1.Influence of some Factors on Ribonucleolytic Activity of Black Cobra Venom
Journal of Medicinal Materials - Hanoi 2003;8(4):118-122
Among the enzymes found in snake venom, ribonuclease (RNase) has been known to have the potential effect against cancer and HIV. In a previous report, the author and his colleague have demonstrated that RNase from Vietnamese black cobra (Naja naja) venom differed from all the other identified RNase for its extremely low optimal value of pH. The results in this study showed that it also differed in nonlinear activity dependence on the enzyme concentrations and a sigmoidal curve of saturation with the substrate. This enzyme expressed the maximal activity at the ionic strength of 10 mM of the reaction buffers. Ammonium sulfate entirely suppressed the enzyme activity at the concentration over 70 mM, and sodium chloride reduced the activity by 70% at the level over 100 mM. No magnesium ion was needed for the activation of this RNase.
Snake Venoms
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Snakes
;
Animals, Poisonous
;
Black Cobra Venom
2.Transcriptome analysis of venom gland and identification of functional genes for snake venom protein in Agkistrodon acutus.
Sheng-Xiang ZHANG ; Yuan-Yuan SHI ; Chun-Miao SHAN ; Tao WANG ; Zhen-Xing WANG ; Sheng-Song WANG ; Jia-Wen WU
China Journal of Chinese Materia Medica 2019;44(22):4820-4829
Agkistrodon acutus is a traditional Chinese herb medicine which has immunological regulation,anti-tumor,anti-inflammatory and analgesic effects,which is mainly used for the treatment of rheumatoid arthritis,ankylosing spondylitis,sjogren's syndrome and tumors. In order to excavate more important functional genes from A. acutus,the transcriptome of the venom gland was sequenced by the Illumina Hi Seq 4000,and 32 862 unigenes were assembled. Among them,26 589 unigenes were mapped to least one public database. 2 695 unigenes were annotated and assigned to 62 TF families,and 5 920 SSR loci were identified. The majority of mapped unigenes was from Protobothrops mucrosquamatus in the NR database,which revealed their closest homology. Three secretory phospholipase A_2 with different amino acid sequences showed similar spatial structures and all had well-conserved active sites. The 3 D structural models of C-type lectin showed conserved glycosylation binding sites( Asn45). This study will lay the foundation for the further study of the function of snake venom protein,and promoting the development and utilization of genome resources from A. acutus.
Agkistrodon/genetics*
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Animals
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Crotalid Venoms
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Gene Expression Profiling
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Snake Venoms/genetics*
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Snakes
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Transcriptome
3.Polymorphism of Black Snake Venom RNase.I - Two distinct kinetical forms
Pharmaceutical Journal 2003;0(6):167-170
In the study, using the kinetic method for the examination of the dependence between the specific activity of the enzyme and the concentration of the enzyme itself in the combined reaction, the researchers have proved that the Ribonuclease (R.Nase) molecule of the black cobra (Naja naja) venom exits at least in two interconvertible forms with the difference in specific activity of almost one grade. These two forms are probably the different oligomers or configurations, temporarily named as the kinetic forms of R.Nase found in the black cobra venom.
Snake Venoms
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Ribonucleases
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Polymorphism, Genetic
4.Isolated ocular injury due to spitting cobra's venom
Azimuddin Azim SIRAJ ; Nayan JOSHI
Brunei International Medical Journal 2012;8(3):145-148
Some species of venomous snakes spit venom in human eyes as a defence mechanism when threatened. If not detected and treated appropriately early, this can result in severe toxic ocular injury leading to potential blindness (snake venom ophthalmia). Not much is known of the clinical course and treatment guidelines due to the rarity of such occurrences. We present a case of isolated severe toxic ocular injury in one eye who reported to us with very poor vision following venom spit, which was promptly treated leading to a successful visual recovery. This is the first documented case of snake venom ophthalmia from Kuala Belait, Brunei Darussalam.
Elapidae
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Snake Venoms
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Corneal Opacity
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Blindness
5.Anti-proliferative Effects of Androctonus amoreuxi Scorpion and Cerastes cerastes Snake Venoms on Human Prostate Cancer Cells.
Hassan AKEF ; Nahla KOTB ; Dina ABO-ELMATTY ; Sayed SALEM
Journal of Cancer Prevention 2017;22(1):40-46
The present study evaluated the effects of Androctonus amoreuxi scorpion venom, Cerastes cerastes snake venom and their mixture on prostate cancer cells (PC3). An MTT assay was used to determine the anti-proliferative effect of the venoms, while quantitative real time PCR was used to evaluate the expression of apoptosis-related genes (Bax and Bcl-2). Furthermore, colorimetric assays were used to measure the levels of malondialdehyde (MDA) and antioxidant enzymes. Our results show that the venoms significantly reduced PC3 cell viability in a dose-dependent manner. On the other hand, these venoms significantly decreased Bcl-2 gene expression. Additionally, C. cerastes venom significantly reduced Bax gene expression, while A. amoreuxi venom and a mixture of A. amoreuxi & C. cerastes venoms did not alter Bax expression. Consequently, these venoms significantly increased the Bax/Bcl-2 ratio and the oxidative stress biomarker MDA. Furthermore, these venoms also increased the activity levels of the antioxidant enzymes, catalase, superoxide dismutase, glutathione peroxidase, glutathione reductase, and glutathione-S-transferase. Overall, the venoms have cytotoxic and anti-proliferative effects on PC3 cells.
