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[目的]研究药用真菌灵芝、茯苓、红栓菌和扇菇菌运用双向固体发酵草乌后菌质(分别称为灵乌菌质、茯乌菌质、栓乌菌质和扇乌菌质)对小鼠的急性毒性作用和对大鼠心脏毒性的影响.[方法]运用双向发酵技术获得菌质,根据急性毒性预试验结果进行最大耐受量试验,采用Powerlab生理信号记录系统,通过观察大鼠Ⅱ导联心电图变化研究不同药物对大鼠的心脏毒性.[结果]相同剂量下灌胃给药,在给药7d后各处理组小鼠体重增长明显低于正常对照组;给药14 d后,灵乌菌质组体重增长很快,接近于正常对照组;与炮制品组相比,灵乌菌质组、扇乌菌质组和栓乌菌质组对大鼠心律失常发生次数有显著性降低作用(P <0.05或P<0.01),而茯乌菌质组对大鼠心律失常的影响和炮制品组没有显著差异;各发酵组间没有显著差异.[结论]灵乌菌质、扇乌菌质和栓乌菌质具有降低心律失常发生率的作用. 相似文献
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Severe hyperkalemia presenting with wide‐complex tachycardia in a puppy with acute kidney injury secondary to leptospirosis
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Andrew J. Brown MA VetMB DACVECC MRCVS Amy J. Alwood DVM Steven G. Cole DVM DACVECC 《Journal of Veterinary Emergency and Critical Care》2007,17(2):164-169
Objective: To describe a case of atrioventricular block and syncope secondary to systemic hypertension in a dog with malignant pheochromocytoma. Case Summary: A 13‐year‐old spayed female mixed‐breed dog presented following an acute onset of collapse. The dog was hypertensive and had paradoxical high‐grade second‐degree atrioventricular block with concurrent syncope. Initial emergent therapy included a nitroprusside infusion for the systemic hypertension and vagolytic therapy for the bradyarrhythmia. A left adrenal mass was seen on abdominal ultrasound and was further characterized by MRI. Following medical stabilization with phenoxybenzamine and propantheline, a left adrenalectomy was performed. Histological diagnosis was consistent with a malignant pheochromocytoma. Following tumor removal there has been no further hypertension, atrioventricular block or syncope. Unique information provided: This is the first documented case of a malignant pheochromocytoma presenting as syncope secondary to hypertension induced atrioventricular block. 相似文献
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HistoryA 2-year-old, entire female, Somali cat weighing 3.8 kg was admitted for a conjunctival graft on the right eye, for treatment of an acute descemetocele. Medetomidine 4.2 μg kg?1 and methadone 0.2 mg kg?1 were administered by intramuscular injection as preanaesthetic medication. Anaesthesia was induced using diazepam 0.26 mg kg?1 and propofol 4 mg kg?1 administered by intravenous (IV) injection. Following endotracheal intubation, anaesthesia was maintained with isoflurane delivered in oxygen (1 L minute?1) and nitrous oxide (2 L minute?1) via a non-rebreathing system. Twenty minutes after induction of anaesthesia, one drop of a 10% phenylephrine hydrochloride solution was administered topically to the right eye.Physical examinationAfter phenylephrine administration, a decrease in heart rate (from 95 to 80 beats minute?1) and an increase in arterial blood pressure occurred. The pulse then became difficult to palpate manually and multifocal ventricular premature contractions were observed on the electrocardiogram.ManagementNitrous oxide was discontinued and the isoflurane vaporizer setting was decreased from 1.5% to 0.5%. Lidocaine 1 mg kg?1 IV was administered, this resulted in ventricular bigeminy. The quality of the femoral pulse improved and was regular in rhythm and character. Surgery was completed as fast as possible. The bigeminy progressively disappeared and before disconnecting the cat from the breathing system, there was a normal sinus rhythm with a heart rate of 85 beats minute?1.Follow-upEchocardiography was performed during recovery and showed mitral and aortic valve insufficiency and dilation of the left ventricle, suggesting a reduction in systolic function. Echocardiography was repeated the following day and was normal.ConclusionsIn order to diminish the potential for cardiovascular sequelae associated with systemic absorption of ocular phenylephrine, less concentrated solutions, smaller drop size or different instillation techniques should be considered for topical use in small patients. 相似文献
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用氯化钙致家兔实验性心律失常和大鼠心肌缺血再灌注心律失常模型,观察噻苯唑的抗心律失常作用。结果表明:噻苯唑有较好的抗心律失常作用,其机理可能与对Ca^2+转运的影响有关。 相似文献
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Karen R. Humm MA VetMB DACVECC MRCVS ; Elizabeth A. Keenaghan-Clark MA VetMB MRCVS Amanda K. Boag MA VetMB DACVIM DACVECC FHEA MRCVS 《Journal of Veterinary Emergency and Critical Care》2009,19(4):352-356
Objective – To quantify the frequency of adverse events occurring during or post pericardiocentesis and to determine if adverse events are related to the cause of the pericardial effusion or frequency of pericardiocentesis.
Design – Retrospective study.
Setting – Referral hospital.
Animals, Intervention and Measurements – Medical records of 85 dogs that underwent 112 episodes of pericardiocentesis were reviewed. Any adverse events during pericardiocentesis and in the 48 hours post pericardiocentesis were noted. The frequency of adverse events was compared between dogs with a suspected neoplastic cause and a suspected nonneoplastic cause of their pericardial effusion and also between the first and subsequent pericardiocenteses.
Main Results – The incidence of adverse events was 10.7% within 1 hour of pericardiocentesis and 15.2% within 48 hours. There was no significant difference in the frequency of adverse events between the groups. Most adverse events identified were dysrhythmias. Forty-one percent of those dogs with adverse events were euthanized or died within 48 hours.
Conclusion – The incidence of adverse events seen within 48 hours of pericardiocentesis was 15.2%. 相似文献
Design – Retrospective study.
Setting – Referral hospital.
Animals, Intervention and Measurements – Medical records of 85 dogs that underwent 112 episodes of pericardiocentesis were reviewed. Any adverse events during pericardiocentesis and in the 48 hours post pericardiocentesis were noted. The frequency of adverse events was compared between dogs with a suspected neoplastic cause and a suspected nonneoplastic cause of their pericardial effusion and also between the first and subsequent pericardiocenteses.
Main Results – The incidence of adverse events was 10.7% within 1 hour of pericardiocentesis and 15.2% within 48 hours. There was no significant difference in the frequency of adverse events between the groups. Most adverse events identified were dysrhythmias. Forty-one percent of those dogs with adverse events were euthanized or died within 48 hours.
Conclusion – The incidence of adverse events seen within 48 hours of pericardiocentesis was 15.2%. 相似文献
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