吳 彤,張道康,劉茂林,黃慧麗,張 寧,徐 飛,劉義明
(1南京農(nóng)業(yè)大學(xué)生命科學(xué)院,南京 210095;2中國(guó)農(nóng)業(yè)科學(xué)院飼料研究所,北京 100081;3中國(guó)農(nóng)業(yè)大學(xué)動(dòng)物醫(yī)學(xué)院,北京 100094)
硫酸頭孢喹肟乳房注入劑(干乳期)對(duì)奶牛安全性的研究
吳 彤1,張道康2,劉茂林2,黃慧麗2,張 寧3,徐 飛2,劉義明2
(1南京農(nóng)業(yè)大學(xué)生命科學(xué)院,南京 210095;2中國(guó)農(nóng)業(yè)科學(xué)院飼料研究所,北京 100081;3中國(guó)農(nóng)業(yè)大學(xué)動(dòng)物醫(yī)學(xué)院,北京 100094)
【目的】了解硫酸頭孢喹肟乳房注入劑(干乳期)對(duì)健康奶牛的正常體溫、日產(chǎn)奶量、奶中體細(xì)胞數(shù)和乳房?jī)?nèi)菌群的影響?!痉椒ā窟x用初產(chǎn)和經(jīng)產(chǎn)健康泌乳期奶牛各6頭,所選奶牛在試驗(yàn)前30 日內(nèi)未全身性或乳房?jī)?nèi)給予任何抗生素,奶牛正常飼養(yǎng)管理,日糧和飲水中不含有任何抗菌藥物。給藥前1 和0日統(tǒng)計(jì)記錄各試驗(yàn)?zāi)膛5闹蹦c溫度、日產(chǎn)奶量(早、中、晚3 次產(chǎn)奶量的加和)、檢測(cè)每個(gè)乳區(qū)采集奶樣的體細(xì)胞數(shù),并對(duì)給藥前0日的奶樣進(jìn)行病原菌分離鑒定。4個(gè)乳區(qū)分別單次給予硫酸頭孢喹肟乳房注入劑(干乳期)。給藥后的第1、3、5、7、10天分別統(tǒng)計(jì)記錄每頭奶牛的日產(chǎn)奶量,給藥后的第12 h、3、5、7、10天分別采集奶樣進(jìn)行體細(xì)胞檢測(cè),同時(shí)檢查直腸溫度;給藥后的第10天,采集奶樣進(jìn)行病原菌分離鑒定。比較奶牛用藥前后直腸溫度、日產(chǎn)奶量、牛奶體細(xì)胞數(shù)和奶中病原菌的變化。整個(gè)試驗(yàn)期間連續(xù)觀察給藥奶牛是否出現(xiàn)紅、腫、熱、痛等臨床癥狀。【結(jié)果】給藥前1天、0天和最后一次給藥后的第1、3、5、7、10天,試驗(yàn)?zāi)膛5娜债a(chǎn)奶量平均值分別為28.8、27.7、28.1、28.7、28.8、29.2和29.6 kg,卡方檢驗(yàn)顯示無顯著性差異(P>0.05);各時(shí)間點(diǎn)采集的奶中體細(xì)胞數(shù)大都維持在30—50萬個(gè)/mL之間;各時(shí)間點(diǎn)測(cè)得的奶牛直腸溫度平均值分別為38.3、38.4、38.3、38.3、38.3、38.2和38.3℃,無顯著性差異(P>0.05);病原菌檢測(cè)結(jié)果顯示,在給藥前0 日采集的奶樣中,分離到大腸桿菌8株、鏈球菌5株和葡萄球菌7株,給藥后第10天采集的奶樣中大腸桿菌、鏈球菌和葡萄球菌各分離到1株,明顯減少,且沒有增加新的病原菌?!窘Y(jié)論】硫酸頭孢喹肟乳房注入劑(干乳期)對(duì)奶牛正常體溫、產(chǎn)奶量和奶中體細(xì)胞數(shù)等沒有不良影響,該制劑用于奶牛是安全的。
硫酸頭孢喹肟乳房注入劑;干乳期;安全性;體細(xì)胞數(shù)