Apoptosis
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Catalase
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Cell Survival
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Gene Expression
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Genes, bcl-2
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Glutathione Peroxidase
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Glutathione Reductase
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Hand
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Humans*
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Malondialdehyde
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Oxidative Stress
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Prostate*
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Prostatic Neoplasms*
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Real-Time Polymerase Chain Reaction
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Scorpion Venoms
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Scorpions*
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Snake Venoms*
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Snakes*
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Superoxide Dismutase
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Venoms
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Viper Venoms
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Viperidae*
6.The History of Myasthenia Gravis.
Journal of the Korean Neurological Association 2009;27(2):98-104
Since Willis described 'fatigable weakness' in 1672, most physicians consider it as a kind of hysteria due to the inconsistent fluctuation of symptoms. Erb presented three cases of 'bulbal palsy' in the 1870s, and Oppenheim and Hopper considered myasthenia gravis as a disease similar to curare poisoning and as a disease induced by attack of the motor centers by intrinsic toxins, respectively. In 1903, Elliot suggested that a 'chemical substance' mediates the nerve impulses at synapse. However, it was not until 1921 that this was demonstrated by Loewi, who provided evidence from the famous two-frog-hearts experiment. Dale later revealed the substance to be acetylcholine, and he also suggested that myasthenia gravis is due to a problem with the motor end plate. In 1934, Walker was prompted by the resemblance between myasthenia gravis and curare poisoning to apply physostigmine, a curare-poisoning antidote, to a patient, which produced a dramatic result. Since then the use of anticholinesterase inhibitors has been adopted for standard therapeutic modality. Some prominent surgeons have also applied thymectomy as a surgical modality. The most recent focus of myasthenia gravis has been immunological. In 1960, Simpson proposed the autoimmune hypothesis, and Chang et al. showed that snake venom contained a selective antagonist of the nicotinic acetylcholine receptor, alpha-bungarotoxin. The immunization of rabbits with acetylcholine receptor purified from the electrical organs of electric eels by Patrick et al. induced myasthenic symptoms and signs, and these were reversed by acetylcholinesterase inhibitors. The role of the autoimmune system has led to the introduction of an immunosuppressive modality and plasma exchange to the field of clinical neurology.
Acetylcholine
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Action Potentials
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Bungarotoxins
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Cholinesterase Inhibitors
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Curare
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Electrophorus
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History of Medicine
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Humans
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Hysteria
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Immunization
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Motor Endplate
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Myasthenia Gravis
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Physostigmine
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Plasma Exchange
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Rabbits
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Receptors, Nicotinic
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Snake Venoms
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Synapses
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Thymectomy
7.Hematological Features of Coagulopathy and the Efficacy of Antivenin Therapy for a Korean Snakebite.
Byoung Joon LEE ; Sung Il HONG ; Hae Sung KIM ; Tae Hwa KIM ; Jeong Hoon LEE ; Han Joon KIM ; Byoung Yoon RYU ; Hong Ki KIM
Journal of the Korean Surgical Society 2007;72(1):18-26
PURPOSE: Snake venom induced coagulopathy is a major cause of both morbidity and mortality among affected patients. The effects of venomous factors to coagulation cascade and fibrinolysis were verified by analyzing the hematological data and clinical features of envenomed patients, and the efficacy of blood products transfusion and antivenin against a Korean snakebite clarified. METHODS: A retrospective study was conducted on 57 patients, admitted to the Department of Surgery of Chuncheon Sacred Hospital, between July 2002 and October 2005. According to the guidelines for assessing the severity of North American envenomination, the patients were divided into three groups according to severity, and the clinical course, DIC profile and usages of blood products and antivenin then analyzed. RESULTS: Of the 15 patients in the severe group (26.3%), 9 (60.0%) developed severe coagulation abnormalities, similar to DIC. No substantial bleeding or thrombic event manifested. All the patients with initial hypofibrinogenemia (33.3%) and unmeasured PT/aPTT during the 2nd to 4th hospital days (46.7%) progressed to severe coagulopathy. On average, these patients received transfusions of 18.4 +/- 6.1 pints of FFP and 14.4 +/- 14.9 pints of platelet product. The average amounts of antivenin applied were 1.2 +/- 0.4, 1.7 +/- 0.5 and 2.8 +/- 0.8 vials for the Minimal, Moderate and Severe groups, respectively. There was no death due to a Korean snakebite during this period. CONCLUSION: Korean snake venom is assumed to be a complex mixture of anticoagulant, platelet active and fibrinolytic venom. The discrepancy between abnormal coagulopathy and the clinical course explains venom induced DIC-like syndrome. Hypofibrinogenemia is the most reasonable predictor of DIC-like syndrome. Abrupt prolongation of PT/aPTT during the 2nd to 4th hospital days must weigh against thrombocytopenia. An early antivenin injection, along with the proper use of blood products, could improve the clinical course of envenomed patients.
