Abstract

Suramin has long been used in the treatment of various human diseases. Intravenous infusions of Suramin are commonly administered to patients over extended periods of time but there are a number of significant contraindications with peripheral muscle weakness being one of the most frequently reported. Previous work has shown that even after a single infusion (300 mg kg−1) Suramin remains in skeletal muscle in effective concentrations (11.6 μg mL −1; 84 days) for prolonged periods. These observations provide a strong rationale for investigation of the specific effects of Suramin on skeletal muscle function. Single mechanically skinned fibers were directly exposed to Suramin (10, 100 or 500 μmol L−1) for defined durations (2–10 min) in controlled physiological solutions that mimic the intracellular ionic environment of a fiber. Suramin treatment (10–500 μmol L−1) directly affected the contractile apparatus in a dose‐dependent manner causing a decrease in Ca2+‐sensitivity (pCa50 = −log (Ca2+) concentration, where 50% of maximum Ca2+‐ activated force is produced) by 0.14 to 0.42 pCa units and reduction in maximum Ca2+‐activated force by 14 to 62%. Suramin treatment (100 μmol L−1 for 10 min and 500 μmol L−1 for 2 min) also caused development of a Ca2+‐independent force corresponding to 2.89 ± 4.33 and 16.77 ± 7.50% of pretreatment maximum Ca2+‐activated force, respectively. Suramin treatment (100 μmol L−1, 2 min) also increased the rate of sarcoplasmic reticulum (SR) Ca2+ release without significant changes in SR Ca2+ uptake. We report new functional effects for Suramin related to alterations in both the contractile apparatus and SR Ca2+‐handling of skeletal muscle that may contribute to the peripheral muscle weakness noted in human pharmacological treatments.

Highlights

  • Suramin is a broad acting polyanionic compound that has been used over many decades, initially for the treatment of African sleeping sickness (African trypanosomiasis) (Reincke et al 1994; Joshi et al 2005) and subsequently for river blindness due to onchocerciasis (Schulz-Key et al 1985)

  • We report new functional effects for Suramin related to alterations in both the contractile apparatus and sarcoplasmic reticulum (SR) Ca2+-handling of skeletal muscle that may contribute to the peripheral muscle weakness noted in human pharmacological treatments

  • A novel finding of this study was the marked effect of Suramin on the functions of the contractile apparatus and Ca2+-regulatory system

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Summary

Introduction

Suramin is a broad acting polyanionic compound that has been used over many decades, initially for the treatment of African sleeping sickness (African trypanosomiasis) (Reincke et al 1994; Joshi et al 2005) and subsequently for river blindness due to onchocerciasis (Schulz-Key et al 1985). More recently it has become a treatment modality for adults with recurrent high-grade gliomas (Takano et al 1994; Grossman et al 2001). Among the most significant side effects are severe fatigue, malaise and lethargy, which all may be manifest as a broad spectrum neuromuscular peripheral weakness of the hands, arms, legs and feet of patients

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