Literature DB >> 21821138

Target organ identification of jellyfish envenomation using systemic and integrative analyses in anesthetized dogs.

Changkeun Kang1, Young Ki Kim, Hyunkyoung Lee, Mijin Cha, Eun-Tae Sohn, Eun-Sun Jung, Chiyoun Song, Minkyung Kim, Hee Chun Lee, Jong-Shu Kim, Jin-Yong Hwang, Won Duk Yoon, Euikyung Kim.   

Abstract

Proper treatment of jellyfish envenomed patients can be successfully achieved only from an understanding of the overall functional changes and alterations in physiological parameters under its envenomation. The majority of previous investigations on jellyfish venoms have covered only a couple of parameters at a time. Unlike most other fragmentary jellyfish studies, we employed an integrative toxicological approach, including hemodynamics, clinical chemistry and hematology analyses, using N. nomurai jellyfish venom (NnV) in dogs. After the baseline measurements for mean arterial pressure (MAP), cardiac output (CO) and heart rate (HR), NnV was intravenously administered to the dogs at doses of 0.1 or 0.3mg/kg body weight. The dogs showed significant decreases in MAP (-27.4±3.7 and -48.1±9.9 mmHg), CO (-1.1±0.1 L/min and -1.0±0.2 L/min), and HR (-4.5±0.3 and -9.9±3.1 beats/min) comparing with the respective baseline controls. The onset of systemic hypotension and bradycardia occurred within 1 min of NnV injection and they lasted for 1-35 min, depending on the NnV doses. Interestingly, serum biochemical analyses of envenomed dogs exhibited dramatic increases of alkaline phosphatase (ALP), creatine phosphokinase (CPK), alanine aminotransferase (ALT) and aspartate aminotransferase (AST), indicating its possible target organs. In conclusion, we have demonstrated simultaneously, for the first time, the multiple organ toxicities (cardiotoxic, myotoxic and hepatotoxic) of a scyphozoan jellyfish venom. Based on these results, an integrative toxinological approach using dogs appears to be effective in predicting jellyfish venom toxicities and designing their therapeutic strategies. We expect this method can be applied to other jellyfish venom research as well.
Copyright © 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 21821138     DOI: 10.1016/j.vascn.2011.07.004

Source DB:  PubMed          Journal:  J Pharmacol Toxicol Methods        ISSN: 1056-8719            Impact factor:   1.950


  4 in total

1.  Cloning a Chymotrypsin-Like 1 (CTRL-1) Protease cDNA from the Jellyfish Nemopilema nomurai.

Authors:  Yunwi Heo; Young Chul Kwon; Seong Kyeong Bae; Duhyeon Hwang; Hye Ryeon Yang; Indu Choudhary; Hyunkyoung Lee; Seungshic Yum; Kyoungsoon Shin; Won Duk Yoon; Changkeun Kang; Euikyung Kim
Journal:  Toxins (Basel)       Date:  2016-07-05       Impact factor: 4.546

2.  In vitro characterization of jellyfish venom fibrin(ogen)olytic enzymes from Nemopilema nomurai.

Authors:  Seong Kyeong Bae; Hyunkyoung Lee; Yunwi Heo; Min Jung Pyo; Indu Choudhary; Chang Hoon Han; Won Duk Yoon; Changkeun Kang; Euikyung Kim
Journal:  J Venom Anim Toxins Incl Trop Dis       Date:  2017-07-19

3.  Proteomic Analysis of Novel Components of Nemopilema nomurai Jellyfish Venom: Deciphering the Mode of Action.

Authors:  Indu Choudhary; Du Hyeon Hwang; Hyunkyoung Lee; Won Duk Yoon; Jinho Chae; Chang Hoon Han; Seungshic Yum; Changkeun Kang; Euikyung Kim
Journal:  Toxins (Basel)       Date:  2019-03-08       Impact factor: 4.546

4.  protective effect of tetracycline against dermal toxicity induced by Jellyfish venom.

Authors:  Changkeun Kang; Yeung Bae Jin; Jeongsoo Kwak; Hongseok Jung; Won Duk Yoon; Tae-Jin Yoon; Jong-Shu Kim; Euikyung Kim
Journal:  PLoS One       Date:  2013-03-11       Impact factor: 3.240

  4 in total

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