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首页> 外文期刊>Indian Journal of Animal Health >PROTECTIVE EFFECT OF A POTENTIAL POLYHERBAL DRUG ON MAMMARY TISSUE DAMAGE CAUSED BY INTRAMAMMARY ADMINISTRATION OF ANTIBIOTIC BY PRODUCING ANTIOXIDANT ACTION
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PROTECTIVE EFFECT OF A POTENTIAL POLYHERBAL DRUG ON MAMMARY TISSUE DAMAGE CAUSED BY INTRAMAMMARY ADMINISTRATION OF ANTIBIOTIC BY PRODUCING ANTIOXIDANT ACTION

机译:潜在的抗药性药物对哺乳动物组织产生抗氧化剂作用引起的乳腺组织损伤的保护作用

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摘要

The study was aimed to evaluate the effect of intramammary administration of ceftriaxone (antibiotic) on milk enzyme activites to assess mammary gland tissue damage and oxidative stress and to observe the effect of a poly herbal drug (Fibrosin~R) on milk enzyme activites by one hour prior oral dosing to single intramammary administration of ceftriaxone. A total of twelve healthy lactating goats were divided into two groups (Gr-I and Gr-II) each containing six goats. A single dose of ceftriaxone dissolving in 5 ml of distilled water was divided into 2 equal portions and administered to each quarter of goats of Gr-I intracisternally at 50 mg/kg body weight A half bolus of Fibrosin8 was orally administered one hour prior to intramammary administrationof ceftriaxone at 50 mg/kg body weight to goats of Gr-II. Milk alkaline phospatase activity was increased gradually until 96 hour for the antibiotic treated group indicating mammary gland tissue damage. However, the enzyme activity returned to its normallevel in Fibrosin~R treated Gr-II goats at 96 hour postdosing of Fibrosin~R. Only intramammary antibiotic administration lowered milk GSH level at 6 hour, but thereafter steadily increased reduced glutathione (GSH) level until 96 hour. But the polyherbal treatment maintained a normal range of milk reduced glutathione. Milk Catalase activity gradually increased until 48 hour and decreased afterward until 96 hour postdosing for group L Whereas the enzyme activity increased until 24 hour, afterward decreased at 48 hour and again increased from 72 hour to 96 hour with the polyherbal treatment signifying antioxidant activity of Fibrosin~R.
机译:该研究旨在评估头孢曲松(抗生素)在乳房内的给药对乳酶活性的影响,以评估乳腺组织损伤和氧化应激,并观察一种多草药(Fibrosin〜R)对乳酶活性的影响。口服给药前1小时至头孢曲松单次乳房内给药。将总共​​十二只健康的哺乳山羊分成两组(Gr-I和Gr-II),每组包含六只山羊。将溶解在5 ml蒸馏水中的单剂头孢曲松分成两等份,以每头体重50 mg / kg的体重将其每四分之一的Gr-1山羊腹腔内给药。在乳房内给药前一小时口服一次半剂量的Fibrosin8。以50 mg / kg体重的头孢曲松钠对Gr-II山羊的给药。抗生素处理组的牛奶碱性磷酸酶活性逐渐增加,直至96小时,表明乳腺组织受损。然而,在Fibrosin〜R给药96小时后,在Fibrosin〜R处理的Gr-II山羊中,酶活性恢复到正常水平。仅乳房内施用抗生素可在6小时内降低牛奶的GSH水平,但此后一直稳定地增加降低的谷胱甘肽(GSH)水平,直到96小时。但是,多草药治疗可以使牛奶中的谷胱甘肽减少保持正常范围。对于L组,牛奶过氧化氢酶活性逐渐增加直至48小时,之后降低至96小时,而酶活性增加直至24小时,此后在48小时降低,然后再从72小时增加至96小时,其中多草药处理表明纤维蛋白的抗氧化活性〜R。

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