12 results on '"PHYSIOLOGICAL effects of venom"'
Search Results
2. Severe Hemorrhagic Syndrome After Lonomia Caterpillar Envenomation in the Western Brazilian Amazon: How Many More Cases Are There?
- Author
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Santos, João Hugo A., Oliveira, Sâmella S., Alves, Eliane C., Mendonça-da-Silva, Iran, Sachett, Jacqueline A.G., Tavares, Antonio, Ferreira, Luiz Carlos, Fan, Hui Wen, Lacerda, Marcus V.G., and Monteiro, Wuelton M.
- Subjects
CATERPILLARS ,HEMORRHAGE ,PHYSIOLOGICAL effects of venom ,ANTIVENINS ,ANIMALS ,BITES & stings ,INSECTS ,MOTHS ,SYNDROMES ,THERAPEUTICS - Abstract
Contact with Lonomia caterpillars can cause a hemorrhagic syndrome. In Brazil, Lonomia obliqua and Lonomia achelous are known to cause this venom-induced disease. In the Brazilian Amazon, descriptions of this kind of envenomation are scarce. Herein, we report a severe hemorrhagic syndrome caused by Lonomia envenomation in the Amazonas state, Western Brazilian Amazon. The patient showed signs of hemorrhage lasting 8 days and required Lonomia antivenom administration, which resulted in resolution of hemorrhagic syndrome. Thus, availability of Lonomia antivenom as well as early antivenom therapy administration should be addressed across remote areas in the Amazon. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
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3. Lymphangitis From Scolopendra heros Envenomation: The Texas Redheaded Centipede.
- Author
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Essler, Shannon E., Julakanti, Maneesha, and Juergens, Andrew L.
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LYMPHATIC abnormalities ,SKIN inflammation ,PHYSIOLOGICAL effects of venom ,SCOLOPENDRA ,CENTIPEDES ,PATIENTS ,ANIMALS ,ARTHROPODA ,BITES & stings ,LYMPHATIC diseases - Abstract
Envenomation by Scolopendra heros, the Texas redheaded centipede, can present variably. Although transient pain and erythema are often treated conservatively, complications may include cellulitis, necrosis, myocardial infarction, and rhabdomyolysis. We present a case of an elderly man who came to the emergency department with lymphangitis and dermatitis secondary to a centipede sting that awoke him from sleep. It is important to recognize the potential of centipede envenomation to have severe local and systemic manifestations. [ABSTRACT FROM AUTHOR]
- Published
- 2017
- Full Text
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4. Two Successive Necrotic Lesions Secondary to Presumed Loxosceles Envenomation.
- Author
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Tarullo, David B., Jacobsen, Ryan C., and Algren, D. Adam
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BROWN recluse spider ,PHYSIOLOGICAL effects of venom ,SKIN injuries ,POISONOUS arachnida ,LOXOSCELES ,LOXOSCELIDAE - Abstract
Brown recluse spider (Loxosceles reclusa) envenomations with subsequent necrotic skin lesions occur infrequently, and systemic loxoscelism is rarer still. We report a case of 2 successive developing necrotic lesions, each on adjacent medial aspects of the legs, secondary to presumed Loxosceles envenomation. A 31-year-old man with no significant past medical history presented to the emergency department with 2, large, necrotic lesions, 1 on each medial thigh. They had progressed over the course of 1 month from small blisters to large necrotic lesions with eschar. He underwent surgical debridement without skin grafting with no further complications. Bites from recluse spiders that progress to necrosis usually present as single lesions. The differential diagnoses for a necrotic skin lesion is large. The presence of more than 1 lesion argues against Loxosceles envenomation; however, in the absence of underlying infection, systemic diseases, immunodeficiency, or malignancy, the diagnosis must be considered if the case presents in an endemic area. Brown recluse spiders rarely bite multiple times, thus confounding the diagnosis of an already nonspecific clinical finding. [ABSTRACT FROM AUTHOR]
- Published
- 2013
- Full Text
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5. Role of hyaluronidase inhibitors in the neutralization of toxicity of Egyptian horned viper Cerastes cerastes venom.
- Author
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Wahby, A.F., Mahdy, El-Sayed M.E., EL-mezayen, Hatem A., Salama, Walaa H., Ebrahim, Nihal M., Abdel-Aty, Azza M., and Fahmy, Afaf S.
