or AT1-R expression, respectively. There is an increasing understanding of the mechanisms of activated myocardial CB1-R and/or AT1-R to influence the left-ventricular remodeling process in systolic heart failure in different disease entities. The review summarizes contributions of PET to image myocardial CB1-R and AT1-R expression that may have the potential to serve as a target to tailor preventive medical care in the individual patient.

Keywords: Angiotensin II type 1 receptors; Angiotensin-converting enzyme; Cannabinoid type 1 receptor; Heart failure; Left-ventricular remodeling; Obesity; Positron emission tomography.

Publication types

  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Heart / diagnostic imaging*
  • Heart Failure / etiology
  • Heart Failure / metabolism
  • Humans
  • Myocardium / metabolism*
  • Positron Emission Tomography Computed Tomography / methods*
  • Radiopharmaceuticals / pharmacokinetics
  • Receptor, Angiotensin, Type 1 / metabolism*
  • Receptors, Cannabinoid / metabolism*
  • Ventricular Dysfunction, Left / complications*
  • Ventricular Dysfunction, Left / metabolism
  • Ventricular Remodeling

Substances

  • Radiopharmaceuticals
  • Receptor, Angiotensin, Type 1
  • Receptors, Cannabinoid