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[The effect of dopaminergic pharmacological agents on the pancreatic islet apparatus in rats]. [多巴胺能药物对大鼠胰岛器官的影响]。
N Boiadzhieva

Experimental studies were carried out on white male sexual mature healthy rats with induced alloxan diabetes, to clarify the role of dopaminergic system in the regulation of functions of the insular apparatus of the pancreas. The experiments were performed by the following drugs: bromrcripine, levodopa, a combination of revodopa plus carbidopa and haloperidol. Parameters of carbohydrate metabolism were determined in the course of acute and chronic experiments. The results sustained the hypothesis for participation of dopaminergic system in the regulation of production and secretion of insulin and respectively in the control of carbohydrate metabolism. Independent studies were carried out on white rats with alloxan diabetes after combined administration of dopaminergic pharmacological drugs and sulphanylureic preparation (SUP)-glybenclimide. The mechanisms of interaction after the combined administration of the investigated drugs under the conditions of experimental diabetes mellitus were clarified. The obtained results supplement data, in support of the hypothesis for the role of dopamine as a neuromediator in the regulation of the insular apparatus of the pancreas.

以四氧嘧啶型糖尿病诱导的雄性白种性成熟健康大鼠为实验对象,探讨多巴胺能系统在胰岛器功能调节中的作用。实验采用溴克里平、左旋多巴、revodopa + carbidopa、haloperidol联合用药。在急性和慢性实验过程中测定碳水化合物代谢参数。这些结果支持了多巴胺能系统参与胰岛素产生和分泌的调节以及碳水化合物代谢的控制的假设。对四氧嘧啶型糖尿病大鼠联合给予多巴胺能药物和磺胺脲制剂(SUP)-格列苄胺后进行了独立研究。阐明了实验糖尿病患者联合用药后相互作用的机制。所获得的结果补充了数据,支持多巴胺作为神经介质在胰腺岛体调节中的作用的假设。
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引用次数: 0
[Liposomal systems--prospective drug forms. II. The creation and characterization of liposomal systems for the oral use of narcotic analgesics]. 脂质体系统——未来的药物形式。2用于口服麻醉镇痛药的脂质体系统的创建和表征。
S Mikhaĭlova, K Iakimova

Liposomal systems were prepared for oral usage of narcotic analgesics morphine and phentanyl. The systems were examined for homogeneity in respect to seize size and form of liposomal structures by a diffraction-laser method and electron microscopy. The liposomal drug forms were studied on biological experiment as the change in the body temperature of rats was described. It was established that in rats oral usage of liposomal systems with morphine respectively with phentanyl caused significantly better effect in comparison with active substances, not taken in liposomes.

制备了用于麻醉镇痛药吗啡和芬太尼口服的脂质体系统。通过衍射激光方法和电子显微镜检查了该系统在脂质体结构的大小和形式方面的均匀性。通过生物实验研究了脂质体药物形态,描述了大鼠体温的变化。结果表明,大鼠分别口服含吗啡和芬太尼的脂质体系统,其效果明显优于未在脂质体中服用的活性物质。
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引用次数: 0
[Acute-phase changes in ceruloplasmin after gamma-ray irradiation]. [γ射线照射后铜蓝蛋白急性期变化]。
E Aladzhov, A Logofetov

The change of ceruloplasmin level of blood serum of guinea-pigs was studied on the 12th h after irradiation with gamma-rays from 60Co, using doses of 1-10 Gy, power of the dose of 0.68 Gy/min. The enzyme level was raised by the increase of the irradiation dose as it was reduced by the dose of 10 Gy in comparison with the control animals. This was probably due to inactivation of the molecules of ceruloplasmin by radicals and peroxides, obtained by this hyperlethal dose. Sera proteins showed a change in the increase of the dose: a reduction of albumins and an increase in beta- and gamma-globulins. Alpha-2-globulins, with which ceruloplasmin moved electrophoretically at low doses, showed slowly a slow increase in comparison with the control value, but at high doses-phase globulins. Oxidase activity of ceruloplasmin was determined by 01 todianisidine, but sera proteins-by agarose electrophoresis. The level of s ceruloplasmin in animals, irradiated by LD50 = 4.1 Gy, showed chronological change-an increase at early periods, maximum on the 12th h and a reduction at late periods close to the normal range. The level of serum copper followed the change in the enzyme level by analogy.

