Abstract

Cations have generally been reported to prevent jellyfish venom-induced hemolysis through multiple mechanisms by spectrophotometry. Little attention has been paid to the potential interaction between cations and hemoglobin, potentially influencing the antagonistic effect of cations. Here, we explored the effects of five reported cations, La3+, Mn2+, Zn2+, Cu2+ and Fe2+, on a hemolytic test system and the absorbance of hemoglobin, which was further used to measure their effects on the hemolysis of tentacle extract (TE) from the jellyfish Cyanea capillata. All the cations displayed significant dose-dependent inhibitory effects on TE-induced hemolysis with various dissociation equilibrium constant (Kd) values as follows: La3+ 1.5 mM, Mn2+ 93.2 mM, Zn2+ 38.6 mM, Cu2+ 71.9 μM and Fe2+ 32.8 mM. The transparent non-selective pore blocker La3+ did not affect the absorbance of hemoglobin, while Mn2+ reduced it slightly. Other cations, including Zn2+, Cu2+ and Fe2+, greatly decreased the absorbance with Kd values of 35.9, 77.5 and 17.6 mM, respectively. After correction, the inhibitory Kd values were 1.4 mM, 45.8 mM, 128.5 μM and 53.1 mM for La3+, Zn2+, Cu2+ and Fe2+, respectively. Mn2+ did not inhibit TE-induced hemolysis. Moreover, the inhibitory extent at the maximal given dose of all cations except La3+ was also diminished. These corrected results from spectrophotometry were further confirmed by direct erythrocyte counting under microscopy. Our results indicate that the cations, except for La3+, can interfere with the absorbance of hemoglobin, which should be corrected when their inhibitory effects on hemolysis by jellyfish venoms are examined. The variation in the inhibitory effects of cations suggests that the hemolysis by jellyfish venom is mainly attributed to the formation of non-selective cation pore complexes over other potential mechanisms, such as phospholipases A2 (PLA2), polypeptides, protease and oxidation. Blocking the pore-forming complexes may be a primary strategy to improve the in vivo damage and mortality from jellyfish stings due to hemolytic toxicity.

Highlights

  • Jellyfish are free-swimming marine animals consisting of a gelatinous umbrella-shaped bell and trailing tentacles

  • It is reported that hemolysis can range from simple nuisance to serious pathological and lethal events, and is a frequent effect of a number of jellyfish venoms acting as lytic protein/peptides that alter cell permeability resulting in ion transport, cell swelling and osmotic lysis, whereas others are phospholipases inducing degradation of bilayer phospholipids or channelforming agents embedded into the membrane (Mariottini, 2014)

  • Dose-dependent tentacle extract (TE) hemolysis by spectrophotometry Using current spectrophotometric methods, we examined the dose-dependent relationship of hemolysis by TE from the jellyfish Cyanea capillata

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Summary

Introduction

Jellyfish are free-swimming marine animals consisting of a gelatinous umbrella-shaped bell and trailing tentacles. While they are found in coastal water zones worldwide, jellyfish populations fluctuate greatly in accordance with ocean climate and, perhaps, other factors related to human interactions (Williamson et al, 1984; Winter et al, 2010). The jellyfish venom in the nematocyst, to many other types of venom, is a complex mixture of bioactive proteins and peptides that have demonstrated a wide spectrum of biological activities (Bloom, Burnett & Alderslade, 1998; Chung et al, 2001; Yanagihara et al, 2002; Sanchez-Rodriguez, Torrens & Segura-Puertas, 2006; Brinkman & Burnell, 2008), including dermonecrotic, cardiotoxic, neurotoxic, hemolytic, enzymatic, immunogenic and inflammatory effects. It is reported that hemolysis can range from simple nuisance to serious pathological and lethal events, and is a frequent effect of a number of jellyfish venoms acting as lytic protein/peptides that alter cell permeability resulting in ion transport, cell swelling and osmotic lysis, whereas others are phospholipases inducing degradation of bilayer phospholipids or channelforming agents embedded into the membrane (Mariottini, 2014)

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