Abstract

The lymphatic circulation is an important component of the circulatory system in humans, playing a critical role in the transport of lymph fluid containing proteins, white blood cells, and lipids from the interstitial space to the central venous circulation. The efficient transport of lymph fluid critically relies on the rhythmic contractions of collecting lymph vessels, which function to “pump” fluid in the distal to proximal direction through the lymphatic circulation with backflow prevented by the presence of valves. When rhythmic contractions are disrupted or valves are incompetent, the loss of lymph flow results in fluid accumulation in the interstitial space and the development of lymphedema. There is growing recognition that many pharmacological agents modify the activity of ion channels and other protein structures in lymph muscle cells to disrupt the cyclic contraction and relaxation of lymph vessels, thereby compromising lymph flow and predisposing to the development of lymphedema. The effects of different medications on lymph flow can be understood by appreciating the intricate intracellular calcium signaling that underlies the contraction and relaxation cycle of collecting lymph vessels. For example, voltage-sensitive calcium influx through long-lasting (“L-type”) calcium channels mediates the rise in cytosolic calcium concentration that triggers lymph vessel contraction. Accordingly, calcium channel antagonists that are mainstay cardiovascular medications, attenuate the cyclic influx of calcium through L-type calcium channels in lymph muscle cells, thereby disrupting rhythmic contractions and compromising lymph flow. Many other classes of medications also may contribute to the formation of lymphedema by impairing lymph flow as an off-target effect. The purpose of this review is to evaluate the evidence regarding potential mechanisms of drug-related lymphedema with an emphasis on common medications administered to treat cardiovascular diseases, metabolic disorders, and cancer. Additionally, although current pharmacological approaches used to alleviate lymphedema are largely ineffective, efforts are mounting to arrive at a deeper understanding of mechanisms that regulate lymph flow as a strategy to identify novel anti-lymphedema medications. Accordingly, this review also will provide information on studies that have explored possible anti-lymphedema therapeutics.

Highlights

  • Lymphedema is a disease that impacts approximately 10 million people in the United States and hundreds of millions of individuals worldwide (Lymphatic Education and Research Network, 2019)

  • Epidemiological studies suggest that administration calcium channel blockers (CCBs) increase the risk of lymphedema (Stolarz et al, 2019a), and Class I and Class III antiarrhythmic drugs may have the potential to disrupt generation of the action potentials and rhythmic contractions in lymph muscle cells

  • The closure of voltage-gated calcium channels reduces the intracellular calcium concentration required for insulin secretion, thereby lowering circulating insulin and permitting blood glucose levels to rise toward normal levels (Ashcroft, 2005)

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Summary

INTRODUCTION

Lymphedema is a disease that impacts approximately 10 million people in the United States and hundreds of millions of individuals worldwide (Lymphatic Education and Research Network, 2019) It is a chronic debilitating condition characterized by fluid accumulation in the interstitial spaces due to insufficient lymphatic drainage that leads to swelling, pain, and discomfort (Lymphedema Side Effects of Cancer Treatment, 2021 | CDC; PDQ Supportive and Palliative Care Editorial Board, 2002; Sleigh and Manna, 2021). The collective findings from these studies provide additional strong evidence that drug-related lymphedema is a prevalent condition with many common medications implicated as risk factors. Self-care like proper skin care, and education about the disease are essential for proper management (Borman, 2018) These guidelines do not mention drug therapies that potentially may contribute to the development and maintenance of lymphedema. Current pharmacological approaches used to prevent and/or reverse lymphedema have not proven very effective, we will review studies that have evaluated diuretics, hyaluronidase, ion channel modulating agents, ketoprofen, and tacrolimus, as possible anti-lymphedema therapeutics

LYMPHATIC MUSCLE CELL PHYSIOLOGY AND EXCITABILITY
CARDIOVASCULAR AGENTS
Anti-Arrhythmic Agents
Sodium Channel Blockers (Class I)
Beta Adrenergic Receptor Blockers (Class II)
Potassium Channel Blockers (Class III)
Calcium Channel Blockers (Class IV)
Vasodilators
KATP Channel Openers
ANTI-DIABETIC AGENTS
Thiazodilinediones
CHEMOTHERAPEUTIC AGENTS
Anthracyclines
Taxanes
Corticosteroids Co-Administered With Chemotherapy
POTENTIAL THERAPIES FOR LYMPHEDEMA
Diuretics
Hyaluronidase
Ion Channel Modulating Agents
Findings
Anti-inflammatory and Immunosuppressive Agents
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