【研究意義】乳房炎又稱乳腺炎,是由各種原因引起的乳房炎癥,其主要特點(diǎn)是乳汁發(fā)生理化性質(zhì)及細(xì)菌學(xué)變化,乳腺組織發(fā)生病理學(xué)變化[1-2]。乳房炎是奶牛最常見的疾病之一,由于乳房炎造成奶牛產(chǎn)奶量下降、治療費(fèi)用增加、治療期間牛奶廢棄以及奶牛過早淘汰等問題給奶牛養(yǎng)殖業(yè)帶來巨大經(jīng)濟(jì)損失[3-4],嚴(yán)重困擾著奶牛養(yǎng)殖業(yè)的健康發(fā)展,同時(shí)也給乳制品的質(zhì)量造成一定影響。盡管各國(guó)學(xué)者專家從未停止過對(duì)奶牛乳房炎的研究,但是目前該病還無法根治。據(jù)報(bào)道,全球奶牛30%患有乳房炎,隱性乳房炎的患病率達(dá)50%以上[5]。引起奶牛乳房炎的原因多種多樣,其中,病原菌感染是一個(gè)非常重要的因素,常見病原菌有大腸桿菌、金黃色葡萄球菌和鏈球菌等[6-7]。奶牛干乳期由于乳腺生理機(jī)能的調(diào)整和變化,干乳初期和干乳后期乳管開放,乳腺的抵抗力明顯下降,病原菌容易乘虛而入。因此干乳期是奶牛乳房炎新增感染的高發(fā)期[8],尤其是隱性乳房炎,通常難以發(fā)現(xiàn),等到泌乳開始后才表現(xiàn)出臨床癥狀,此時(shí)發(fā)現(xiàn)為時(shí)已晚。因此在泌乳結(jié)束即將進(jìn)入干乳期時(shí)給奶牛用藥能有效的預(yù)防和治療干乳期乳房炎[9-10]。目前國(guó)內(nèi)用于干乳期治療乳房炎的藥物相對(duì)較少,為提高干乳期奶牛乳房炎的防治效果,降低養(yǎng)殖成本,提高養(yǎng)殖效益,國(guó)家飼料藥物基準(zhǔn)實(shí)驗(yàn)室成功研制了硫酸頭孢喹肟乳房注入劑(干乳期),為將該制劑應(yīng)用于奶牛乳房炎的臨床治療,本文對(duì)硫酸頭孢喹肟乳房注入劑(干乳期)用于奶牛的安全性進(jìn)行了試驗(yàn)研究?!厩叭搜芯窟M(jìn)展】頭孢喹肟由德國(guó)赫斯特公司于20世紀(jì)80年代開發(fā),1993年首次批準(zhǔn)上市,英國(guó)英特威公司于1994年研制成功頭孢喹肟混懸劑和軟膏[11-12]。頭孢喹肟是第一個(gè)也是目前唯一一個(gè)動(dòng)物專用的第四代頭孢類抗生素[13]。頭孢喹肟抗菌譜廣,抗菌活性強(qiáng),對(duì)β內(nèi)酰胺酶穩(wěn)定[14-15],藥代動(dòng)力學(xué)特性優(yōu)良[16-17],毒副作用小[18-19],在國(guó)內(nèi)外已廣泛用于奶牛乳腺炎、子宮內(nèi)膜炎和豬、牛、馬呼吸道感染等疾病的臨床治療[20-23]。GUERIN-FAUDEE等[24]研究了頭孢喹肟對(duì)引起奶牛乳房炎的495株G+菌、G-菌的抗菌活性,發(fā)現(xiàn)頭孢喹肟不僅對(duì)臨床分離的各種G+菌、G-菌有較強(qiáng)的抗菌活性,而且對(duì)綠膿桿菌有強(qiáng)大的抗菌活性。PENGOV等[25]等發(fā)現(xiàn),頭孢喹肟按75 mg/次劑量連續(xù)灌注3次(間隔12 h),對(duì)金黃色葡萄球菌單獨(dú)感染、金黃色葡萄球菌和鏈球菌混合感染引起的奶牛乳房炎都有很好的療效。國(guó)外關(guān)于頭孢喹肟用于泌乳期奶牛乳房炎治療的注入劑已取得了良好的臨床效果?!