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Haematological Effects of Odontobuthus odonturus (Arachnida: Buthidae) Venom in Albino Mice.

Byline: Rabia Mishal, Hafiz Muhammad Tahir, Rabia Yaqoob, Kinza Zafar, Muhammad Arshad and Muhammad Sher

Abstract

Scorpion envenomation represents a significant cause of morbidity and mortality in many countries. Odontobuthus odonturus is a medically important scorpion that inhibits sandy areas. In the present study we evaluated the in-vivo toxic effects of O. odonturus venom on male albino mice. Scorpions were collected from undisturbed sandy areas of district Sargodha (Punjab), Pakistan. We extracted the venom and injected intraperitoneally into healthy albino mice. Haemato-pathological effects of the venom were studied on different blood parameters i.e., total leucocyte count (TLC), neutrophil count, RBC's count and platelet count, lymphocytes, eosinophils and monocytes. The venom of O. odonturus caused drastic change in blood physiology of treated animals. We observed a significant decrease in RBC's, platelets and lymphocyts of treated animals. However, treated animals showed marked increased in neutrophils, hemoglobin and TLC count.

There was no difference in the count of monocytes and eosinophils between treated and control animals. It is concluded from the study that venom of O. odonturus is potentially harmful to mammals as it badly affects the blood physiology which may ultimately leads towards many disorders in the body.

Keywords: Odontobuthus odonturus, venom, haematological studies, toxicity, blood physiology.

INTRODUCTION

Scorpions are venomous arachnids with highly conserved morphology (Murthy and Krishina 2002; Ruming et al., 2010). They occupied tropical and subtropical areas and found everywhere except Antarctica (Isbester et al., 2003; Petricevich, 2010). They have potential to bear very drastic environmental conditions; therefore, they are very successful invertebrates (Zlotkin et al., 2001). Till now 16 scorpion families and approximately 1500 scorpion species and sub-species have been discovered (Bawaskar and Bawaskar, 2012). Amongst all families Buthidae is considered as the most poisonous and medically important (Chowell et al., 2006; Michael and Victor, 2003).

Scorpion venom is a rich source of biochemically activated enzymes, amines and low molecular weight peptides (Gomez et al., 2010). Till now 400 peptides have been isolated from scorpion venom (Shirmardi et al., 2010). These peptides range in mass from 1,000 to 9,000 Da (Rates et al., 2008; Schwartz et al., 2007) and mainly target sodium, potassium, calcium (Choung et al., 1998) and chloride channels (Possani et al., 2000). Scorpion venom also has tremendous ability to inhibit or activate the ion channels, acetylcholine receptors, acetylcholine esterase, membranes coagulation and anticoagulation pathways with highly selective affinity (Bogin, 2005; Jalali et al., 2012).

On the basis of molecular weight scorpion toxins are divided into two classes. The first class contains 60-70 amino acids cross linked by four disulfide bridges (Gordon et al., 2003). They are exclusive for sodium channels of excitable cells (Rochet et al., 1979). The second class contains 30-40 amino acids cross linked by three or four disulfide bridges (Kharrat et al., 1997). These are single chained toxins and due to their binding activities these have been described as a or AY toxins. Their particular target site is K+ channels and calcium activated K+ (Rodriguez and Possani, 2005).

Envanomation by the scorpions is very common in rural areas (Ozkan et al., 2011). Toxic peptides of scorpion venom may cause death of their victims (Mirakabadi et al., 2006). Scorpion venom also exhibits various other effects like, hemolytic (Cournet et al., 1994), muscular effect (Jalali et al., 2007; Vatanpour et al., 2012), renal failure (De Sousa et al., 2005), cardiovascular failure (Bakir et al., 2012), pulmonary oedema and respiratory arrest (Ozkan and Carhan, 2008). Scorpion's bites may induce myocarditis and left ventricular hypertrophy due to long standing hyper tension (Sarakar et al., 2008). More than 70% people suffer from gastrointestinal manifestation after scorpion stung (Deshpande et al., 2005). Scorpion venom also causes pulmonary (Amaral and Rezende, 1997; Coelho and Pessini, 2007) and renal oedema (De Sousa et al., 2005; Severino et al., 2009).

