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1.
复合剂组方研究和健康犬麻醉实验结果表明,选用神经安定、高效镇痛和肌肉松弛作用药物试制成的动物全身麻醉复合剂—846注射液,对小鼠、大鼠和实验犬有较理想的镇痛、镇静和肌肉松弛作用,具有给  相似文献   

2.
比格犬是国际通用的标准化实验用犬,目前对其麻醉方案仍不够完善,无法满足日益多样化的麻醉需要。本文从麻醉方式、临床应用、抗炎作用及不良反应等几个方面,总结兽医临床利用丙泊酚对犬进行注射麻醉的研究进展及应用效果,为实验过程中制定比格犬的麻醉方案提供参考。  相似文献   

3.
将20条杂种家犬随机分为4组进行临床麻醉实验,即静松灵组(A)、氯胺酮组(B)、静松灵与氯胺酮复合麻醉组(C)和846合剂组(D),分别检测犬在麻醉前、麻醉后30 m in、4 h、24 h、48 h 5个时点血清中天门冬酸氨基转移酶、丙氨酸氨基转移酶、尿素氮、肌酐的含量并进行分析比较。结论:C组、D组进行复合麻醉时比A组、B组单纯麻醉时对犬肝、肾功能影响小,说明对犬进行复合麻醉比单纯麻醉更为安全。  相似文献   

4.
犬的断尾方法   总被引:1,自引:0,他引:1  
1犬的断尾术式 1.1犬的保定与麻醉犬的尾部有较大的神经、血管分布,行断尾术前须作局部浸润麻醉,体型较大、性情凶猛的犬应进行全麻。全麻常用2%“静松灵”,按0.1—0.2mL/kg,或“846”复合麻醉剂,按0.01mL/kg,皮下或肌肉注射,局部麻醉一般用盐酸普鲁卡因,剂量视犬体大小而定。麻醉后固定好犬的四肢,作侧卧保定。  相似文献   

5.
通过采用异氟烷对犬进行吸入麻醉和麻醉监测,探讨异氟烷对犬合理的吸入麻醉方式以便进行复杂的外科手术。在以注射丙泊酚3 mg/kg体重进行诱导麻醉的条件下,通过选取异氟烷为1%,1.5%,2%,2.5%,3%,4%6个浓度点对8只实验犬进行吸入麻醉,并进行麻醉监测,结果显示:随着异氟烷浓度增加,犬的呼吸次数逐渐降低,心率减慢,血氧饱和度下降。浓度为4%时,8只犬血氧饱和度均低于85%,缺氧严重;浓度为2.5%~3%时,麻醉迅速但持续时间不宜过长,当浓度为1%~2%时,进入麻醉状态慢,但对犬心脏和肺抑制作用小。  相似文献   

6.
犬QFM麻醉的综合监测   总被引:3,自引:0,他引:3  
QFM是一种自行研制的新型犬用复合麻醉制剂。为了验证QFM的麻醉效果及对生理功能的影响,以0.15~0.2mL/kg剂量对7只犬进行麻醉,进行了单纯麻醉监测和QFM麻醉监测期间手术验证试验。结果证明:QFM无论单纯进行犬的麻醉,还是在麻醉过程中进行手术处置,都具有较为确实的麻醉效果,且镇静、镇痛、肌松效果均衡,诱导及复苏迅速平稳,无流涎和呕吐等负反应发生,对机体的正常生理功能及各项生理指标影响轻微,血氧饱合始终维持在90%以上,可为犬的临床常规手术提供良好的手术条件。但手术刺激对其药理作用有轻微的拮抗作用。  相似文献   

7.
比格犬是国际通用的标准化实验用犬,在药理学、毒理学、外科学、微生物学等多个领域有广泛的应用.论文综述了比格犬麻醉技术的研究进展,包括吸入麻醉、注射麻醉、复合麻醉以及麻醉前给药等,以期为科研人员开展比格犬相关麻醉操作提供参考.  相似文献   

