Effect of acid secretion blockade on acute gastric mucosal lesions induced by Tityus serrulatus scorpion toxin in anaesthetized rats

Scorpion venom (TX) promotes gastric acid and pepsin secretion leading to acute gastric mucosal lesions (AGML), when injected in animals. The goal of the present study was to observe the effects of acid gastric secretion blockers over the incidence of TX-induced AGML in vivo. To verify this model, w...

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Veröffentlicht in:Toxicon (Oxford) 2006-10, Vol.48 (5), p.543-549
Hauptverfasser: Melo, Júnio Rios, de Araújo, Gnana Keith Marques, da Luz, Magda Maria Profeta, da Conceição, Sérgio Alexandre, Lisboa, Felipe Assis, Moraes-Santos, Tasso, Cunha-Melo, José Renan
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container_end_page 549
container_issue 5
container_start_page 543
container_title Toxicon (Oxford)
container_volume 48
creator Melo, Júnio Rios
de Araújo, Gnana Keith Marques
da Luz, Magda Maria Profeta
da Conceição, Sérgio Alexandre
Lisboa, Felipe Assis
Moraes-Santos, Tasso
Cunha-Melo, José Renan
description Scorpion venom (TX) promotes gastric acid and pepsin secretion leading to acute gastric mucosal lesions (AGML), when injected in animals. The goal of the present study was to observe the effects of acid gastric secretion blockers over the incidence of TX-induced AGML in vivo. To verify this model, we used male albino rats, fasted 18–20 h ( n = 122 ) and anaesthetized with urethane (1.4 g/kg, i.p.). Their trachea and left femoral vein were both cannulated; the first to avoid airway obstructions during scorpion intoxication and the second for administration of saline, TX and acid blockers. Following the surgical procedure, the animals were divided in 10 groups of at least 10 animals each. Control groups were injected with NaCl 0.9% 1 ml/kg ( n = 10 ) or TX 375 μg/kg ( n = 32 ). Test groups ( n = 10 , each) received atropine 5 mg/kg, cimetidine 10 mg/kg, ranitidine 2.5 mg/kg, ranitidine 5 mg/kg, omeprazol 1 mg/kg, omeprazol 4 mg/kg, octreotide 80 and octreotide 100 μg/kg 10 min before the TX was injected. After 1 h of intoxication, the stomach was resected for macroscopic study and the gastric secretion was collected for volume, pH and acid output assessment. We observed that all blockers were able to completely or partially prevent the TX-induced acid secretion as well as the AGML ( p < 0.05 ). Our data suggest the TX-induced AGML can be prevented by different class of acid blockers injected before the intoxication.
doi_str_mv 10.1016/j.toxicon.2006.07.003
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After 1 h of intoxication, the stomach was resected for macroscopic study and the gastric secretion was collected for volume, pH and acid output assessment. We observed that all blockers were able to completely or partially prevent the TX-induced acid secretion as well as the AGML ( p &lt; 0.05 ). Our data suggest the TX-induced AGML can be prevented by different class of acid blockers injected before the intoxication.</abstract><cop>Oxford</cop><pub>Elsevier Ltd</pub><pmid>16926041</pmid><doi>10.1016/j.toxicon.2006.07.003</doi><tpages>7</tpages></addata></record>
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source MEDLINE; ScienceDirect Journals (5 years ago - present)
subjects Acid secretion blockers
Acute Disease
Acute gastric mucosal lesions
Anesthesia
Animal poisons toxicology. Antivenoms
Animals
Atropine - pharmacology
Biological and medical sciences
Cimetidine - pharmacology
Dose-Response Relationship, Drug
Drug Antagonism
Enzyme Inhibitors - pharmacology
Gastric Acid - secretion
Gastric Mucosa - drug effects
Gastric Mucosa - pathology
Gastric Mucosa - secretion
Gastric secretion
Gastrointestinal Agents - pharmacology
Male
Medical sciences
Neurotoxins - analysis
Neurotoxins - toxicity
Octreotide - pharmacology
Omeprazole - pharmacology
Pepsin A - secretion
Ranitidine - pharmacology
Rats
Scorpion toxin
Scorpion Venoms - analysis
Scorpion Venoms - toxicity
Stomach Diseases - chemically induced
Stomach Diseases - pathology
Stomach Diseases - prevention & control
Tityus serrulatus
Toxicology
title Effect of acid secretion blockade on acute gastric mucosal lesions induced by Tityus serrulatus scorpion toxin in anaesthetized rats
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