颈狙芯壳腥朦c(diǎn)】奶牛即將進(jìn)入干乳期時(shí),乳房?jī)?nèi)用藥能有效預(yù)防和治療干乳期乳房炎,為下一個(gè)泌乳期提供保障。目前國(guó)內(nèi)市場(chǎng)上還沒有專門用來預(yù)防和治療奶牛乳房炎的干乳期用硫酸頭孢喹肟乳房注入劑?!緮M解決的關(guān)鍵問題】按推薦劑量給健康奶牛注入硫酸頭孢喹肟乳房注入劑(干乳期),通過對(duì)比用藥前后奶牛的直腸溫度、產(chǎn)奶量、奶中體細(xì)胞數(shù)及奶中病原菌數(shù)量來驗(yàn)證該制劑對(duì)奶牛的安全性。
1.1 受試藥物
硫酸頭孢喹肟乳房(干乳期)注入劑,規(guī)格:150 mg:3 g/支;批號(hào)20120601;有效期:2年;由中國(guó)農(nóng)業(yè)科學(xué)院飼料研究所提供,推薦干乳期奶牛每頭每個(gè)乳區(qū)給藥1支。
1.2 試驗(yàn)動(dòng)物
經(jīng)產(chǎn)和初產(chǎn)健康泌乳期奶牛各6 頭,產(chǎn)奶量在20—35 kg·d-1之間,在試驗(yàn)前30 日內(nèi)未全身性或乳房?jī)?nèi)給予抗生素。
1.3 給藥
奶牛擠奶后,先用消毒毛巾清潔各乳區(qū),再用消毒藥液浸泡乳頭約30 s,然后乳頭內(nèi)給藥,每個(gè)乳區(qū)各注入硫酸頭孢喹肟乳房注入劑(干乳期)一支,給藥1 次。灌注時(shí)將含藥推注管頭插入乳頭,輕輕推壓活塞,將藥物緩緩注入乳池內(nèi),隨后輕輕按摩相應(yīng)乳區(qū),使藥物均勻分布。
1.4 直腸溫度檢查
給藥前1 日、給藥當(dāng)日和給藥后第12 h,3、5、7、10天,測(cè)量并記錄試驗(yàn)?zāi)膛5闹蹦c溫度。
1.5 日產(chǎn)奶量測(cè)量
給藥前1 日、給藥當(dāng)日和給藥后第1、3、5、7、10天記錄奶牛的日產(chǎn)奶量。每頭奶牛每日早、中、晚各擠奶1次,每頭奶牛每次擠奶匯入專用收集桶中,稱重并記錄。根據(jù)每頭奶牛每日3 次總產(chǎn)奶量(即日產(chǎn)奶量),計(jì)算12 頭奶牛的平均日產(chǎn)奶量。
1.6 乳中體細(xì)胞數(shù)檢測(cè)
給藥前1天、給藥當(dāng)天和給藥后第12 h,3、5、7、10天,4個(gè)乳區(qū)分別采集奶樣,每次擠奶前棄掉前3把奶,將奶樣采集至50 mL滅菌離心管中,進(jìn)行體細(xì)胞計(jì)數(shù)。
1.7 病原菌分離和鑒定
分別在給藥前0天和給藥后第10天各采集奶樣1次(20 mL)進(jìn)行細(xì)菌學(xué)檢查。采樣時(shí)先用清水沖洗乳房,用0.1%新潔爾滅或者75%乙醇對(duì)乳頭及周圍進(jìn)行消毒,待酒精揮發(fā)后,手工擠奶,棄去前3把奶后,采集奶樣于滅菌試管中,4 ℃保存并于6 h內(nèi)送實(shí)驗(yàn)室進(jìn)行細(xì)菌分離、鑒定。
將各奶樣接種至選擇性培養(yǎng)基分離各種病原菌。分離菌株經(jīng)純化培養(yǎng)后,依據(jù)菌落形態(tài)、染色特征、生化特點(diǎn)鑒定其種類。
1.8 臨床癥狀觀察
整個(gè)試驗(yàn)過程中,每日觀察、記錄各試驗(yàn)?zāi)膛5呐R床癥狀。一旦出現(xiàn)臨床癥狀立即采取相應(yīng)措施。
1.9 統(tǒng)計(jì)分析