8.
为了观察犬眠宝注射麻醉和异氟醚吸入麻醉对经历去势术犬血浆中甲状腺激素T3、T4的影响,试验将20只实验犬随机均分为犬眠宝注射麻醉组(Q组)和异氟醚吸入麻醉组(I组),每组10只。两组分别进行犬去势术,术中进行麻醉监测,并采静脉血,用放射性免疫法(RIA),检测血浆的含量,测定血浆中的T3、T4。试验结果表明,犬眠宝、异氟醚麻醉及手术对犬血浆中T3、T4的影响具有相似之处,均表现为术中升高,术后持续降低直至48h恢复到麻醉前水平。  相似文献   

9.
噻胺酮是一种以氯胺酮和二甲苯胺噻嗪为主的新型复合麻醉剂,除对犬、猫有良好的制动和麻醉作用外,对小型猪的麻醉效果也甚为理想,本实验采用动物给药前后自  相似文献   

10.
应用8条犬通过自身循环对照试验,观察了犬醒宝、苯噁唑对犬眠宝麻醉犬的催醒作用。结果显示,犬醒宝在肌肉注射犬眠宝0.02 mL/kg体重后20 min肌肉注射0.02 mL/kg体重进行复苏,平均唤醒时间为1.6 min±0.7min,平均自主站立行走时间为3.1 min±1.2 min;肌肉注射犬眠宝0.02 mL/kg体重麻醉后应用1%苯噁唑0.04 mL/kg体重进行复苏,平均唤醒时间为6.6 min±2.1 min,平均自主站立行走时间为8.3 min±1.9 min。犬醒宝复苏组与1%苯噁唑复苏组比较,催醒效果差异极显著(P<0.01),且犬醒宝应用于犬眠宝的复苏具有用量小,复苏迅速安全,无复睡现象,可用于犬眠宝的临床麻醉复苏。  相似文献   

11.
Medical records of 151 dogs with chronic hepatitis were reviewed. Corticosteroid treatment had a statistically significant (P less than 0.005) effect on improving survival time when corticosteroid-treated dogs were compared with untreated dogs. Dogs dying within 1 week of examination represented 37.1% of the cases, and when compared with those living more than 1 week, serum glucose concentration was significantly lower (P less than 0.001); prothrombin time and partial thromboplastin time were significantly longer (P less than 0.001); blood ammonia concentration after oral administration of ammonium chloride was significantly higher (P less than 0.05); and necrosis severity and fibrosis severity were significantly greater (P less than 0.05 and P less than 0.022, respectively). The best predictors of early death were low normal serum glucose concentration (P less than 0.001) and prolonged prothrombin time (P less than 0.030), which was abnormal in 60.0% of dogs dying early. Partial thromboplastin time, which was increased in 92.0% of dogs dying early and in 42.6% of dogs living more than 1 week, was a less reliable predictor. Plasma ammonia concentration after oral administration of NH4Cl was least reliable in predicting early death. In dogs living more than 1 week, hypoalbuminemia was a predictor of shorter survival time (P less than 0.003). Of all the histologic features evaluated, only necrosis severity and fibrosis severity were accurate predictors of early death. The presence of bridging fibrosis was a predictor of shorter survival time in dogs living more than 1 week (P less than 0.0002).  相似文献   

12.
Serum concentrations of thyrotropin (TSH), prolactin, thyroxine, and 3,5,3'-triiodothyronine in 15 euthyroid dogs and 5 thyroidectomized and propylthiouracil-treated dogs after thyrotropin-releasing hormone (TRH) administration were measured. Although thyroidectomized and propylthiouracil-treated dogs had higher (P less than 0.01) base-line concentrations of TSH in serum than did euthyroid dogs, concentrations of TSH after TRH administration varied at 7.5, 15, and 30 minutes with 14 of 45 samples obtained from healthy dogs having lower TSH concentrations than before TRH challenge. Similarly, concentrations of 3,5,3'-triiodothyronine in the serum of euthyroid dogs 4 hours after TRH administration were similar (P less than 0.05) to concentrations before TRH challenge. Although the mean concentration of thyroxine in serum was elevated (P less than 0.05) 4 hours after administration of TRH to euthyroid animals, as compared with base-line levels, the individual response was variable with concentrations not changing or decreasing in 4 dogs. Therefore, the TRH challenge test as performed in the current investigation was of limited value in evaluating canine pituitary gland function. Although mean concentrations of TSH in serum were higher (P less than 0.05) in euthyroid dogs after TRH administration, the response was too variable among individual animals for accurate evaluation of pituitary gland function. Concentrations of prolactin in the sera of dogs after TRH administration, confirmed previous reports that exogenously administered TRH results in prolactin release from the canine pituitary and indicated that the TRH used was biologically potent.  相似文献   

