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中药抗炎作用及其机制研究进展 总被引:2,自引:0,他引:2
20世纪后,人们对炎症的研究逐渐转移到了炎症发生、发展的机制和药物抗炎机制方面,从而开拓了一个十分重要的研究领域,为防治畜禽疾病提供了新的策略。目前。临床治疗中除肾上腺皮质激素类与非甾体类抗炎药物(NSAID)以外,部分中药也逐渐应用于抗炎。由于许多化学合成药物具有较强毒副反应,人们更加重视从天然药物中开发毒副作用较小的抗炎药物,用现代科学方法研究中药抗炎机制与临床应用是当今世界新药开发的热点。 相似文献
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解热镇痛抗炎药是一类具有抑制前列腺素合成而退高热、减轻局部钝痛,抗炎、抗风湿作用,因与甾体类糖皮质激素不同,故又称非甾体类抗炎药(NSAIDs).该类药物在临床应用较多,但由于种类较多,各有侧重且有不良反应,本文将对其分门别类进行介绍. 相似文献
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解热镇痛抗炎药是一类具有抑制前列腺素合成而退高热、减轻局部钝痛,抗炎、抗风湿作用,因与甾体类糖皮质激素不同,故又称非甾体类抗炎药(NSAIDs)。该类药物在临床应 相似文献
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选取贝尼尔(血虫净)、土霉素、盐酸四环素、新砷凡纳明(914)、咪唑苯脲、磺胺间甲氧嘧啶6种药物,进行猪附红细胞体的体内和体外对照治疗,结果 6种药物均有较好的疗效。猪附红细胞体病的治疗药物较多,临床上可以根据当地的流行情况灵活选用,其中盐酸四环素可以作为治疗猪附红细胞体病的首选药物。 相似文献
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犬椎间盘疾病概述 总被引:1,自引:0,他引:1
椎间盘疾病 (IVDD)主要是指椎间盘突出症 ,是因椎间盘变性、纤维环破裂 ,髓核向背侧突出压迫脊髓而引起的 ,以运动障碍为主要特征的脊椎疾病。目前 ,我国在人医方面对于 IVDD的研究较多 ,也较深入。而在兽医领域 ,对于 IVDD的认识还不是很深。本文旨在回顾国内外早期和近期的关于犬颈部和胸腰部 IVDD的病理生理学、诊断和治疗的文章 ,并且参考了一些人医相关方面的知识 ,以便日后对犬的IVDD做进一步的研究。1 发展历史关于犬的椎间盘疾病的报道早在 1881年就由Janson报道。 1896年 Dexler报道了犬由于椎间盘疾病造成的慢性压迫性… 相似文献
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产蛋鸡马杜霉素中毒的处理 总被引:1,自引:0,他引:1
1.联合用药后,治疗效果提高,不良反应减弱或消除,这种结果称为协同作用。如:(1)喹诺酮类和林可霉素同时使用能够起协同作用,特别适用于治疗鸡霉浆体病合并大肠杆菌病。(2)磺胺类药物和土霉素联合应用时,其结果相当于它们原有作用的相加。(3)磺胺类药物和TMP合用时,由于两种药物可分别阻断病原微生物叶酸合成代谢中前后两个不同环节,所以疗效能够增加数倍。2.联合用药后出现疗效减弱或消失,毒性增加等现象,这种情况就是配伍禁忌。(1)硫酸粘菌素和氨基糖苷类药物联用可导致神经系统中毒而产生肌无力和呼吸暂停的… 相似文献
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犬特应性皮炎是一种具有遗传倾向的过敏性皮肤病。由于近年来我国养犬数量不断增加,犬特应性皮炎成为宠物临床上的常见疾病,严重危害了宠物犬的身体健康。该病病因复杂,大致可概括为遗传因素、环境因素、皮肤屏障功能失调、免疫功能失调和微生物菌群失调五个方面,且由于其临床症状与其他过敏反应、炎症反应相似,难以确诊,需要通过多种临床反应共同判定。随着小动物诊疗的不断发展,犬特应性皮炎治疗在以往基础疗法上又增加了使用抗炎止痒药物、JAK通路抑制药物、生物制品药物和PED-4 选择性抑制剂等治疗方式。本文综述了近年来犬特应性皮炎的病因、临床症状、诊断方法和治疗方法方面的研究进展,以期为犬特应性皮炎的治疗提供借鉴和参考。 相似文献
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The treatment of canine atopic dermatitis is multifaceted and consists of a combination of actions that include the use of allergen avoidance, anti-inflammatory agents, allergen-specific immunotherapy and antimicrobial drugs. The importance and order of these treatment steps vary from patient to patient. General recommendations for each of the therapeutic steps are highlighted in this paper. Specific details are covered in other papers of this issue. 相似文献
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McMichael MA Ruaux CG Baltzer WI Kerwin SC Hosgood GL Steiner JM Williams DA 《American journal of veterinary research》2006,67(7):1226-1231
OBJECTIVE: To measure 15F(2t) isoprostane concentrations in the urine of dogs undergoing ovariohysterectomy (OHE) and dogs undergoing surgery because of intervertebral disk disease (IVDD) and to assess relationships between urinary concentrations of 15F(2t) isoprostanes and neurologic score in dogs with IVDD. ANIMALS: 11 dogs undergoing OHE and 32 dogs with IVDD undergoing hemilaminectomy. PROCEDURES: Paired urine samples were obtained at induction of anesthesia and approximately 1 hour after OHE (controls) and were collected from dogs with IVDD at induction of anesthesia (28 samples) and approximately 1 hour after hemilaminectomy (31 samples); 26 paired urine samples were obtained from dogs with IVDD. Urinary isoprostane concentrations were measured by use of a commercial ELISA, and results were adjusted on the basis of urinary creatinine concentrations. Differences in the mean isoprostane-to-creatinine