利用SPSS統(tǒng)計(jì)學(xué)軟件對(duì)給藥前后直腸溫度、平均日產(chǎn)奶量、乳中體細(xì)胞數(shù)進(jìn)行卡方檢驗(yàn)。
2.1 直腸溫度
奶牛的直腸溫度見表1。所有奶牛在給藥前和給藥后不同時(shí)間點(diǎn)的直腸溫度均在正常范圍內(nèi),卡方檢驗(yàn)P>0.05,說明按推薦劑量單次給藥對(duì)奶牛的體溫?zé)o顯著影響。
2.2 日產(chǎn)奶量
12頭奶牛各時(shí)間點(diǎn)的產(chǎn)奶量見表2。硫酸頭孢喹肟乳房注入劑(干乳期)給藥后和給藥前相比,各時(shí)間點(diǎn)產(chǎn)奶量無顯著差異(卡方檢驗(yàn)P>0.05)。
表1 奶牛用藥前后直腸溫度Table1 Rectal temperature before and after treatment (℃)
表2 奶牛用藥前后的平均日產(chǎn)奶量Table2 Daily milk production before and after treatment(kg·d-1)
表3 12 頭奶牛不同乳區(qū)給藥前后奶樣中的體細(xì)胞數(shù)(萬個(gè)/mL)Table3 SCC of different udder region of 12 cows before and after treatment(10thousand/mL)
2.3 體細(xì)胞計(jì)數(shù)
體細(xì)胞計(jì)數(shù)結(jié)果見表3。12頭奶牛給藥前不同乳區(qū)體細(xì)胞檢測(cè)結(jié)果與給藥后各時(shí)間點(diǎn)奶樣中體細(xì)胞數(shù)未見明顯變化(卡方檢驗(yàn)P>0.05)。
2.4 細(xì)菌分離鑒定
在給藥前0天采集的奶樣中,分離到鏈球菌5株、葡萄球菌8 株和大腸桿菌9 株,給藥后第10日,檢測(cè)到大腸桿菌、葡萄球菌和鏈球菌各1 株(表4)。硫酸頭孢喹肟乳房注入劑(干乳期)對(duì)健康奶牛的乳房不會(huì)造成病原菌感染,而且對(duì)原有的病原菌有一定的清除能力,起到防治乳房炎的作用。
表4 用藥前后不同乳區(qū)所采奶樣細(xì)菌分離情況Table4 Pathogens of milk in different udder region before and after treatment
2.5 臨床癥狀觀察
12頭奶牛4個(gè)乳區(qū)分別單劑量乳房注入硫酸頭孢喹肟乳房注入劑(干乳期)后,在整個(gè)試驗(yàn)期間給藥乳區(qū)未出現(xiàn)乳房紅、腫、熱、痛等臨床癥狀。
續(xù)表4 Continued table4
新獸藥上市之前進(jìn)行安全性評(píng)價(jià)是藥物非臨床研究的一部分,目的是保障藥物對(duì)靶動(dòng)物、環(huán)境以及獸藥生產(chǎn)者和使用者的安全性。為此,筆者參考VICH GL43《Target Animal Safety for Veterinary Pharmaceutical Products》等國(guó)外相關(guān)指導(dǎo)原則對(duì)研制的硫酸頭孢喹肟乳房注入劑(干乳期)進(jìn)行了靶動(dòng)物安全性試驗(yàn)。通過對(duì)給藥前后牛直腸溫度、產(chǎn)奶量、乳中體細(xì)胞數(shù)及乳中病原菌的檢測(cè)和奶牛臨床癥狀觀察,證明硫酸頭孢喹肟乳房注入劑對(duì)奶牛安全。