13.
Ten dogs were given mitoxantrone at a dose of 5 mg/m2 body surface area intravenously. Recombinant canine granulocyte colony-stimulating factor (rcG-CSF) was administered subcutaneously daily for 20 days after an infusion of mitoxantrone in five of these dogs to determine the effect of the hematopoietic growth factor on the duration and severity of myelosuppression. The median neutrophil counts dropped below normal (less than 3,000/uL) for 2 days in the dogs that received rcG-CSF, and for 5 days in the dogs that received only mitoxantrone. Four of five dogs not treated with rcG-CSF and none of those receiving rcG-CSF developed serious neutropenia (less than 1,500/uL). The neutrophil counts were significantly (P less than 0.05) higher in the rcG-CSF treated dogs at all time points except before the administration of the colony-stimulating factor, and the sixth day after the mitoxantrone was administered. These findings demonstrate that rcG-CSF is capable of reducing the duration and severity of mitoxantrone-induced myelosuppression.  相似文献   

14.
Two low-dose dexamethasone suppression test protocols were evaluated in 18 dogs with hyperadrenocorticism (14 dogs with pituitary-dependent hyperadrenocorticism [PDH] and 4 dogs with adrenocortical tumor) and in 5 healthy control dogs. Blood was obtained immediately before and 2, 4, 6, and 8 hours after IV administration of either 0.01 mg of dexamethasone sodium phosphate/kg of body weight or 0.015 mg of dexamethasone polyethylene glycol/kg. At 8 hours after dexamethasone administration, 18 of 18 (100%) dogs with hyperadrenocorticism given the sodium phosphate preparation and 16 of 18 (89%) affected dogs given the polyethylene glycol preparation failed to have suppression of plasma cortisol concentration (less than 1.4 micrograms/dl). Plasma cortisol concentration was suppressed to less than 1.4 micrograms/dl at 2, 4, and/or 6 hours after administration of either dexamethasone preparation in 5 of 14 dogs with PDH and to less than 50% of baseline cortisol concentration in 10 of 14 dogs with PDH. Suppression, as identified by these 2 criteria, was not observed at 2, 4, 6, or 8 hours after administration of either dexamethasone preparation in dogs with adrenocortical tumor. For both protocols, the 8-hour plasma cortisol concentration was suppressed to less than 1.4 micrograms/dl and to less than 50% of baseline in the 5 control dogs. Both protocols were comparable for use as screening tests in establishing a diagnosis of hyperadrenocorticism. Suppression of plasma cortisol concentration to less than 50% of baseline (or less than 1.4 micrograms/dl) during the test was consistent with diagnosis of PDH. Failure to have such suppression, however, was observed in dogs with PDH as well as in those with adrenocortical tumor.  相似文献   