Blood Platelets
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Dacarbazine
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Fibrinolysis
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Gangwon-do
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Hemorrhage
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Humans
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Mortality
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Retrospective Studies
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Snake Bites*
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Snake Venoms
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Thrombocytopenia
;
Venoms
8.A case report of Naja atra bitten poisoning in northern China.
Ping HAN ; Si-zhuo PANG ; Xiang-dong GUAN ; Jie-ru WANG
Chinese Journal of Industrial Hygiene and Occupational Diseases 2013;31(9):706-706
Animals
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China
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Elapidae
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Humans
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Male
;
Snake Bites
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Snake Venoms
;
poisoning
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Young Adult
9.Effect of Snake Venom: Arginine-esterase on the Fibrinolytic Activity.
Jung Min PARK ; Jae Whan LIM ; Hyung Kook PARK ; Ki Bum SUNG ; Moo Young AHN ; Hyun Kil SHIN
Journal of the Korean Neurological Association 1995;13(3):464-472
BACKGROUND AND PURPOSE: Arginine esterase(Ancrod), a thrombin-like enzyme, purified from the venoms of Agkistrodon halys, has known to cleave fibrinopeptide A from the fibrinogen and lead to circulation of soluble noncross-linked "ancrodfibrin', which stimulates endogenous T-PA release.Many authors have suggested clinical applicability of this enzyme,but clinical studies on its fibrinolytic action has been insufficient.Thus we studied the influence of this enzyme on fibrinolytic activity in cerebral infarction. METHOD: We observed the change of euglobulin fibrinolytic activity, t-PA antigen, t-PA activity, fibrinopeptide A, fibrinogen, FDP and D-dimer, during 12 hours after a bolus intravenous administration of 0.25 unit of the arginine esterase to the 9 patients with cerebral infarction. RESULT:There was no change of the euglobulin fibrinolytic activity, fibrinopeptide A and t-PA Ag but there was significant increase in both t-PA activity and FDP, D-dimer and significant decrease in fibrinogen. CONCLUSION: Our result suggest that arginine esterase converts fibrinogen to a fibrin polymer which has a increased susceptibility to lysis by plasmirl This enzyme seems to amplify T-PA activity through the consequent increase in FT)P, because there is no increase in the euglobulin fibrinolytic activity, fibr'mopeptide A and t-PA Ag suggesting direct T-PA release. Arginine esterase, having action of effective defibrinogenation and safe fibrinolysis,could be used for the thrombus related disease.
Administration, Intravenous
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Agkistrodon
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Arginine
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Cerebral Infarction
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Fibrin
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Fibrinogen
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Fibrinopeptide A
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Humans
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Polymers
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Snake Venoms*
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Snakes*
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Thrombosis
;
Venoms
10.Optimal Dose of Antivenin for Asymptomatic or Minor Envenomation Patient with Korean Viperidae Injuries.
Kyoung Min YOU ; Woon Young KWON ; Tae Hyeong KWON ; Jong Hwan SHIN ; Hui Jai LEE
Journal of the Korean Society of Emergency Medicine 2013;24(4):420-427
PURPOSE: The aim of this study was to evaluate the feasibility and safety of our antivenin treatment protocol for patients with Korean Viperidae envenomation. METHODS: We developed an antivenin treatment protocol for Korean Viperidae envenomation, based on previous data, and applied this treatment to the enrolled patients. In brief, antivenin was not used for patients with grade 0. Patients with grade I and II received one vial of antivenin. Those with grade III and IV received two and three vials of antivenin, respectively. Adult patients who visited the emergency department (ED) after receiving a snakebite between July 2008 to August 2010 were included. Follow ups were performed at 24 hours, 7 days, and 28 days after the snakebite. RESULTS: A total of 62 patients were enrolled. At the initial evaluation, 6 patients (9.7%) were grade 0, 47 patients (75.8%) were grade I, and 9 patients (14.5%) were grade II. Upon the follow-up evaluation, 14 patients (29.8%) progressed from grade I to grade II and 2 patients (22.2%) progressed from grade II to III. Coagulopathy developed in 5 patients (8.0%) and rhabdomyolysis in 5 patients (8.0%). Urticaria developed in 2 patients (3.2%) and cellulitis in 3 patients (4.8%) as delayed complications. As an antivenin-related complication, serum sickness developed in only 1 patient (1.6%). There were no severe complications and all clinical and laboratory abnormalities disappeared within 28 days. CONCLUSION: Our antivenin treatment protocol was feasible and safe. To confirm our data, multicenter validation studies are needed.
Adult
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Antivenins
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Cellulitis
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Clinical Protocols
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Emergencies
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Follow-Up Studies
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Humans
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Rhabdomyolysis
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Serum Sickness
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Snake Bites
;
Snake Venoms
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Urticaria
;
Viperidae