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Introduction <p>Metabolic and bariatric surgery (MBS) significantly improves diastolic dysfunction associated with heart failure with preserved ejection fraction (HFpEF), but the mechanism of improvement remains unknown. The purpose of this study was to explore whether sleeve gastrectomy (SG) in rodents improves diastolic dysfunction by enhancing nitric oxide (NO) signaling in a weight loss-independent manner.</p> Methods <p>Male, C57BL/6 mice were fed a high-fat diet (HFD) or a low-fat diet (LFD) for ten weeks and were grouped into HFD fed obese SG (SG, n = 8), HFD obese pair-fed (to SG food intake) sham (SHPF, n = 9), HFD ad lib-fed obese sham (SH, n = 10), and lean ad lib LFD-fed (LEAN, n = 12) groups. Three months after undergoing SG or sham surgery, cardiac function, cardiac gene expression, urine nitrates/nitrites, and mesenteric resistance arterial (MRA) NO expression were compared between groups.</p> Results <p>Postoperatively, the SH group gained the most amount of weight compared to the SHPF and SG groups (24.25 vs 11.62 vs 10.14&#xa0;g, respectively, <i>p</i> &lt; 0.001). The SG cohort demonstrated optimal post-operative diastolic isovolumetric relaxation time compared to the SHPF and SH groups (isovolumetric relaxation time = 7.05 vs 9.74 vs 11.33&#xa0;ms, <i>p</i> &lt; 0.001). SG mice had increased urinary nitrates/nitrites secretion (<i>p</i> = 0.03) and increased cyclic guanosine monophosphate (cGMP) expression in cardiac tissue (<i>p</i> = 0.02) compared to the SHPF group.</p> Conclusion <p>SG improves diastolic function independent of weight loss in a mouse model of obesity and metabolic syndrome. The mechanism of improvement is associated with increased urinary nitrate/nitrite secretion, suggesting higher systemic levels of NO, and increased cGMP-mediated signaling in cardiac tissue. The ability of SG to beneficially alter NO-mediated signaling and improve diastolic dysfunction suggests a potential future role of MBS as a treatment for HFpEF.</p>

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Improvement in diastolic dysfunction after bariatric and metabolic surgery is associated with enhanced nitric oxide activity

  • 期刊论文

  • 发表日期：

    2025年7月7日

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  • Sarah Suh,
  • Matthew Baron,
  • Zachary Bice,
  • Joy Lincoln,
  • Tammy Kindel

摘要

Introduction

Metabolic and bariatric surgery (MBS) significantly improves diastolic dysfunction associated with heart failure with preserved ejection fraction (HFpEF), but the mechanism of improvement remains unknown. The purpose of this study was to explore whether sleeve gastrectomy (SG) in rodents improves diastolic dysfunction by enhancing nitric oxide (NO) signaling in a weight loss-independent manner.

Methods

Male, C57BL/6 mice were fed a high-fat diet (HFD) or a low-fat diet (LFD) for ten weeks and were grouped into HFD fed obese SG (SG, n = 8), HFD obese pair-fed (to SG food intake) sham (SHPF, n = 9), HFD ad lib-fed obese sham (SH, n = 10), and lean ad lib LFD-fed (LEAN, n = 12) groups. Three months after undergoing SG or sham surgery, cardiac function, cardiac gene expression, urine nitrates/nitrites, and mesenteric resistance arterial (MRA) NO expression were compared between groups.

Results

Postoperatively, the SH group gained the most amount of weight compared to the SHPF and SG groups (24.25 vs 11.62 vs 10.14 g, respectively, p < 0.001). The SG cohort demonstrated optimal post-operative diastolic isovolumetric relaxation time compared to the SHPF and SH groups (isovolumetric relaxation time = 7.05 vs 9.74 vs 11.33 ms, p < 0.001). SG mice had increased urinary nitrates/nitrites secretion (p = 0.03) and increased cyclic guanosine monophosphate (cGMP) expression in cardiac tissue (p = 0.02) compared to the SHPF group.

Conclusion

SG improves diastolic function independent of weight loss in a mouse model of obesity and metabolic syndrome. The mechanism of improvement is associated with increased urinary nitrate/nitrite secretion, suggesting higher systemic levels of NO, and increased cGMP-mediated signaling in cardiac tissue. The ability of SG to beneficially alter NO-mediated signaling and improve diastolic dysfunction suggests a potential future role of MBS as a treatment for HFpEF.