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Leptin is essential in maintaining normal vascular compliance independent of body weight

Abstract

The adipocytokine leptin centrally regulates body weight by enhancing metabolic rate and signaling satiety, but it also has wide-ranging peripheral effects. Leptin receptors are expressed on vascular smooth muscle cells and have a role in maintaining vascular tone. We investigated the vascular effects of leptin repletion or calorie restriction on leptin-deficient mice (ob/ob) and a leptin antagonist on wild-type (WT) mice. Aortic compliance was assessed by the measurement of pulse wave velocity by noninvasive Doppler; blood pressure was measured by left ventricular catheterization. We found that ob/ob mice have much stiffer aortas than WT mice and that reduction in aortic stiffness was greater in ob/ob mice treated with leptin vs calorie restriction, despite similar weight loss. Interestingly, treating WT mice with a leptin antagonist increases aortic stiffness with no change in weight. Thus, we conclude that leptin is essential for maintaining normal aortic compliance independent of body weight.

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References

  1. Friedman JM . Leptin at 14 y of age: an ongoing story. Am J Clin Nutr 2009; 89: 973S–979S.

    Article  CAS  Google Scholar 

  2. Iribarren C, Husson G, Go AS, Lo JC, Fair JM, Rubin GD et al. Plasma leptin levels and coronary artery calcification in older adults. J Clin Endocrinol Metab 2007; 92: 729–732.

    Article  CAS  Google Scholar 

  3. Mendoza-Núñez VM, Correa-Muñoz E, Garfias-Cruz EA, Sánchez-Rodriguez MA, Galván-Duarte RE, Retana-Ugalde R . Hyperleptinemia as a risk factor for high blood pressure in the elderly. Arch Pathol Lab Med 2006; 130: 170–175.

    PubMed  Google Scholar 

  4. Singhal A, Farooqi IS, Cole TJ, O’Rahilly S, Fewtrell M, Kattenhorn M et al. Influence of leptin on arterial dispensability: a novel link between obesity and cardiovascular disease? Circulation 2002; 106: 1919–1924.

    Article  CAS  Google Scholar 

  5. Martin SS, Qasim A, Reilly MP . Leptin resistance: a possible interface of inflammation and metabolism in obesity-related cardiovascular disease. J Am Coll Cardiol 2008; 52: 1201–1210.

    Article  CAS  Google Scholar 

  6. Sierra-Honigmann MR, Nath AK, Murakami C, García-Cardeña G, Papapetropoulos A, Sessa WC et al. Biological action of leptin as an angiogenic factor. Science 1998; 281: 1683–1686.

    Article  CAS  Google Scholar 

  7. Oda A, Taniguchi T, Yokoyama M . Leptin stimulates rat aortic smooth muscle cell proliferation and migration. Kobe J Med Sci 2001; 47: 141–150.

    CAS  PubMed  Google Scholar 

  8. Winters B, Mo Z, Brooks-Asplund E, Kim S, Shoukas A, Li D et al. Reduction of obesity, as induced by leptin, reverses endothelial dysfunction in obese (Lep(ob)) mice. J Appl Physiol 2000; 89: 2382–2390.

    Article  CAS  Google Scholar 

  9. Reddy AK, Jones AD, Martono C, Caro WA, Madala S, Hartley CJ . Pulsed Doppler signal processing for use in mice: design and evaluation. IEEE Trans Biomed Eng 2005; 52: 1764–1770.

    Article  Google Scholar 

  10. Pacher P, Nagayama T, Mukhopadhyay P, Batkai S, Kass DA . Measurement of cardiac function using pressure-volume conductance catheter technique in mice and rats. Nat Protoc 2008; 2: 1422–1434.

    Article  Google Scholar 

  11. Sloan C, Tuinei J, Abel ED . Myocardial fatty acid oxidation rates remain elevated in ob/ob mice despite reversal of obesity and diabetes by caloric restriction. Circulation 2007; 116: II_89.

    Google Scholar 

  12. Camara A, Sikka G, Barabam E, Benjo A, Oh YJ, Miller KL et al. Restoration of leptin improves vascular compliance and endothelial function in obese mice exposed to intermittent hypoxia. Circulation 2008; 118: S_301.

    Google Scholar 

  13. Unger RH . Hyperleptinemia: protecting the heart from lipid overload. Hypertension 2005; 45: 1031–1034.

    Article  CAS  Google Scholar 

Download references

Acknowledgements

This study was supported by NIH/NHLBI R01-HL077785 (to CPO), R01-AG021523 (to DEB) and K08-HL076220 (to LAB), and the WW Smith Charitable Trust (to LAB).

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Correspondence to L A Barouch.

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Sikka, G., Yang, R., Reid, S. et al. Leptin is essential in maintaining normal vascular compliance independent of body weight. Int J Obes 34, 203–206 (2010). https://doi.org/10.1038/ijo.2009.208

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