Abstract

A two-way connection between obesity and lymphatic dysfunction has now been established. Clinical studies have demonstrated that obesity significantly increases the risk for developing secondary lymphedema. Using animal-models, obesity and metabolic syndrome have been linked to different aspects of lymphatic structural abnormalities and lymphatic dysfunction, including impaired contractility, impaired flow-mediated responses, impaired fluid transport, as well as increased permeability, and abnormal dendritic cell migration among others. Dysfunction of lymphatic valves is a main form of lymphatic dysfunction, known to result in severe edematous phenotypes; however, the extent of lymphatic valve deficiency in secondary lymphedema, including obesity-induced lymphedema, remains unknown. Therefore, the aims of the present study were 1) to determine whether western diet-induced obesity results in lymphatic valve dysfunction, and 2) to determine whether lymphatic valve dysfunction in western diet-induced obesity results from the diet itself, or as a consequence of the metabolic alterations induced by the diet. First, we quantitatively assessed and compared valve function in isolated popliteal and mesenteric collecting lymphatic vessels from control and western diet-induced obese C57BL/6J (WT) mice. Feeding a western diet for 14 weeks induced obesity and elevated plasma glucose and cholesterol levels when compared to controls. The function of lymphatic valves in popliteal lymphatics was not affected by diet-induced obesity; however, significant back-leak of pressure was observed in mesenteric lymphatic valves. Dysfunctional, leaky valves from obese animals also required significantly higher adverse pressure to trigger valve closure. Importantly, when subjected to treatment with a western diet, globally deficient PAI-1 mice were significantly protected against metabolic dysfunction and displayed fully functional, competent mesenteric lymphatic valves. In conclusion, our findings show for the first time that, in association with the metabolic alterations induced by the western diet, lymphatic valve dysfunction can be a critical component of obesity-induced lymphedema.

Highlights

  • Deficient transport of lymph by a dysfunctional lymphatic system can lead to abnormal accumulation of fluid in the interstitial spaces, known as lymphedema

  • The undoubtful connection between obesity and lymphatic dysfunction has become evident by the increasing number of cases of morbidly obese patients that present with severe cases of secondary lymphedema (Farshid and Weiss, 1998; Chopra et al, 2015)

  • We recently developed a method for the assessment of lymphatic valve function (Castorena-Gonzalez et al, 2020) that allows us to determine the degree of pressure back-leak through isolated lymphatic valves when challenged with an adverse pressure gradient

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Summary

Introduction

Deficient transport of lymph by a dysfunctional lymphatic system can lead to abnormal accumulation of fluid in the interstitial spaces, known as lymphedema. It is recognized that obesity significantly increases the risk for developing secondary lymphedema. The undoubtful connection between obesity and lymphatic dysfunction has become evident by the increasing number of cases of morbidly obese patients that present with severe cases of secondary lymphedema (Farshid and Weiss, 1998; Chopra et al, 2015). Clinical studies have shown that morbidly obese patients are at significantly higher risk of developing lower-extremity lymphedema, i.e., abnormal fluid drainage, as determined by lymphoscintigraphy (Greene et al, 2012). Patients with a body mass index greater than ~50 kg/m2 have over 200-times greater odds of developing highly severe cases of lymphedema, i.e., massive localized lymphedema (Maclellan et al, 2017)

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