組胺受體 的英文怎麼說
中文拼音 [zǔànshòutǐ]
組胺受體
英文
histamine receptors-
Conclusions the frequency of clinically important valve regurgitation was significantly increased in patients taking pergolide or cabergoline, but not in patients taking non ? ergot - derived dopamine agonists, as compared with control subjects
結論:與對照組相比,服用培高利特或者卡麥角林的患者臨床上發生重要瓣膜返流的頻率顯著增加,但服用非麥角?生的多巴胺受體激動劑的患者瓣膜返流的發生率卻未增加。Methods we performed an echocardiographic prevalence study in 155 patients taking dopamine agonists for parkinson ' s disease ( pergolide, 64 patients ; cabergoline, 49 ; and non ? ergot - derived dopamine agonists, 42 ) and 90 control subjects
方法:我們用超聲心動圖對155例正在服用多巴胺受體激動劑( 64例服用培高利特, 49例服用卡麥角林, 42例服用非麥角?生的多巴胺受體激動劑)治療帕金森病的患者和90例對照組進行了一項流行調查。Results clinically important regurgitation ( moderate to severe, grade 3 to 4 ) in any valve was found with significantly greater frequency in patients taking pergolide ( 23. 4 % ) or cabergoline ( 28. 6 % ) but not in patients taking non ? ergot - derived dopamine agonists ( 0 % ), as compared with control subjects ( 5. 6 % )
結果:與對照組相比( 5 . 6 % ) ,服用培高利特( 23 . 4 % )或者卡麥角林的患者( 28 . 6 % ) ,臨床上發生重要的任何瓣膜的返流(中到重度, 3級到4級)的頻率顯著升高,而服用非麥角?生的多巴胺受體激動劑的患者( 0 % )瓣膜返流的發生率卻未增加。Drug name diphenhydramine , ethanolamine class, histamine receptor type 1 blocker. has significant anticholinergic and sedative properties that causes some degree of topical anesthesia by impairing the transmission of nerve impulses
藥名:苯海拉明,氨基乙醇,組織胺受體1型阻滯劑有顯著的抗膽堿能和鎮靜特性,通過阻礙神經沖動傳導引起某種程度的局部麻醉。Role of central histamine injected intracerebroventricularly in etiologicalmechanism of neurogenic pulmonary edema in rabbits
家兔側腦室注射組胺受體拮抗劑對神經源性肺水腫的影響Slimming drugs commonly used appetite inhibitors, these drugs through the hypothalamus to influence diet and the central body of the excitement and inhibition play appetite, patients readily accept diet therapy, such as amphetamine - type ; metandienone increase metabolism, is to promote metabolism, so the body ' s adipose tissue accumulation by gradually eliminate, such as thyroid hormone ; biguanides hypoglycemic agents, the drugs in the treatment of diabetes, patients can cause loss of appetite, this is the side effects, but the drug has reduced the cumulative amount of fat and suppress appetite, delaying or reducing gastrointestinal absorption of the sugar, increase fecal fat and he substances excreted, speaking on obesity and is beneficial side
常用減肥藥物有食慾抑制劑,這類藥物是通過對下丘腦飲食中樞發生影響以及對全身的興奮而起到食慾抑制作用,使病人易於接受飲食療法,如苯丙胺類;增加代謝類藥,是促進機體代謝,使體內蓄積的脂肪組織逐漸消除,如甲狀腺激素;雙胍類降血糖藥,本類藥物在治療糖尿病時,可引起病人食欲不振,本是副作用,但此藥有降低脂肪積存量的作用,抑制食慾,延緩或減少胃腸道對糖分的吸收,增加糞便中脂肪及其他物質的排泄,對肥胖者來說恰是有利的一面。In this study, we use immunohistochemistry, electron microscope, cell culture, image analysis, mtt method and radioimmunoassay to study the localization, varies of quantitation, and possible frictions of 5 - ht and subtype of 5 - htr in human placenta. the results were as follows : 1
本研究用免疫組織化學、免疫電鏡、細胞培養、圖象分析、 mtt法和放射免疫等技術對5 -羥色胺及其受體亞型在胎盤絨毛中的細胞定位及對滋養層細胞增殖和激素分泌的影響進行了初步的探討,其結果如下: 1The relationship between the relative contents of 5 - hydroxytryptamime ( 5 - ht ) and its receptor and age in days of postnatal rat was studied by using immunohistchemistry and in situ quantitative analysis
為研究大鼠頜下腺5 -羥色胺及其受體的相對含量與日齡的關系,用免疫組織化學法結合原位定量,測定了大鼠頜下腺5 -羥色胺及其受體免疫反應產物的相對含量。It can be a side effect of drugs, from antihistamines to beta blockers. therefore, diagnosis can be tricky and time - consuming
它可能是藥物的副作用,是抗組織胺類藥或? -受體阻滯藥所引起的。因此,診斷是棘手的,也是耗費時間的。In this experiment hcv structural gene was amplified by polymerase chain reaction ( pcr ), and was inserted into baculovirus expression vector pfastbacl to construct a recombinant transposing vector pfbl - cee. the plasmid pfb 1 - cee was transformed into dh1 obac competent e. coli cells. high molecular weight dna was prepared from the overnight cultures from the selected e. coli colonies, which was recombinant baculovirus shuttle vector containing hcv structural gene, named bac - cee
本實驗用pcr擴增hcv結構區基因,克隆到桿狀病毒表達載體pfastbacl中,構建成重組轉座載體pfb1 - cee ,轉化dh10bac大腸桿菌感受態細胞,篩選陽性菌落,抽提大分子質粒dna ,獲得含hcv結構區基因的重組桿狀病毒穿梭載體bac - cee ,脂質體介導轉染sf9昆蟲細胞,出現細胞病變后,收集含有重組桿狀病毒顆粒的培養上消,重新感染sf9細胞,收集sf9細胞,進行12 . 5 sds -聚丙烯酰胺凝膠電泳,可見表達的蛋白條帶。To confirm that the histamine receptor connects the drug, ampk activity and appetite, the team gave clozapine to mice genetically engineered without a histamine receptor
為證實組胺受體和藥物、 ampk活性、和食慾相關,研究組給經遺傳重組后缺失去組胺受體的小鼠氯氮平藥物。Incyte does not actually own the rights to the gene for the histamine receptor in your body but only to an “ isolated and purified ” form of it. ( at times, patent examiners or courts have invoked the u. s
早期的基因專利還依循傳統化學專利的模式,例如因賽特公司並不是真的擁有你體內的組織胺受體基因,而是分離和純化形式的基因(當時專利審核人員或法院還引用了美國憲法中禁止奴役的條文,解釋為什麼不能申請一個真正的人或其身體部位的專利權) 。分享友人