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HYALURONIDASES ,ENZYME inhibitors ,NEUTRALIZATION (Chemistry) ,SNAKE venom ,PHYSIOLOGICAL effects of venom ,VIPERIDAE ,MEDICINAL plants ,SNAKEBITE treatment - Abstract
Abstract: Hyaluronidase “venom spreading factor” is a common component of snake venoms and indirectly potentiates venom toxicity. It may cause permanent local tissue destruction at the bite site/systemic collapse of the envenomated victim. The present study was performed to assess the benefits of inhibiting the hyaluronidase activity of Egyptian horned viper, Cerastes cerastes (Cc). The aqueous extracts of some medicinal plants were screened for their inhibitory effect on hyaluronidase activity of Cc venom. The results revealed that the Rosmarinus officinalis (Ro) extract is the most potent hyaluronidase inhibitor among the tested extracts. The Ro extract is more potent inhibitory effect on the hyaluronidase activity than the prepared rabbit monoclonal antiserum of previously purified hyaluronidase enzyme from Cc venom (anti-CcHaseII). In addition, the Ro extract is efficiently inhibited the activity of hemorrhagic toxin previously purified from Cc venom, and it also neutralized the edema inducing activity of the Cc venom in vivo. Furthermore, the Ro extract markedly increased the survival time of experimental mice injected with lethal dose of Cc venom up to 7h in compared to mice injected with venom alone or with venom/anti-CcHaseII (15±5, 75±4min), respectively. Our findings imply the significance of plant-derived hyaluronidase inhibitor in the neutralization of local effects of Cc venom and retardation of death time. Therefore, it may use as a therapeutic value in complementary snakebite therapy. [Copyright &y& Elsevier]
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- 2012
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6. EMERGENCIA HIPERTENSIVA EN EMPONZOÑAMIENTO ESCORPIÓNICO PEDIÁTRICO. REPORTE DE UN CASO.
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Ramirez Sanchez, Manuel S., Katida E.6Perez, Brena, Nelys, and Fuentes, Juvirma Pacheco
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SCORPION venom ,PHYSIOLOGICAL effects of venom ,ANTIVENINS ,DISEASES in girls - Abstract
Copyright of Archivos Venezolanos de Puericultura y Pediatría is the property of Sociedad Venezolana de Puericultura y Pediatria and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
- Published
- 2010
7. Some biological effects of scorpion envenomation in late pregnant rats.
- Author
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Ben Nasr, Hmed, Serria, Hammami, Chaker, Selma, Riadh, Badraoui, Zouheir, Sahnoun, Kamel, Jamoussi, Tarek, Rebai, and Khaled, Zeghal
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SCORPION venom ,PHYSIOLOGICAL effects of venom ,BLOOD pressure measurement ,PREGNANCY complications ,HEMODYNAMICS ,FETUS ,PREGNANCY in animals ,LABORATORY rats - Abstract
Abstract: Scorpion envenoming is less studied during gestation; however, it may induce various biological disturbances in maternal organism and hypothetical ones on their fetuses. The scope of this report was to elucidate some biological effects of such poisoning in late pregnant rats. Hence, TBARS levels in maternal lung, placental and fetal pulmonary and hepatic tissues and dam''s biochemical blood parameters (glucose, creatinine, 17-β estradiol, progesterone, blood nitrogen urea, sodium and potassium maternal plasma concentrations) had been evaluated after saline (G1), and scorpion venom (G2: 30min and G3: 60min) injections in 22nd day pregnant rats. Histological microscopic examination of these tissues was also carried out in HE-stained paraffin sections. In addition, the mean arterial blood pressure following the envenomation variations was measured in three rats from the same pool. Our results showed that Buthus occitanus tunetanus crude venom induced significant increase in maternal, placental and fetal tissues lipid peroxidation, concomitant with blood pressure elevation. Maternal plasma creatinine, estradiol and progesterone concentrations levelled up significantly after 30min or later (60min) after the venom injection. Except for a probable pronounced oedema and few congestions in maternal lungs and degenerative aspects of trophoblast cells, all examined tissues showed a conserved structure. These results suggest that scorpion envenomation may induce gestation process disturbances and threatens both mother''s and fetus’ well-being. [Copyright &y& Elsevier]
- Published
- 2009
- Full Text
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8. Sol i 1, the phospholipase allergen of imported fire ant venom.
