Oxidative stress‐induced methemoglobinemia is the silent killer during snakebite: a novel and strategic neutralization by melatonin. Issue 2 (14th July 2015)
- Record Type:
- Journal Article
- Title:
- Oxidative stress‐induced methemoglobinemia is the silent killer during snakebite: a novel and strategic neutralization by melatonin. Issue 2 (14th July 2015)
- Main Title:
- Oxidative stress‐induced methemoglobinemia is the silent killer during snakebite: a novel and strategic neutralization by melatonin
- Authors:
- Sharma, Rachana D.
Katkar, Gajanan D.
Sundaram, Mahalingam S.
Paul, Manoj
NaveenKumar, Somanathapura K.
Swethakumar, Basavarajaiah
Hemshekhar, Mahadevappa
Girish, Kesturu S.
Kemparaju, Kempaiah - Abstract:
- <abstract abstract-type="main" id="jpi12256-abs-0001"> <title>Abstract</title> <p>Oxidative stress‐induced methemoglobinemia remained an untouched area in venom pharmacology till date. This study for the first time explored the potential of animal venoms to oxidize hemoglobin to methemoglobin. In in vitro whole‐blood assay, methemoglobin forming ability of venoms varied as <italic>Naja naja </italic>&gt; <italic>Ophiophagus hannah </italic>&gt; <italic>Echis carinatus </italic>&gt; <italic>Daboia russellii </italic>&gt; <italic>Apis mellifera </italic>&gt; <italic>Mesobuthus tamulus </italic>&gt; <italic>Hippasa partita</italic>. Being highly potential, <italic>N</italic>. <italic>naja</italic> venom was further studied to observe methemoglobin formation in RBCs and in combinations with PMNs and PBMCs, where maximum effect was observed in RBCs + PMNs combination. <italic>Naja naja</italic> venom/externally added methemoglobin‐induced methemoglobin formation was in parallel with ROS generation in whole blood/RBCs/RBCs + PMNs/RBCs + PBMCs. In in vivo studies, the lethal dose (1 mg/kg body weight, i.p.) of <italic>N. naja</italic> venom readily induced methemoglobin formation, ROS generation, expression of inflammatory markers, and hypoxia‐inducible factor‐3<italic>α</italic>. Although the mice administered with three effective doses of antivenom recorded zero mortality; the methemoglobin and ROS levels remained high. However, one effective dose of antivenom when administered<abstract abstract-type="main" id="jpi12256-abs-0001"> <title>Abstract</title> <p>Oxidative stress‐induced methemoglobinemia remained an untouched area in venom pharmacology till date. This study for the first time explored the potential of animal venoms to oxidize hemoglobin to methemoglobin. In in vitro whole‐blood assay, methemoglobin forming ability of venoms varied as <italic>Naja naja </italic>&gt; <italic>Ophiophagus hannah </italic>&gt; <italic>Echis carinatus </italic>&gt; <italic>Daboia russellii </italic>&gt; <italic>Apis mellifera </italic>&gt; <italic>Mesobuthus tamulus </italic>&gt; <italic>Hippasa partita</italic>. Being highly potential, <italic>N</italic>. <italic>naja</italic> venom was further studied to observe methemoglobin formation in RBCs and in combinations with PMNs and PBMCs, where maximum effect was observed in RBCs + PMNs combination. <italic>Naja naja</italic> venom/externally added methemoglobin‐induced methemoglobin formation was in parallel with ROS generation in whole blood/RBCs/RBCs + PMNs/RBCs + PBMCs. In in vivo studies, the lethal dose (1 mg/kg body weight, i.p.) of <italic>N. naja</italic> venom readily induced methemoglobin formation, ROS generation, expression of inflammatory markers, and hypoxia‐inducible factor‐3<italic>α</italic>. Although the mice administered with three effective doses of antivenom recorded zero mortality; the methemoglobin and ROS levels remained high. However, one effective dose of antivenom when administered along with melatonin (1:50; venom/melatonin, w/w), not only offered 100% survival of experimental mice, but also significantly reduced methemoglobin level, and oxidative stress markers including hypoxia‐inducible factor‐3<italic>α</italic>. This study provides strong drive that, complementing melatonin would not only reduce the antivenom load, but for sure greatly increase the success rate of antivenom therapy and drastically minimize the global incidence of snakebite deaths. However, further detailed investigations are needed before translating the combined therapy towards the bed side.</p> </abstract> … (more)
- Is Part Of:
- Journal of pineal research. Volume 59:Issue 2(2015)
- Journal:
- Journal of pineal research
- Issue:
- Volume 59:Issue 2(2015)
- Issue Display:
- Volume 59, Issue 2 (2015)
- Year:
- 2015
- Volume:
- 59
- Issue:
- 2
- Issue Sort Value:
- 2015-0059-0002-0000
- Page Start:
- 240
- Page End:
- 254
- Publication Date:
- 2015-07-14
- Subjects:
- Pineal gland -- Periodicals
Pineal Gland -- Periodicals
Épiphyse (Glande)
Périodique électronique (Descripteur de forme)
Ressource Internet (Descripteur de forme)
612.492 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1600-079X ↗
http://www.blackwell-synergy.com/member/institutions/issuelist.asp?journal=jpi ↗
http://www.blackwellpublishing.com/journal.asp?ref=0742-3098&site=1 ↗
http://www.ingenta.com/journals/browse/mksg/jpi?mode=direct ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/jpi.12256 ↗
- Languages:
- English
- ISSNs:
- 0742-3098
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 5040.329000
British Library DSC - BLDSS-3PM
British Library HMNTS - ELD Digital store - Ingest File:
- 4308.xml