用60Co γ射线辐照豚鼠,剂量为1 ~ 10 Gy,辐照功率为0.68 Gy/min,观察辐照12 h后豚鼠血清铜蓝蛋白水平的变化。与对照动物相比,辐照剂量增加使酶水平升高,而10 Gy剂量则使酶水平降低。这可能是由于这种高致死剂量获得的自由基和过氧化物使铜蓝蛋白分子失活。血清蛋白在剂量增加时表现出变化:白蛋白减少,β -和γ -球蛋白增加。α -2-球蛋白,在低剂量时铜蓝蛋白在电泳上移动,与对照值相比,显示出缓慢的缓慢增加,但在高剂量期球蛋白。铜蓝蛋白氧化酶活性测定用01 -二苯胺法,血清蛋白测定用琼脂糖电泳法。LD50 = 4.1 Gy辐照动物体内s -铜蓝蛋白水平呈时间变化,早期升高,12 h达到最高值,后期下降,接近正常范围。血清铜水平随酶水平的变化而变化。
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引用次数: 0
[Experimental research on the toxicity of pharmapentoxifylline (II)]. [药芪酮茶碱毒性的实验研究(二)]。
M Koleva, N Donchev, B Borov, V Dzharova

The results from morphological studies on liver, lung, heart, spleen, intestine, brain, skin, testes (ovaries), obtained in the end of the first and third month of animals, treated with pharmapentoxiphyline (PP), are described. The experiments were carried out on 312 white rats (male and female), divided into 2 series: I series--oral usage of the preparation in doses of 100, 300 and 6 mg/kg, II series--intraperitoneal administration in doses of 30, 75 and 150 mg/kg. It was established that PP, administered for a period of 3 months orally in a dose of 100 mg/kg and intraperitoneally in a dose of 30 mg/kg did not induced changes in the structure of all examined organs. Slight dystrophic changes in liver, lung and spleen occurred in the end of the third month under the influence of an oral dose of 300 mg/kg and an intraperitoneal dose of 75 mg/kg. The obtained results are discussed in connection with the pharmacological action of drug-peripheral vasodilatator.

本文描述了在给药后第一个月和第三个月末对动物的肝、肺、心、脾、肠、脑、皮肤、睾丸(卵巢)进行形态学研究的结果。实验以雄性和雌性大鼠312只为实验对象,分为2个系列:I系列-口服剂量为100、300和6 mg/kg, II系列-腹腔剂量为30、75和150 mg/kg。经证实,PP以100mg /kg的口服剂量和30mg /kg的腹腔剂量给药3个月,不会引起所有被检查器官的结构变化。在口服剂量为300 mg/kg和腹腔剂量为75 mg/kg的影响下,在第三个月末出现肝、肺和脾的轻微营养不良变化。并结合药物外周血管扩张剂的药理作用对所得结果进行了讨论。
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引用次数: 0
[Anti-islet antibodies: methods for their determination and etiopathogenetic importance]. [抗胰岛抗体:测定方法及其发病意义]。
M Velinov
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引用次数: 0
[Experimental research on the toxicity of pharmapentoxifylline (I)]. [药芪酮茶碱毒性的实验研究(一)]。
M Koleva, N Donchev, N Udvareva, V Dzharova

Results from the study on acute, subacute and chronic toxicity of the therapeutic preparation pharmapentoxiphyline (PP), produced by Pharmachem, are described. The experiments were carried out on 312 male and female white rats. According to the limiting index of LD50 with, Oral dose of (1220 mg/kg of body mass for male rats and 1050 mg/kg for female rats) and intraperitoneal PP dose of PP (230 mg/kg for female rats and 235 mg/kg for female rats) it was included into IV class of slightly toxic compounds. Doses of 100, 300 and 600 mg/kg/oral administration) and 30, 75 and 150 mg/kg (intraperitoneal administration) were used in subacute and chronic experiments. Integral, hematological and biochemical methods and parameters were applied for evaluation of the toxic effect. There was no hemato-, hepato- and nephrotoxicity after oral and intraperitoneal administration of PP in doses of 10 and 30 mg/kg for a period of 3 months. Some recommendations, which should be taken into consideration during continuous treatment with PP, are given on the basis of a complex evaluation of the results from the hematological parameters.