奶牛乳房炎是奶牛重要疫病之一,據(jù)不完全調(diào)查統(tǒng)計(jì),約78%的牛場(chǎng)把乳房炎列為最重要的奶牛疫病,而干乳期乳房炎治療是控制奶牛乳房炎的重要策略之一。在奶牛干乳期間用藥,藥物不會(huì)因產(chǎn)奶而減少,對(duì)慢性乳房炎的治愈率顯著高于泌乳期間的治愈率,不僅減少新的感染機(jī)會(huì),還有利于產(chǎn)奶前乳腺組織損傷的再生修復(fù),并且還不必?fù)?dān)憂牛奶殘留問題。
筆者曾對(duì)1 398 份奶樣進(jìn)行了細(xì)菌分離和鑒定,發(fā)現(xiàn)592 份奶樣中均含有大腸桿菌、526 份奶樣中含有金黃色葡萄球菌、136 份奶樣中含有鏈球菌,說明大腸桿菌、金黃色葡萄球菌和鏈球菌是奶牛乳房炎的主要致病菌,而且流行廣泛。為此,本試驗(yàn)在干乳期用藥前后還對(duì)這3種菌進(jìn)行了分離、鑒定,并發(fā)現(xiàn)硫酸頭孢喹肟乳房注入劑能夠有效清除這3種菌的感染。
頭孢喹肟是動(dòng)物專用的第四代頭孢菌素,藥物分子在C-3′位置上有一個(gè)季銨基團(tuán),從而產(chǎn)生了兩性離子化合物,與靶標(biāo)青霉素結(jié)合蛋白有高度親合力,能夠快速穿透細(xì)胞外膜(革蘭氏陰性菌),與β內(nèi)酰胺酶親合力低,減少耐藥性的產(chǎn)生,并且增加了藥物分子穿過血膜屏障的能力,使得第四代頭孢菌素的抗菌范圍比第三代頭孢菌素更廣,而且對(duì)病原菌的敏感性比第三代有所增強(qiáng),尤其是和前幾代頭孢菌素相比,它們對(duì)革蘭氏陰性菌的抗菌譜更廣。
硫酸頭孢喹肟乳房注入劑經(jīng)乳房注入后,各時(shí)間點(diǎn)奶牛的直腸溫度、日產(chǎn)奶量及奶樣中體細(xì)胞數(shù)與給藥前相比未見明顯變化。在給藥前0 日和給藥后第10日分別采集奶樣并分離細(xì)菌,結(jié)果顯示給藥后細(xì)菌檢出數(shù)與給藥前相比降低。奶牛乳區(qū)未出現(xiàn)紅、腫、熱、痛等乳房炎癥狀和明顯不良反應(yīng)。上述結(jié)果表明,按推薦劑量單次給予硫酸頭孢喹肟乳房注入劑(干乳期),對(duì)奶牛無不良反應(yīng),安全性較高,適合奶牛乳房炎干乳期防治使用。
[1] 劉裕田. 奶牛乳房炎的發(fā)病原因及防治. 當(dāng)代畜牧,2015(23): 46-48.
LIU Y T. The etiology and prevention and control of dairy cow mastitis. Contemporary Animal Husbandry, 2015(23): 46-48.(in Chinese)
[2] 鄭丹. 奶牛乳房炎的發(fā)病原因及綜合防治措施. 農(nóng)技服務(wù), 2015,32(1):137-138.
ZHENG D. The etiology of dairy cow mastitis and comprehensive prevention and control measures. Agricultural Technology Service,2015, 32(1):137-138. (in Chinese)
[3] 倪春霞, 蒲萬霞, 胡永浩, 鄧海平, 王玲, 孟小琴. 奶牛乳房炎病原菌的分離鑒定及耐藥性分析. 西北農(nóng)業(yè)學(xué)報(bào), 2010, 19(2):20-24.