Present study was aimed at investigating the in-vivo hematological effects of Odontobuthus odonturus venom on male albino mice. Outcome of the study will be helpful in devising better curative strategies against bites of venous scorpions of the area.

MATERIALS AND METHODS

Scorpion collection

The study was conducted at the Department of Zoology, University of Sargodha, Pakistan from May 2012 to April 2013. Healthy and adult scorpions were collected from undisturbed sandy areas of district Sargodha (32.083N; 72.671E), using portable ultraviolet (UV) lamps at night. Scorpion collection was done during no moon cycle period of month.

Venom extraction and sample preparation

The venom was extracted by electrical stimulation (20 MV). Platinum electrode was used for electric stimulation to extract the venom from the swollen telsons of scorpions. The milking process continued as long as was necessary, usually between 10-15 seconds. The venom was collected in Eppendorf tubes (1.5 ml) and stored at -20C for later use.

The lyophilized dried venom (60mg) was dissolved in 900l double distilled water and kept for 48 h at 4C (Masihipour, 2005). After dialysis, venom was centrifuged at 14,000 rpm for 10 min at 4C. Mucous material and un-dissolved residues were separated apart and the supernatant was collected in Eppendorf tubes (1.5ml).

Experimental protocol

The toxicity of the O. odonturus venom was determined on Stock Webster strain of albino mice, Mus musculus.

Twenty five healthy adult male albino mice, Webstar strain, Mus musculus with an average weight between 25-30 g were used in the study. All the animals were housed in different cages under controlled light (325 lux), humidity (40-50%) and temperature (26-32C). They were fed with standard diet.

Four doses i.e., 120, 170, 200 and 250l of stock solution (60mg/900l double distilled water) were used to test the toxicity in this experiment. Five groups each of 5 albino mice were used. The first group was kept as control and given normal diet (unmarked), whereas the remaining four groups (each of 5 albino mice) were administered with venom intraperitoneally at 120, 170, 200 and 250 l using insulin syringes. All groups were placed separately under observation for 24 h.

After 24 h, mice were anesthetized with chloroform, sacrificed and blood was drawn directly from heart using 1 ml syringe. The blood was stored in EDTA coated tubes and used for total leukocyte count (TLC), RBC's count, neutrophils, eosinophils, monocytes, lymphocytes and platelet count and determination of haemoglobin level. The departmental ethical committee granted permission to conduct the experiment.

Statistical analyses

One way analysis of variance (ANOVA), followed by Tukey's test, was applied by using SPSS (13) to compare the blood parameters of different groups. Differences were considered significant when P-values were less than 0.05.

RESULTS

The inflammation at the injection site, restlessness, increased urination and fecal discharge were noticed only in the treated groups. All the members of fifth group, which was injected with highest dose (i.e., 250l) were paralyzed after 12 h and died after 18 h.

Table I shows the various haematological parameter of mice after treatment with different doses of venom. The total number of RBCs decreased significantly in the treated groups (F3,16=7.99; P= 0.002), whereas, TLC increased with the increase in venom concentration (F3,16= 7.06; P=0.003). The amount of neutrophils were considerably higher in the treated groups compared to the control (F3,16 = 13.35; P= 0.001). The percentage of lymphocytes and platelets and hemoglobin level decreased significantly among treated animals (F3,16 = 13.35; P= 0.004 for lymphocytes, F3,16= 19.01; P= 0.001 for platelets and F3,16= 14.67; P= 0.011 for hemoglobin). Non-significant differences were recorded for monocytes and eosinophils (F3,16= 0.97; P= 0.445 and F3,16=0.667; P= 0.58 respectively.

Table I.-Effect of crude venom of Odontobuthus odonturus on different blood parameters of Mus musculus.

