Anti-inflammatory effects of glucagon-like peptide-1 (GLP-1) in coronary artery disease: a comprehensive review

Alicja Skrobucha1, Patryk Pindlowski1, Natalia Krajewska1

  • 11st Department of Cardiology, Medical University of Warsaw, Warsaw, Poland.

Insights

Glucagon-like peptide-1 (GLP-1) demonstrates anti-inflammatory effects beneficial for coronary artery disease (CAD). Further research is needed to confirm its cardioprotective potential in human trials.

Area of Science:

  • Cardiovascular Research
  • Inflammation and Immunology
  • Endocrinology

Background:

  • Coronary artery disease (CAD) is a leading cause of death, primarily driven by inflammation and atherosclerotic plaque formation.
  • Glucagon-like peptide-1 (GLP-1) is a hormone with known roles in metabolism and emerging evidence suggests anti-inflammatory properties.
  • GLP-1 receptor agonism has shown potential in regulating inflammatory pathways relevant to atherosclerosis in vitro.

Purpose of the Study:

  • To comprehensively review the potential link between the anti-inflammatory effects of GLP-1 and its role in coronary artery disease (CAD).
  • To summarize preclinical and clinical evidence regarding GLP-1's impact on atherosclerosis and CAD.

Main Methods:

  • Review of existing literature on GLP-1, inflammation, atherosclerosis, and CAD.
  • Analysis of in vitro, animal, and human studies investigating GLP-1's effects on inflammatory pathways and cardiovascular parameters.

Main Results:

  • Preclinical studies establish an anti-atherogenic effect of GLP-1 mediated by its anti-inflammatory actions, independent of lipid modulation.
  • Human studies, though limited, suggest beneficial effects of GLP-1 on endothelial function and microcirculatory integrity in CAD patients.
  • GLP-1 receptor agonism influences cytokine production, lipotoxicity, and macrophage differentiation, key processes in atherosclerosis.

Conclusions:

  • Viewing atherosclerosis as an inflammatory condition highlights new therapeutic avenues for CAD.
  • GLP-1's anti-inflammatory properties present a promising strategy for CAD prevention and treatment.
  • Larger randomized controlled trials are essential to validate the cardioprotective effects of GLP-1 receptor agonists in CAD patients.

Related Concept Videos

Glucagon-like Receptor Agonists01:24

Glucagon-like Receptor Agonists

Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
249
GPCRs Regulate Adenylyl Cylase Activity01:09

GPCRs Regulate Adenylyl Cylase Activity

Some GPCRs transmit signals through adenylyl cyclase (AC), a transmembrane enzyme. AC helps synthesize second messenger cyclic adenosine monophosphate (cAMP). AC catalyzes cyclization reaction and converts ATP to cAMP by releasing a pyrophosphate. The pyrophosphate is further hydrolyzed to phosphate by the enzyme pyrophosphatase, which drives cAMP synthesis to completion. However, cAMP is rapidly degraded to 5′ AMP by the enzymes phosphodiesterase (PDE), preventing overstimulation of...
5.0K
Dipeptidyl Peptidase 4 Inhibitors01:23

Dipeptidyl Peptidase 4 Inhibitors

Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a...
117
Oral Hypoglycemic Agents: α-Glucosidase Inhibitors01:19

Oral Hypoglycemic Agents: α-Glucosidase Inhibitors

α-glucosidase inhibitors, including acarbose (Precose), miglitol (Glyset), and voglibose (Voglib) (primarily available in Asia), are drugs that control blood sugar levels by delaying the digestion of starch and disaccharides. They achieve this by inhibiting α-glucosidase enzymes in the intestine, which slow the absorption of carbohydrates in the intestine, which in turn leads to a prolonged release of the glucoregulatory hormone GLP-1 from intestinal L-cells.
Acarbose and miglitol are...
104
Hormones Regulating Blood Glucose01:16

Hormones Regulating Blood Glucose

Insulin is released by beta cells of the pancreas when blood glucose levels are high. It facilitates glucose absorption and utilization in insulin-dependent cells with insulin receptors on their plasma membranes. Insulin promotes glucose uptake by increasing the number of glucose transport proteins in the cell membrane, allowing glucose to enter the cell. As a result, glucose utilization and ATP production are enhanced.
In addition to accelerating glucose uptake and utilization, insulin has...
2.9K
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System01:26

Heart Failure Drugs: Inhibitors of Renin-Angiotensin System

The activation of the sympathetic nervous system and the renin-angiotensin-aldosterone system (RAAS) contributes to cardiac remodeling, and inhibiting the RAAS is a pharmacological target in heart failure management. As a result, neurohumoral modulation is a crucial treatment principle for managing heart failure. This approach involves using medications like ACE inhibitors (ACEIs), angiotensin receptor blockers (ARBs), β-blockers, mineralocorticoid receptor antagonists (MRAs), and neutral...
299