15.
Objective To investigate the effect of 0.02% tacrolimus in aqueous suspension on tear production in dogs with keratoconjunctivitis sicca (KCS). Animals studied One hundred five dogs diagnosed with KCS [Schirmer tear test (STT) ≤ 10 mm/min and clinical signs of dry eye]. Eyes with marginally decreased STT (11 ≤ 15 mm/min) and clinical signs of dry eye were also evaluated. Procedure The investigation was conducted in two parts: an initial efficacy study and a subsequent double blinded controlled study. In the efficacy study, the effect of topical tacrolimus (formerly FK‐506) on tear production in dogs with primary KCS was evaluated. Dogs were divided into four categories: 1) 59 eyes (38 dogs) naïve to tear stimulation therapy with initial STT ≤ 10 mm/min; 2) 28 eyes (21 dogs) naïve to tear stimulation therapy with initial STT 11 ≤ 15 mm/min; 3) 30 eyes (15 dogs) maintained successfully on CsA therapy; 4) 47 eyes (24 dogs) unresponsive to CsA therapy. STT and clinical signs were evaluated prior to and after 6 to 8 weeks of twice daily tacrolimus administration. Tacrolimus was substituted for CsA therapy in categories 3 and 4. The controlled study compared the effect of topical tacrolimus in aqueous suspension to administration of the aqueous carrier alone on tear production in 20 dogs with primary KCS. Results In the efficacy study, STT increased by 5 mm/min in 84.7%, 25.0%, 26.7% and 51.1% of eyes in categories 1, 2, 3 and 4 respectively after tacrolimus administration. Eighty‐three percent of eyes with extremely low initial STT (≤ 2 mm/min), increased 5 mm/min after tacrolimus. In the controlled study, STT increased by 5 mm/min in 7/10 dogs (14/20 eyes) that received tacrolimus and in none of the 10 dogs that received aqueous carrier alone. Dogs receiving just the aqueous carrier were subsequently treated with tacrolimus, and STT increased 5 mm/min in 9 dogs (18/20 eyes) after administration. Conclusions Twice daily administration of 0.02% tacrolimus in aqueous suspension effectively increased tear production in dogs with KCS. Topical tacrolimus is a promising alternative to topical CsA for treatment of KCS and may be beneficial in patients with less than optimal response to topical CsA.  相似文献   

16.
OBJECTIVE: To evaluate effects of trimethoprim-sulfamethoxazole (T/SMX) on thyroid function in dogs. ANIMALS: 6 healthy euthyroid dogs. PROCEDURE: Dogs were administered T/SMX (14.1 to 16 mg/kg, PO, q 12 h) for 3 weeks. Blood was collected weekly for 6 weeks for determination of total thyroxine (TT4), free thyroxine (fT4), and canine thyroid-stimulating hormone (cTSH) concentrations. Schirmer tear tests were performed weekly. Blood was collected for CBC prior to antimicrobial treatment and at 3 and 6 weeks. RESULTS: 5 dogs had serum TT4 concentrations equal to or less than the lower reference limit, and 4 dogs had serum fT4 less than the lower reference limit after 3 weeks of T/SMX administration; cTSH concentrations were greater than the upper reference limit in 4 dogs. All dogs had TT4 and fT4 concentrations greater than the lower reference limit after T/SMX administration was discontinued for 1 week, and cTSH concentrations were less than reference range after T/SMX administration was discontinued for 2 weeks. Two dogs developed decreased tear production, which returned to normal after discontinuing administration. CONCLUSIONS AND CLINICAL RELEVANCE: Results suggest that administration of T/SMX at a dosage of 14.1 to 16 mg/kg, PO, every 12 hours for 3 weeks caused decreased TT4 and fT4 concentrations and increased cTSH concentration, conditions that would be compatible with a diagnosis of hypothyroidism. Therefore, dogs should not have thyroid function evaluated while receiving this dosage of T/SMX for >2 weeks. These results are in contrast to those of a previous study of trimethoprim-sulfadiazine.  相似文献   