###Blood parameters

###Total

###White blood cells (WBCs)

Dose###RBCs###Platelet count###Haemoglobin

###TLC###Neutrophils###Lymphocytes###Eosinophils###Monocytes

###(1x106/l)###(1x108/l)###(g/dl)

###(1x103/l)###(%)###(%)###(%)###(%)

Control###8.990.40 b###2.260.10 a###12.0 1.70a###87.42.73 b###1.00.00 a###2.00.00 a###1103.6031.66d###8.940.40a

120 l###6.600.69 a###2.720.25ab###27.03.83b###53.05.35 a###1.00.00 a###1.60.20 a###880.80 70.07c###9.640.38b

170 l###6.600.50 a###3.540.23 b###36.22.51b###52.86.46 a###1.20.20 a###1.80.24 a###788.2091.89ab###10.060.39b

200 l###5.680.34 a###3.500.13 b###34.63.93b###49.64.20 a###1.20.20 a###1.60.24 a###704.6047.09a###12.380.36c

DISCUSSION

Most of the scorpions of family buthidae are medically important as their venom is highly toxic (Gwee et al., 2002; Mebs, 2002). Peptides of scorpions are more poisonous and dangerous than that of the snake toxins (Sofer and Gueron, 1990). Scorpion's toxins act particularly at the voltage gated sodium and potassium ion channels in the excitable nerve cells. Therefore, they can easily kill their pray and predator (Adiguzel, 2010). Envenomation by the scorpions of buthidae family causes respiratory distress, tachycardia, tachypnea, sialorrhoea and myocarditis. Scorpion venom also causes hemorrhage, severe and mild necrosis and congestion (Deghani et al., 2004).

Dehghani et al. (2012) and Abdoon and Fatani (2009) reported considerable decrease in hematocrit and RBC's count after envenomation by scorpion venom. Their finding is in accordance with our results, that all the envenomed groups showed significant decrease in total RBC's count compared to the control group. It suggests that envenomation induced hemolysis of RBC's. The venom of O. odonturus was abstemiously poisonous because at 250 l dose all the intraparitoneally treated mice were died. Emam et al. (2008) recorded about 48.73% erythrocytes hemolysis in a scorpion envenomed persons. The venom of genus Odontobuthus is highly toxic for the blood vessels (Klassen and Watkins, 2003). According to Farzanpey (1994) scorpion stung modulates hemolytic symptoms of their victim's body. Pipelzadeh et al. (2007) and Jalali et al. (2012) also observed a rapid drop in hematocrit and preferential increased hemolysis in the victim of scorpions.

Similarly, Emam et al. (2008) also reported the decreased hematocrit and considerable reduction in the RBC's number in the scorpion stung patients. Histopethological changes recoded by Zayerzadeh et al. (2010) after injecting venom were myocytolysis (lysis of myocytes), coagulation necrosis, focal hemorrhage, thrombus formation both in myocardium and on endocardial surfaces.

In the present study significant increase im average TLC count after intraperitoneal treatment was observed. Results are in accordance with Dehghani et al. (2012) and Chitnis et al. (1993), they also found elevated number of WBC's in the envenomed people. This leads towards the leukocytosis after envenomation. Significant diminution in lymphocytes was observed in intraperitoneally treated groups. However, non-significant difference in the count of eosiniphils and monocytes was recorded.

The level of neutophils increased more than twice in treated animals compared to the control. Altenburg et al. (1997) elucidated that injection of scorpion venom cause mobilization of neutrophils from the bone marrow to the blood circulation in rats that caused neutrophilia which explained the release of norepinephrine and its action on a1-adrenoceptors. Borges et al. (2000) reported that number of neutrophils circulating in the blood stream after envenomation by scorpions increased, while matured neutrophils simultaneously decreased. These increased neutrophils may participate in the propagation of lung injury in children and older age people. Neutrophilic leukocytosis attributed by scorpion envenomation has previously been studied in humans (Gueron et al., 1993; Bucaretchi et al., 1995) and animals (Cordeiro et al., 2006).

The platelet count in the present study decreased markedly which is in concurrence with Pinto et al. (2010). However, in controversy to our findings Emam et al. (2008) reported 61.4% increase of platelet count due to action of scorpion poison. According to Heemskerk et al. (2002) blood platelets impart promising role in the regulation of adhesive and coagulation properties and confers a primary physical barrier necessary to arrest the bleeding. Moreover, they provide a catalytic surface by assembling the enzymes complexes and catalytic cascades and also accelerate the fibrin formation. This alteration is consequent for the occurrence of pulmonary hemorrhage and thrombocytopenia which is reported by Longenecker and Longenecker, (1981). CorrAa et al. (1997) observed hemorrhagic lesions in the heart, lungs, and kidneys of rats after poisoning with Tityus serrulatus venom.