NI C X, PU W X, HU Y H, DENG H P, WANG L, MENG X Q. Isolation, identification and drug sensitive test of pathogenic bactcria causing dairy cattle mastitis. Acta Agriculturae Boreali-Occidentalis Sinica, 2010, 19(2):20-24.(in Chinese)
[4] 谷春雷. 奶牛乳房炎的發(fā)病原因及防治措施. 畜牧與飼料科學(xué),2015, 36(1):102-103.
GU C L. The etiology and prevention and control of dairy cow mastitis. Animal Husbandry and Feed Science, 2015, 36(1):102-103.(in Chinese)
[5] HERINGSTAD B, KLEMETSDAL G, RUANE J. Clinical mastitis in Norwegian cattle: Frequency, variance components and genetic correlation with protein yield. Journal of Dairy Science, 1999,82(6):1325-1330.
[6] FENLON D R, LOGUE D N, GUNN J, WILSON J. A study of mastitis bacteria and herd management practices to identify their relationship to high somatic cell counts in bulk tank milk.The British Veterinary Journal, 1995,151(1):17-25.
[7] 王玲, 李宏勝, 王正兵, 嚴(yán)作庭, 苗小樓, 陳炅然, 祁光紅, 肖俊武,張繼良. 規(guī)?;膛pB(yǎng)殖區(qū)奶牛乳房炎的調(diào)查及病因分析. 中國(guó)乳業(yè), 2010(10):50-53.
WANG L, LI H S, WANG Z B, YAN Z T, MIAO X L, CHEN J R, QI G H, XIAO J W, ZHANG J L. An investigation and analysis of reason of dairy cow mastitis. China Dairy, 2010(10):50-53.(in Chinese)
[8] DINGWELL R T, LESLIE K E, SCHUKKEN Y H, SARGEANT J M,TIMMS L L, DUFFIELD T F, KEEFE G P, KELTON D F,LISSEMORE K D, CONKLIN J. Association of cow and quarter-level factors at drying-off with new intramammary infections during the dry period. Preventive Veterinary Medicine, 2004(63): 75-89.
[9] EBERHART R J. Management of dry cows to reduce mastitis. Journal of Dairy Science, 1986, 69: 1721-1732.
[10] 史同瑞, 王爽, 吳博. 干乳期奶牛乳房炎防治與保健. 中國(guó)動(dòng)物保健, 2012, 14(1):38-40.
SHI T R, WANG S, WU B. The prevention of Dry milk cow Mastitis. China Animal Health, 2012, 14(1):38-40. (in Chinese)
[11] 劉美瑞, 趙地順, 劉寶樹, 劉林英, 汪學(xué)良, 李俊盼, 葛京京. 頭孢喹肟研究進(jìn)展. 中國(guó)畜牧獸醫(yī), 2013, 40(4):216-220.
LIU M R, ZHAO D S, LIU B S, LIU L Y, WANG X L, LI J P, GE J J. Advance of study on Cefquinome. China Animal Husbandry & Veterinary Medicine, 2013, 40(4):216-220. (in Chinese)
[12] 王付民,陳杖榴. 頭孢喹諾的研究進(jìn)展. 動(dòng)物醫(yī)學(xué)進(jìn)展, 2004,25(4):50-53.
WANG F M, CHEN Z L. Advance of study on Cefquinome. Progress in Veterinary Medicine, 2004, 25(4):50-53. (in Chinese)
[13] 俞吉杰, 余祖功, 趙杰, 劉利峰, 段復(fù)康, 江善祥. HPLC法測(cè)定硫酸頭孢喹肟?jī)龈煞坩樦辛蛩犷^孢喹肟含量. 畜牧與獸醫(yī), 2008,40(9):31-34.