- Author
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Hoffman, Donald R., Sakell, Rhonda H., and Schmidt, Margit
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PHOSPHOLIPASES ,FIRE ant venom ,INSECT allergy ,PHYSIOLOGICAL effects of venom ,CROSS reactions (Immunology) ,BEE venom ,IMMUNOGLOBULIN E ,PROTEOLYTIC enzymes - Abstract
Background: Sol i 1, the venom phospholipase of imported fire ant venom is an important allergen and exhibits some cross-reactivity with IgE antibodies from patients sensitized to other Hymenoptera venoms. Objective: To determine the primary structure of Sol i 1 and evaluate the roles of protein and carbohydrate epitopes in its cross-reactivity. Methods: Sol i 1 was purified from venom, proteolytic peptides prepared and amino acid sequences obtained. The cDNA for Sol i 1 was cloned, sequenced, and compared with sequences of other wasp venom phospholipases. The role of carbohydrate epitopes in the cross-reactivity with other Hymenoptera venoms was studied by RAST inhibition. Results: The sequence identified Sol i 1 as a lipase of the GX class, lipoprotein lipase superfamily, pancreatic lipase homologous family and RP2 subgroup phospholipases as are the vespid venom phospholipases. The 148 residues identified by amino acid sequencing represent about 48% of the translated cDNA sequence. Sol i 1 was 31-32% identical to yellow jacket phospholipases. The identical regions of sequence were clustered in the domain which forms the serine hydrolase active site. Mannosylated N-glycans could completely inhibit binding of IgE from honeybee venom sensitized patients to Sol i 1. Inhibition by glycan of IgE binding from yellow jacket venom sensitized patients was low or absent for three of eight sera and substantial, but not complete for five sera. Conclusions: Sol i 1 is related to wasp venom phospholipases. Cross-reactivity with honeybee venom is caused by carbohydrate, whereas cross-reactivity with yellow jacket venom involves reactivity with both carbohydrate determinants of hyaluronidase and high molecular weight proteins and phospholipase protein determinants. [ABSTRACT FROM AUTHOR]
- Published
- 2005
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9. Use of β-blockers during immunotherapy for Hymenoptera venom allergy.
- Author
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Müller, Ulrich R. and Haeberli, Gabrielle
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ADRENERGIC beta blockers ,IMMUNOTHERAPY ,INSECT venom ,PHYSIOLOGICAL effects of venom ,INSECT allergy ,HYMENOPTERA ,THERAPEUTIC complications ,CORONARY heart disease risk factors ,ALLERGY treatment - Abstract
Background: B-Blockers may aggravate anaphylactic reactions and interfere with treatment. There is therefore concern about their use in patients who have a history of anaphylaxis or are on allergen immunotherapy. Immunotherapy is the best available treatment for prevention of life-threatening anaphylaxis to Hymenoptera stings, which is often observed in elderly patients who have cardiovascular disease and therefore are on β-blocker treatment. Objective: To analyze the risk of β-blocker treatment during venom immunotherapy. Methods: We screened all 1682 patients with Hymenoptera venom allergy seen during a period of 34 months for immunotherapy, cardiovascular disease, and treatment with β-blockers. Results: Of the 1389 patients in whom immunotherapy was recommended, 11.2% had cardiovascular disease, and 44 of these were on β-blockers before immunotherapy. In 31 of those, the drug was replaced before starting treatment. In 3 with coronary heart disease and 1 with severe ventricular arrhythmia, the drug was continued throughout immunotherapy. In 9, it was reintroduced after reaching the maintenance dose. In an additional 12 patients, β-blockers were newly started during immunotherapy. Of 25 patients on β-blockers during immunotherapy, 3 (12%) developed allergic side effects, compared with 23 (16.7%) of 117 with cardiovascular disease but without β-blockers. Systemic allergic symptoms after re-exposure by sting challenge or field sting were observed in 1 of 7 (14.3%) with and 4 of 29 (13.8%) without β-blockade. No severe reactions to treatment or sting reexposure were observed in patients with β-blockade. Conclusion: Combination of β-blockers with venom immunotherapy may be indicated in heavily exposed patients with severe cardiovascular disease. [ABSTRACT FROM AUTHOR]
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- 2005
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10. ALLERGY & ASTHMA: J. Thaddaeus Abbott, M.D.
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ALLERGISTS ,ASTHMATICS ,ALLERGY treatment ,PHYSIOLOGICAL effects of venom ,HUMAN services - Abstract
The article profiles allergist Thaddaeus Abbott, who committed himself in helping people suffering asthma and allergies. Topics discussed include his work as a medical specialist at the University of Utah, the treatment plans being provided by Abbott that improves his patient's life, and his advanced training that enables him to create treatments for venom allergies.
- Published
- 2015
11. Gartersnakes.
- Author
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Mui, Jen
- Subjects
GARTER snakes ,PHYSIOLOGICAL effects of venom ,VENOM resistance ,SNAKE venom ,CROTOXIN - Abstract
The article offers information on gartersnakes. Gartersnakes have 16 species in North America in which four can be found in Illinois including the Plains and Common gartersnakes and the Western and Eastern Ribbonsnakes. The author shares that although technically poisonous, gartersnakes do not pose a large threat to humans because they can not store large amounts of poison. Information on the snake's habitat is also presented.
- Published
- 2014
12. Paging Doc Oc.
- Subjects
PHYSIOLOGICAL effects of venom ,DRUG development ,MEDICAL research - Abstract
The article discusses a research by Bryan Fry and colleagues which investigated whether the venom found in octopuses, cuttlefish and some squid contain compounds that can help develop drugs for conditions like pain management, allergies and cancer.
- Published
- 2009
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