The level of hemoglobin in the intraperitoneally treated animals was also increased with venom dose. This increase in hemoglobin is probably due to excessive hemolysis of erythrocytes (Shahbazzadeh et al., 2007). Furthermore, increase in hemolysis of erythrocytes may increase the amount of bilirubin which may leads towards hemoglobinuria. Emen et al. (2008) confirmed the presence of hematuria in the envenomed animals and negative effect of scorpion poison on the kidney and damage to the capillary system of glumeruli. On the other hand, Nunan et al. (2003) and Nunan et al. (2004) have showed in histo-pathological studies that venom caused glumerolar congestion, dilated vessels of interstitium and focal interstitial congestion in kidneys of all animals.

CONCLUSIONS

It is concluded that scorpion venom cause drastic changes in the blood physiology which may leads to towards renal failure, hemolytic anemia by erythrocytes fragmentation, vasoconstriction in blood vessels, haemoglobinuria, pulmonary oedema, myocarditis and thromboleukopenia. In the present study we first time reported the toxicity of venom of O. odonturus. More research is needed so that effective and improved treatments for scorpion venom manifestations can be designed.

ACKNOWLEDGEMENTS

This project was supported by the University of Sargodha, Sargodha. We are thankful to Mr. Muhammad Muhsin Ahsan for his help in scorpion collection. We are also thankful to Dr. Kawaja Raees Ahmed and Mr. Tahir Abbas for their technical assistance during the experiments.

REFERENCES

ABDOON, N. A. AND FATANI, A. J., 2009. Correlation between blood pressure, cytokines and nitric oxide in conscious rabbits injected with Leiurus quinquestriatus quinquestriatus scorpion venom. Toxicon, 15: 471-480.

ADIGUZEL, S., 2010. In vivo and in vitro effects of scorpion venoms in Turkey: a mini-review. J. Venom. Anim. Toxins. Trop. Dist., 16: 198-211.

ALTENBURG, S. P., MARTINS, M. A., SILVA, R. A., CORDEIRO, R. S. B. AND CASTRO-FARIA-NETO, H.C., 1997. LPS-induced blood neutrophilia is inhibited by a1-adrenoceptor antagonists: a role for catecholamines. J. Leukocyt. Biol., 61: 689694.

AMARAL, C.F. AND REZENDE, N.A., 1997. Both cardiogenic and non-cardiogenic factors are involved in the pathogenesis of pulmonary oedema after scorpion envenoming. Toxicon, 35: 997-998.

BAKIR, F., OZKAN, O., ALCIGIR, M. E. AND VURAL, S. A., 2012. Effect of Androctonus carassicauda on heart tissue. J. Anim. Vet. Adv., 11: 2594-2599.

BAWASKAR, H. S. AND BAWASKAR, H. P., 2012. Scorpion Sting: Update. J. Assoc. Phys. India, 60: 46-53.

BOGIN, O., 2005. Venom peptides and their mimetics as potential druds. Modulator, 19: 14-20.

BORGES, C.M., SILVEIRA, M.R., APARECIDA, M., BEKER, C.L., FREIRE-MAIA, L. AND TEIXEIRA, M.M., 2000. Scorpion venom-induced neutrophilia is inhibited by a PAF receptor antagonist in the rat. J. Leukocyt. Biol., 67: 515-9.

BUCARETCHI, F., BARACAT, E., NOGUEIRA, R. N. AND ZAMBRONE, F. A. D., 1995. Severe scorpion envenomation in children: a comparison between Tityus bahiensis and Tityus serrulatus. Rev Inst Med Trop SAPound o Paulo, 37: 331-336.

CHITNIS, P. A., MARAGHI, S. AND VAZIRIANZADEH, B., 1993. Epidemiological and laboratory study on scorpion stings in Khuzestan province. J. med. Facul. Guilan Univ. Med. Sci., 2: 5-12.

CHOUNG, R. S., JAFFE, H., CRIBBS, L., PEREZ-REYES, E. AND SWARTZ, K. J., 1998. Nature Neurosci., 1: 668.