YU J J, YU Z G, ZHAO J, LIU L F, DUAN F K, JIANG S X. Determination of cefquinomesulphate in cefquinomesulphate lyophilized powder by HPLC. Animal Husbandry & Veterinary Medicine, 2008, 40(9): 31-34. (in Chinese)
[14] SHPIGEL N Y, LEVIN D, WINKLER M, SARAN A, ZIV G,BOTTNER A. Efficacy of cefquinome for treatment of cows with mastitis experimentally induced using Escherichia coli. Journal of Dairy Science, 1997, 80(2):318-323.
[15] MURPHY S P,ERWINM E,JONES R N. Cefquinome (HR 11lV) in vitro evaluation of a broad-spectrum cephalosporin indicated for infections in animals. Diagnostic Microbiology and Infectious Disease,1994, 20(1):49-55.
[16] 郭亞楠, 周德剛, 李建成, 江海洋. 硫酸頭孢喹肟注射液在豬體內(nèi)的藥代動(dòng)力學(xué)及生物等效性研究. 中國(guó)獸藥雜質(zhì), 2013, 47(7): 33-37.
GUO Y N, ZHOU D G, LI J C, JIANG H Y. Pharmacokinetics and bioequivalence evaluation of cefquinome sulfate injection in pigs.Chinese Journal of Veterinary Drug, 2013, 47(7):33-37. (in Chinese)
[17] AL-TAHER A Y. Pharmacokinetics of cefquinome in camels. Journal of Animal and Veterinary Advances, 2010, 9(4):848-852.
[18] 張成. 硫酸頭孢喹肟注射液肌肉刺激性試驗(yàn). 畜牧與飼料科學(xué),2011, 32(11):53-54.
ZHANG C. Cefquinome Sulfateinjection muscle stimulation experiment. Animal Husbandry and Feed Science, 2011, 32(11): 53-54. (in Chinese)
[19] 榮俊, 張軍忍, 余祖功, 江善祥. 國(guó)產(chǎn)硫酸頭孢喹肟對(duì)小鼠的急性和蓄積毒性研究. 動(dòng)物醫(yī)學(xué)進(jìn)展, 2008, 29(2):48-51.
RONG J, ZHANG J R, YU Z G, JIANG S X. Study on acute toxicity and cumulative toxicity of domestic cefquinome sulfate in mice. Progress in Veterinary Medicine, 2008, 29(2):48-51. (in Chinese)
[20] SHPIGEL N Y,LEVIN D,WINKLER M. Efficacy of cefquinome for treatment of cows with mastitis experimentally induced using Escherichia coli. Journal of Dairy Science, 1997, 80(2):318-323.
[21] EHINGER A M, SCHMIDT H, KIETZMANN M. Tissue distribution of cefquinome after intramammary and “systemic”administration in the isolated perfused bovine udder. The Veterinary Journal, 2006,172(1): 147-153.
[22] Knappstein K, Suhren G, Walte H G. Influence of milking frequency on withdrawal period after application of lactam antibiotic-based drugs. Analytica Chimica Acta, 2003, 483(1):241-249.
[23] 馮言言, 王海挺, 鄭莉, 張智德, 孔梅, 吳連勇, 李培峰. 硫酸頭孢喹肟乳房注入劑治療奶牛乳房炎的臨床療效觀察. 中國(guó)奶牛,2014(5):28-30.
FENG Y Y, WANG H T, ZHENG L, ZHANG Z D, KONG M, WU L Y, LI P F. The study of clinical curative effect on cefquinome sulfate intramammary infusion in dairy cows. China Dairy Cattle, 2014(5): 28-30. (in Chinese)
[24] GURIN-FAUBLEE V, CARRET G HOUFFSCHMIT. In vitro activity of 10 antimicrobial agents against bacteria isolated form cows with clinical mastitis. The Verterinary Record, 2003, 152:466-471.
[25] PENGOV A. The role of coagulase-negative Staphylococcus spp. and associated somatic cell counts in the ovine mammary gland. Journal of Dairy Science, 2001, 84(3):572-574.