17.
OBJECTIVE: To evaluate effects of anesthesia, surgery, and intravenous administration of fluids on plasma concentrations of antidiuretic hormone (ADH), concentration of total solids (TS), PCV, arterial blood pressure (BP), plasma osmolality, and urine output in healthy dogs. ANIMALS: 22 healthy Beagles. PROCEDURE: 11 dogs did not receive fluids, and 11 received 20 ml of lactated Ringer's solution/kg of body weight/h. Plasma ADH adn TS concentrations, PCV, osmolality, and arterial BP were measured before anesthesia (T0) and after administration of preanesthetic agents (T1), induction of anesthesia (T2), and 1 and 2 hours of surgery (T3 and T4, respectively). Urine output was measured at T3 and T4. RESULTS: ADH concentrations increased at T1, T3, and T4, compared with concentrations at T0. Concentration of TS and PCV decreased at all times after administration of preanesthetic drugs. Plasma ADH concentration was less at T3 in dogs that received fluids, compared with those that did not. Blood pressure did not differ between groups, and osmolality did not increase > 1% from To value at any time. At T4, rate of urine production was less in dogs that did not receive fluids, compared with those that did. CONCLUSIONS AND CLINICAL RELEVANCE: Plasma ADH concentration increased and PCV and TS concentration decreased in response to anesthesia and surgery. Intravenous administration of fluids resulted in increased urine output but had no effect on ADH concentration or arterial BP. The causes and effects of increased plasma ADH concentrations may affect efficacious administration of fluids during the perioperative period in dogs.  相似文献   

18.
Retrograde flow of spermatozoa into the urinary bladder of dogs during ejaculation or after administration of xylazine was examined. In experiment 1, the mean (+/- SD) spermatozoal concentration in urine collected by cystocentesis before ejaculation was 0.322 +/- 0.645 X 10(6)/ml. After ejaculation, motile spermatozoa were present in the urine collected by cystocentesis from 12 of 15 dogs, and the concentration of spermatozoa in the urine (5.139 +/- 7.014 X 10(6)/ml) was higher (P less than 0.025) than the concentration in the urine collected before ejaculation. The percentage of the total number of spermatozoa that were displaced during ejaculation and flowed into the urinary bladder (retrograde flow) ranged from 0 to 99.75% (24.67 +/- 33.98%). In experiments 2 and 3, administration of xylazine to sexually rested dogs induced retrograde flow of spermatozoa into the urinary bladder. In experiment 2, all dogs had spermatozoa in urine collected after xylazine administration, with motile spermatozoa present in the urine from 9 of 10 dogs. In experiment 3, urine collected from dogs before administration of xylazine was azoospermic or contained few, nonmotile spermatozoa (0.063 +/- 0.135 X 10(6)/ml), whereas urine collected after administration of xylazine had more (P less than 0.025) and motile spermatozoa (3.717 +/- 4.273 X 10(6)/ml). In experiment 4, administration of xylazine to dogs after ejaculation did not increase the concentration of spermatozoa in the urine. Results indicate that spermatozoa flow into the urinary bladder of dogs during ejaculation or after administration of xylazine to sexually rested dogs.  相似文献   

19.
The hemolytic effect of onion consumption in dogs with hereditary high erythrocyte reduced glutathione and potassium concentrations (designated HK dogs) was compared with that in clinically normal dogs. Twelve hours after oral administration of boiled onions (200 g/dog), hemoglobin concentration decreased to 84.4% of the initial value in HK dogs; it decreased only to 90.5% in clinically normal dogs. At 24 hours, methemoglobin concentration was significantly (P less than 0.05) higher in HK dogs than in clinically normal dogs. The concentration of erythrocyte oxidized glutathione increased about fivefold at 10 hours in HK dogs, whereas it did not change during the experimental period in clinically normal dogs. In addition, at 12 hours, the proportion of erythrocytes containing Heinz bodies increased to 24.4% in HK dogs, but increased only to 1.2% in clinically normal dogs. Thus, results indicated that HK dogs were more susceptible to the oxidant action of onions than were clinically normal dogs.  相似文献   

20.
Pituitary-adrenal function was assessed by a combined dexamethasone suppression-ACTH stimulation test in 15 diabetic and 9 healthy dogs. In both groups, plasma cortisol concentrations decreased (P less than 0.001) after dexamethasone administration and increased (P less than 0.001) after ACTH administration. Differences between groups (P greater than 0.05) and group-by-time interactions were not significant (P greater than 0.05). Seemingly, adrenal function was not altered in well-regulated diabetic dogs.  相似文献   

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