CHOWELL, G., DIAZ-DUENAS, R., BUSTOS-SALDANA, A., MIRELES, A. AND FET, V., 2006. Epidimiological and clinical charecteristics of scorpionism in Colima, Mexico (2000-2001. Toxicology, 47: 753-758.

COELHO, F. M. AND PESSINI, A. M., 2007. Platlet activating factor receptors drive CXC chemokine producton, neutrophil influx and edema formation in the lungs of mice injected with Tityas serrulatus venom. Toxicon, 50: 420-427.

CORDEIRO, F. F., SAKATE, M. AND FERNANDES, V., 2006. Clinical and cardiovascular alterations produced by scorpion envenomation in dogs. J. Venom. Anim. Toxins. Trop. Dis., 12: 19-43.

CORNET, I., BUTTNER, K., DASSEUX, X. L. AND DUFOURCQ, J., 1994. The ampipathic alpha helix conceot. Application to the de novodesidg of ideally amphipathic Leu, Lys peptides with hemolytic activity higher than that of the mellitin. FEBS Lett., 349: 29.

CORRASA, M. M., SAMPAIO, S. V. AND LOPES, R. A., 1997. Biochemical and histopathological alterations induced in rats by Tityus serrulatus scorpion venom and its major neurotoxin tityustoxin-I. Toxicon, 35: 1053-1067.

DE SOUSA, A. R., DO NASCIMENTO, N. R. AND FERRERIRA-BARBOSA, D. M., 2005. Renal effects and vascular reactivity induced by Tityas serrulatus venom. Toxicon, 46: 271-276.

DEHGHANI, R., KHAMECHIAN, T., VATANDOOST, H., ASADI, M. A. AND MOSAVI, G. A., 2004. The effect of Hemiscorpius lepturus venom on pathologic changes of rat orangs. Q. Res. J. Lorestan Univ. Med. Sci. Hlth. Serv., 6: 37-41.

DEHGHANI, R., KHAMEHCHIAN, T., VAZIRIANZADEH, B., VATANDOOST, H. AND MORAVVEJ, S., 2012. Toxic effects of scorpion, hemiscorpius lepturus (hemiscorpiidae) venom on mice. J. Anim. Pl. Sci., 22: 593-596.

DESHPANDE, S. B., ALEX, A. B., JAGANNADHAM, M. V., RAO, G. R. AND TIWARI, A. K., 2005. Identification of novel pulmonary oedema producing toxin from Indian red scorpion (Mesobuthus tamulus) venom. Toxicon, 45:735-743.

EMAM, S. J., KHOSRAVI, A. D. AND ALEMOHAMMAD, A., 2008. Evaluation of haematological and urine parameters in Hemiscorpius lepturus (Gadim) victims referred to Razi Hospital, Ahwaz, Iran. J. med. Sci., 8: 306-309.

FARZANPEY, R., 1994. Scorpion sting and the fallowing of it. Pajouhesh va Sazandegi, 259: 123-125.

GOMEZ, A., BHATTACHARJEE, P., MISHRA, R., BISWAS, A.K., DASGUPTA, S.C. AND GIRI, B., 2010. Anticancer potential of animal venoms and toxins. Indian J. exp. Biol., 48: 93-103.

GORDON, D., ILAN, N., ZILBERBERG, N., GILLES, N., URBACH, D. AND COHEN, L., 2003. An 'Old World' scorpion beta-toxin that recognizes both insect and mammalian sodium channels. Eur. J. Biochem., 270: 2663-2670.

GUERON, M., MARGULIS, G. AND ILIA, R., 1993. The management of scorpion envenomation. Toxicon, 31: 1071-1083.

GWEE, M.C.E., NIRTTHANAN, S., KHOO, H., GOPALKRISHNAKONE, P., KINI, M.R. AND CHEAH, L.S., 2002. Autonomic effects of same scorpion venoms and toxins. Clin. exp. Pharmacol. Physiol., 29: 795-801.

HEEMSKERK, J. W., BEVERS, E. M. AND LINDHOUT, T., 2002. Platelet activation and blood coagulation. Thromb. Haemost., 88: 186-193.

ISMAIL, M. AND ABD-ELSALAM, A., 1998. Are the toxicological effects of scorpion envenomation related to tissue venom concentration Toxicon, 26: 256.