ratio were analyzed. Neurologic score was determined in dogs with IVDD by use of the modified Frankel scoring system. RESULTS: Urinary isoprostane-to-creatinine ratios were significantly higher in dogs with IVDD than in control dogs before and after surgery. There was no significant difference between values before and after surgery for either group. There was a significant correlation of neurologic score and urinary isoprostane-to-creatinine ratio because dogs that had higher neurologic scores (ie, less severely affected) generally had higher isoprostane-to-creatinine ratios. CONCLUSIONS AND CLINICAL RELEVANCE: Urinary isoprostane-to-creatinine ratios were higher in dogs with IVDD before and after surgery. Analysis of these data suggests that dogs with IVDD are in a state of oxidative stress and that preemptive treatment with antioxidants warrants further investigation. 相似文献
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The pharmacotherapy of canine atopic dermatitis has relied primarily on the use of glucocorticoids and anti-histamines. During the last decade, other anti-inflammatory drugs have been investigated in clinical trials. This paper will review the studies using misoprostol, cyclosporine, tacrolimus, phosphodiesterase inhibitors, capsaicin, leukotriene inhibitors and serotonin-reuptake inhibitors for treatment of dogs with atopic dermatitis. For each drug the mechanism of action, the rationale for use in atopic dermatitis, the clinical efficacy, reported adverse effects and strength of recommendation for treatment of canine atopic dermatitis are described. At the time of this writing, there is fair evidence to support the recommendation for using cyclosporine, misoprostol and pentoxifylline for treatment of canine atopic dermatitis. This recommendation can be strengthened by the performance of additional blinded randomized controlled trials with larger number of dogs. In contrast, there is insufficient evidence to recommend for or against treatment with tacrolimus, leukotriene inhibitors, serotonin-reuptake antagonists and capsaicin. 相似文献
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Antihistamines frequently are recommended by veterinary dermatologists for symptomatic treatment of pruritus associated with canine atopic dermatitis (AD), perhaps because of their moderate success in some human patients with AD. A critical review of the literature describing antihistamine use in canine AD reveals that the majority of published, peer-reviewed studies are open, uncontrolled or partially-controlled trials. Such studies vary widely in reported efficacy, from perhaps 0 to 75% of patients, even using the same drug. The few blinded placebo-controlled trials available have failed to confirm efficacy of these drugs to relieve the pruritus of canine AD. Some studies indicate that synergistic effects could occur with concurrent use of essential fatty acid supplements. Consequently, at the time of this writing, there is insufficient evidence to conclude for or against the efficacy of antihistamines for treatment of canine AD. Additional blinded, randomized and controlled trials with larger numbers of patients are necessary to establish which of the antihistamine drugs currently available, if any, are truly efficacious for canine AD. Nevertheless, present clinician consensus suggests that several different antihistamine drugs should be evaluated in sequence, for 7-14 days each, in canine patients with AD. 相似文献