[26] U.S. Food and Drug Administration CVM GFI #49. Target Animal Safety and Drug Effectiveness Studies for Anti-Microbial Bovine Mastitis Products (Lactating and Non-Lactating Cow Products)[S]Revised April 4, 1996 (Revises the February 1, 1993 Guideline)
(責(zé)任編輯 林鑒非)
The Safety Evaluation of Cefquinome Sulfate Intramammary Infusion (Dry Cow)
WU Tong1, ZHANG Dao-kang2, LIU Mao-lin2, HUANG Hui-li2, ZHANG Ning3, XU Fei2, LIU Yi-ming2
(1College of Life Sciences, Nanjing Agricultural University, Nanjing 210095;2Feed Research Institute, Chinese Academy of Agricultural Sciences,Beijing 100081;3College of Veterinary Medicine, China Agricultural University, Beijing 100094)
【Objective】The objective of this study is to evaluate the effect of cefquinome sulfate intramammary infusion(dry cow) on the body temperature, milk yield per day, somatic cell counts and mammary microbiota of the health dairy cows.【Method】Six primiparous and multiparous healthy dairy cow were selected, which have not been treated with any antibiotics by systemic or intramammary administration 30 days before. They were fed with food and water without any antibiotics and under normal conditions. Rectal temperature, milk yield per day and somatic cell counts per quarter were recorded on 1 and 0 day before administration, and pathogenic bacteria were isolated and identified. After a single intramammary administration of Cefquinome Sulfate Intramammary Infusion (Dry Cow) to each quarter, milk yield was recorded on 1, 3, 5, 7 and 10 day after administration,rectal temperature per cow and somatic cell counts per quarter were recorded on 12 h, 3, 5, 7 and 10 day after administration, and pathogenic bacteria were isolated and identified on 10 day after administration. The data of rectal temperature, milk yield per day,somatic cell counts and pathogenic bacteria before and after administration were analyzed by SPSS software and the clinical symptom and adverse effects, such as red, swelling, heat and pain were observed continuously throughout the trial. 【Result】The average daily milk yield were 28.8, 27.7, 28.1, 28.7, 28.8, 29.2, and 29.6 kg on 1, 0 day before administration and 1, 3, 5, 7, and 10 day after administration, and it had no significant difference (P>0.05). The somatic cell counts per quarter at different time-points were all in the range of 300-500 thousand per milliliter. There were also no obvious difference in the average rectal temperature of 38.3, 38.4, 38.3, 38.3, 38.3, 38.2 and 38.3℃ at different time-points. The results for bacteria showed that totally 8 strains of E.coli, 5 strains of Streptococcus and 7 strains of Staphylococcus were isolated from the milk samples before administration, but only 1 strain of Streptococcus, 1 strain of Staphylococcus, and 1 strain of E.coli were isolated on 10 day after administration, and no new species of bacteria were found.【Conclusion】It was concluded that cefquinome sulfate intramammary infusion(Dry Cow) is safe for dairy cow, since it has no adverse effect on rectal temperature, milk yield and somatic cell counts.
cefquinome sulfate intramammary infusion; dry cow; safety; somatic cell counts
2016-03-15;接受日期:2016-06-14
國(guó)家重點(diǎn)研發(fā)計(jì)劃專項(xiàng)(2016YFD0501304)、農(nóng)業(yè)部公益性行業(yè)科研專項(xiàng)(201303038-3)、北京市農(nóng)業(yè)科技項(xiàng)目(20150146)、中國(guó)農(nóng)業(yè)科學(xué)院創(chuàng)新工程(FRI-06)、奶牛產(chǎn)業(yè)技術(shù)體系北京市創(chuàng)新團(tuán)隊(duì)專項(xiàng)
聯(lián)系方式:吳彤,E-mail:2715135608@qq.com。張道康,E-mail:zdkang619@163.com。吳彤和張道康為同等貢獻(xiàn)作者。通信作者劉義明,Tel:010-82106814;E-mail:liuyiming@caas.cn