JALALI, A., VATANPOUR, H., HOSSEININASAB, Z., ROWANC, E. G. AND HARVEYC, A. L., 2007. The effect of the venom of the yellow Iranian scorpion Odontobuthus doriae on skeletal muscle preparations in vitro. Toxicon, 50: 1019-1026.

JALALI, A., BARVASAD-OMIDIAN, B., NAJAFZADEH, M. AND REZAEI, S., 2012. The pharmakokineticc of Hemiscorpius lepturus scorpion venom and Razi antivenom following intramuscular administration in rat. Venom Res., 3: 1-6.

KHARRAT, R., MANSUELLE, P., SAMPIERI, F., CREST, M., OUGHIDENI, R., RIETSCHOTEN, J. V., MARTIN-EAUCLAIRE, M. F., ROCHAT, H. AND AYUB, M. E., 1997. Maurotoxin, a four disulfide bridge toxin from Scorpio maurus venom: Purification, structure and action on potassium channels. FEBS Lett., 406: 284-290.

KLAASSEN, C. D. AND WATKINSIII, J. B., 2003. Casarett and Doull's essentials of toxicology. 3rd ed McGraw-Hill, New York, pp. 281-283.

LONGENECKER, G. L. AND LONGENECKER, H. E., 1981. Centruroides sculpturatus venom and platelet reactivity: possible role in scorpion venom induced defibrination syndrome. Toxicon, 19: 153-157.

MASIHIPOUR, B., 2005. Study about characterization of physic chemical and biological of Apitobuthus pterygo cercus venom of scorpion. Proc. Ist Iran. Congr. Biol. Sci., 822: 14-15.

MEBS, D., 2002. Scorpion and snakes such as Cobras, mambas and vipers made the African continent for venomous animals. Bull. Sci. Pathol. Exot., 95: 131.

MICHAEL, E. S. AND VICTOR, F., 2003. High-level systematics and phylogeny of the extant scorpions (Scorpiones: Orthosterni). Euscorpius, 11: 1-175.

MIRAKABADI, A.Z., JALALI, A., JAHROMI, A.E., VATANPUR, H. AND AKBARY, A., 2006. Biochemical changes and manifestations of envenomation produced by Odentobuthus doriae venom in rabbits. J. Venom. Anim. Toxins, Trop. Dis., 12:67-77

MURTHY, K. AND KRISHINA, R., 2002. On scorpion envenoming syndrome: Problems of medical ethics and accountability in medical research in India. J. Venom Anim. Toxins, 8: 10-13.

NUNAN, E. A., MORAES, M. F. D., CARDOSO, V. N. AND MORAES-SANTOS, T., 2003. Effect of age on body distribution of Tityustoxin from Tityus serrulatus scorpion venom in rats. Life Sci., 73: 319325.

NUNAN, E. A., ARYA, V., HOCHHAUS, G., CARDOSO, V. N. AND MORAES-SANTOS, T., 2004. Age effects on the pharmacokinetics of tityustoxin from Tityus serrulatus scorpion venom in rats, Brazil. Med. Biol. Res., 37: 385390.

OZKAN, O., CIFTCI, F. AND KARAER, Z., 2011. Electrophoretical comparison of proteins of Mesobuthus eupeus and Mesobuthus gibbosus scorpion venoms. Kafkas Aniv. Vet. FakA1/4l. Dergisi, 16: 153-158.

OZKAN, O. AND CARHAN, A., 2008. The nuteralizing capacity of Androctonus crassicauda antivenom against Mesobuthus eipeus scorpion venom. Toxicon, 52:375-397.

PETRICEVICH, V.L., 2010. Scorpion venom and inflammatory response. Med. Inflam., 2010: doi:10.1155/2010/903295

PINTO, M.C.L., MELO, M.M., COSTA, M.E.R. AND LABARRERE, C.R., 2010. Hematological and biochemical profiles of rats submitted to experimental poisoning with Tityus serrulatus venom. Arq. Brasil. Med. Vet. Zootec., 62: 2 Belo Horizonte. http://dx.doi.org/10.1590/S0102-09352010000200015.

PIPELZADEH, M. H., JALALI, A., TARAZ, M., POURABBAS, R. AND ZAREMIRAKABADI, A., 2007. An epidemiological and a clinical study on scorpionism by the Iranian scorpion Hemiscorpius lepturus. Toxicon, 50: 984-992.