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Chandler K 《Veterinary journal (London, England : 1997)》2006,172(2):207-217
Epilepsy is a common neurological disorder in both dogs and humans. It is refractory to therapy in approximately one-third of canine patients, and even with the advent of new antiepileptic drugs for humans, appropriate treatment options in dogs remain limited. The pathogenesis and pathophysiology of epilepsy is being studied extensively in both human patients and rodent models of experimental epilepsy at the cellular and molecular level, but very little is known about the aetiologies of epilepsies in dogs. In this review, canine epilepsy will be discussed with reference to the human epilepsies and experimental epilepsy research. There is much work to be done in order to classify canine seizure types and breed-specific epileptic syndromes, particularly with reference to electroencephalographic abnormalities and possible genetic abnormalities. The review considers the appropriate use of antiepileptic drugs: phenobarbitone and potassium bromide are effective in most canine patients, although dosing regimes need to be carefully tailored to the individual, with serum concentration measurement. However, a significant proportion of patients remains refractory to these drugs. Work is currently underway to test the efficacy of newer antiepileptic drugs in the treatment of canine epilepsy, and preliminary data suggest that human drugs such as levetiracetam and gabapentin are of benefit in dogs with refractory epilepsy. 相似文献
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Pulmonary metastasis is a major cause of death and a major obstacle to the successful treatment of canine osteosarcoma. However, the residual capacity of the neoplasia for differentiation and its susceptibility to undergo apoptosis may be used to suppress its growth and metastatic properties. The highly metastasizing POS (HMPOS) canine osteosarcoma cell line which preferentially metastasize to the lungs was used to test the possible efficacy of 22-oxa-calcitriol (OCT) and all- trans retinoic acid (ATRA) to inhibit growth and pulmonary metastasis of the subcutaneously grown osteosarcoma in nude mice. Treatments in vitro, morphologically elongated and increased alkaline phosphatase activity and staining of cells. Tumour growth in vivo was inhibited significantly and the combination treatment of OCT and ATRA (OCT + ATRA) exerted a synergistic and stronger suppression at concentration of 1.0 microg kg(-1)body weight when given subcutaneously three times a week for 5 weeks. The subcutaneous tumours of the control mice consisted of osteoblast-like cells and isolated chondroblast-like cells, but formed several areas of osteoid and increased amount of collagen tissue in all treated mice. Pinpoint macrometastatic nodules developed only in all control mice. Micrometastatic nodule developed only in two of six mice treated with ATRA. However, nodule size and number, and lung wet weight were all reduced significantly. Metastasis were not seen in the mice treated with OCT or OCT + ATRA. This study demonstrated that inhibition of growth and pulmonary metastasis was induced by subcutaneous treatment with these drugs and suggest that both its differentiating and apoptotic inducing activities may be responsible for the antitumour effects. These drugs may be useful in the clinic as an adjunct for the treatment of canine osteosarcoma. 相似文献