本文介绍了Pharmachem公司生产的治疗制剂pharmapentoxiphyline (PP)的急性、亚急性和慢性毒性的研究结果。实验以雌雄大鼠312只为实验对象。根据LD50极限指数,口服剂量为(雄性大鼠体重1220 mg/kg,雌性大鼠体重1050 mg/kg),腹腔PP剂量为PP(雌性大鼠230 mg/kg,雌性大鼠235 mg/kg),归为IV类微毒化合物。亚急性和慢性实验分别采用100、300和600 mg/kg(口服)和30、75和150 mg/kg(腹腔)给药。采用积分、血液学、生化等方法及参数评价毒副作用。口服和腹腔注射剂量分别为10和30 mg/kg的PP 3个月后,没有出现血液、肝脏和肾毒性。在对血液学参数结果进行复杂评估的基础上,提出了一些建议,这些建议应在PP持续治疗期间予以考虑。
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引用次数: 0
[The pathomorphological changes in the pleura of rabbits with artificial pneumothorax and uropolin pleurography]. [人工气胸兔胸膜病理形态学变化及尿蛋白胸膜造影]。
I Dakov, V Vlasov, V Marinov

The results from artificial pneumothorax in 25 rabbits with intrapleural administration of Uropolin (10 rabbits) as well as of 10% solution of NACl (7 rabbits) were described. Thoracotomy was made on 7th, 14th and 12 21st day and the parietal, diaphragmatic and visceral pleura with underlaying tissues were examined. Proliferation of the mesothelium [correction of mesother] and growth of the connective tissue, which were more manifested in rabbits treated with Uropolin, were established histologically. The authors think that pathohistological examinations confirm the clinical observed favourable effect of intrapleural administration of Uropolin for obliteration of the pleural cavity.

本文报道25只家兔胸膜内注射尿孢素(10只)和10% NACl溶液(7只)人工气胸的结果。于第7天、第14天、第12天、第21天开胸,检查胸膜壁层、膈层、内脏层及下层组织。组织学观察发现,间皮的增殖和结缔组织的生长在经尿孢素处理的家兔中更为明显。作者认为,病理组织学检查证实了临床观察到的胸腔内给药乌polin对胸膜腔闭塞的有利效果。
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引用次数: 0
[The cytofluorimetric characteristics of monoclonal antibodies for use in humans in respect of their activity and cross reactivity]. [用于人的单克隆抗体在活性和交叉反应性方面的细胞荧光特性]。
G Davidkova, Kh Taskov, E Dimitrova, G Gencheva

A cytofluorimetric method for determination of the reactivity of antimyeloma MkAt 225,28S with myeloma cells and blood elements is described in the present article. The obtained results show that the antibody possesses high specific activity and does not bind with normal human lymphocytes, monocytes, granulocytes, thrombocytes and erythrocytes in the examined dilutions. The method is suitable for control of cross reactivity with blood cells of MkAt preparations for usage in subjects.

本文描述了一种测定抗骨髓瘤MkAt 225、28S与骨髓瘤细胞和血液元素反应性的细胞荧光法。结果表明,该抗体具有很高的特异性活性,在检测的稀释度中不与正常人淋巴细胞、单核细胞、粒细胞、血小板和红细胞结合。本方法适用于受试者使用的MkAt制剂与血细胞交叉反应性的控制。
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引用次数: 0
[Morphometric research on the germ and Sertoli cells in prespermatogenesis]. [精子前发育过程中胚芽和支持细胞形态计量学研究]。
P Tsvetkova

The author investigated the changes in the morphology of germinative and Sertoli's cells during prespermatogenesis of the rat. This problems were studied by morphometric investigations in 20 rats of Wistar strain, divided into age groups: newborns, 5, 10 and 15 postnatal days. The morphofunctional characteristic of these two types of cellular populations in immature rats showed existence of parallelism in the proliferation of these cells, the level of organization and interrelationships between them, which was of substantial significance for creation and further maintenance of an optimal microenvironment, needed for differentiation of sex cells.

作者研究了大鼠精子前发生过程中萌发细胞和支持细胞形态的变化。以Wistar品系20只大鼠为研究对象,分为新生儿、出生后5天、10天和15天。这两种细胞群在未成熟大鼠体内的形态功能特征表明,这两种细胞在增殖、组织水平和相互关系上存在相似性,这对性细胞分化所需的最佳微环境的创造和进一步维持具有重要意义。
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引用次数: 0
[Insulin-like growth factors]. 胰岛素样生长因子。
V Mitev, L Sirakov
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引用次数: 0
期刊
Eksperimentalna meditsina i morfologiia
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