POSSANI, L. D., MERINO, E., CORONA, M., BOLIVAR, F. AND BECERRIL, B., 2000. Peptides and genes coding for scorpion toxins that affect ion-channels. Biochimistery, 82: 861-868.

RATES, B., FERRAZ, K.K., BORGES, M.H., RICHARDSON, M., DE LIMA, M.E. AND PIMENTA, A.M., 2008. Tityus serrulatus venom peptidomics: assessing venom peptide diversity. Toxicon, 52: 611-618.

ROCHET, H., BARNARD, P. AND COURAUD, F., 1979. Scorpion toxin: Chemistry and mode of action. Adv. Cytopharmacol., 3: 325-334.

RODRIGUEZ, R.C. AND POSSANI, L.D., 2005. Overview of scorpion toxins specific for Na+ channels and related peptides: biodiversity, structure-function relationships and evolution. Toxicon, 46: 831844.

RUMING, Z., YIBAO, M., YAWEN, H., ZHIYONG, D., YINGLIANG, W., ZHIJIAN, C. AND WENXIN, L., 2010. Comparative venom gland transcriptome analysis of the scorpion Lychas mucronatus reveals interaspecific toxic gene diversity and new venomous components. BMC Genom., 11: 1-15.

SARAKAR, S., BHATTACHARYA, P. AND PASWAN, A., 2008. Cerebrovascular manifestations and alteration of coagulation profile in scorpion sting; a case series. Indian J. Crit. Care, 12: 15-17.

SCHWARTZ, E. F., DIEGO-GRACIA, E., RODRIGUEZ DE LA VEGA, R. C. AND POSSSNI, L. D., 2007 Tronscriptome analysis of venom gland of the Mexican scorpion Hadrurus gertschi (Arachnida: Scorpions). BMC Genom., 8: 119.

SEVERINO, D.N., PEREIRA, R. L., KNYSAK, I., CANDIDO, D.M. AND KWASNIEWSKI, F.H., 2009. Edematogenic activity of scorpion venoms from the Buthid family and role of platelet-activating factor and nitric oxide in new edema induced by Tityus venoms. Inflammation, 32: 57-64.

SHAHBAZZADEH, D., SRAIRI-ABID, N., FENG, W., RAM, N., BORCHANI, L., RONJAT, M., AKBARI, A., PESSAH, I.N., DE-WAARD, M. AND EL AYEB, M., 2007. Hamicalcin, a new toxin from the Iranian scorpion Hemiscorpius lepturus which is active on ryanodine-sensitive Ca2+ channels. Biochem. J., 404: 89-96.

SHIRMARDI, S. P., GANDOMKAR, M., SHAMSAEI, M., MIRAKABADI, A. Z., MARAGHEH, M. G., SHAFIEI, M. AND VAHIDFAR, N., 2010. Preparation and biodistribution study of a 99mTc-labeled toxic fraction of Iranian Mesobuthus eupeus scorpion venom. Iranian J. Nucl. Med., 18: 37-44.

SOFER, S. AND GUERON, M., 1990. Vasodilators and hypertensive encephalopathy following scorpion envenomation in children. Chest, 97: 118-20.

VATANPOUR, H., AHMADI, F., MIRAKABADI, A. Z. AND JALALI, A., 2012. Two biological active fractions isolated from Buthotus schach (BS) scorpion venom examined on striated muscle preparation, In-vitro. Iranian J. Phamacol. Res., 11: 905-911.

ZAYERZADEH, E., KOOHI, M. K., MIRAKABADI, Z. A., PURKABIREH, M. AND KASSAAIAN, S. E., 2010. Cardiopulmonary complications induced by Iranian Mesobuthus eupeus 53 scorpion venom in anesthetized rabbits. J. Venom Anim. Toxins. Trop. Dis., 16: 46-59.

ZLOTKIN, E., EITAN, M., BINDOKAS, V. P., ADAMS, E., MOYER, M., BURKHART, W. AND FOWLER, E., 2001. Functional duality and structural uniqueness of depressant insect-selective neurotoxins. Biochemistry, 30: 4814-4821.
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