鈣通道 的英文怎麼說

中文拼音 [gàitōngdào]
鈣通道 英文
calcium cha el
  • : 名詞[化學] calcium (20號元素, 符號 ca)
  • : 通量詞(用於動作)
  • : Ⅰ名詞(道路) road; way; route; path 2 (水流通過的途徑) channel; course 3 (方向; 方法; 道理) ...
  • 通道 : thoroughfare; passageway; pass; enterclose; gallery; drong; tunnel; avenue; alure; way; row; key ...
  1. Preliminary study on calcium channel blocking effects of 5 chinese herbs

    五種中草藥對鈣通道阻滯作用的初步研究
  2. Two types of nondepolarizing - activated calcium channels on the spinal cholinergic neurons from embrynoic xenopus laevis

    爪蟾胚胎脊髓膽堿能神經元上兩類非去極化激活的鈣通道
  3. Intracellular calcium channels : cadpr modulated ryanodine receptors

    細胞內鈣通道
  4. This experiment was performed using the " yingqing " peach fruit and " chunxing " strawberry to study the changes of the main physiology - biochemistry characteristics and the microsome membrane ca + - atpase activities during the fruits ripening. the effects of ethylene, trifluoperizine ( tfp ) + ethylene and verapamil ( ver ) + ethylene treatments on the above changes were discussed. the objects of the thesis may further explore the role of calcium messenger in the ethylene signal transduction, and provide some new theoretical basis for further research of the microsome membrane ca2 + - atpase during the fruits ripening

    本論文以迎慶桃和春星草莓為試材,研究了兩類果實采后在25和4條件下主要生理生化變化和ca ~ ( 2 + ) - atpase活性變化以及乙烯、調素拮抗劑tfp +乙烯和鈣通道阻塞劑ver +乙烯處理對其的影響,為探討果實成熟衰老過程中,信使系統在乙烯信號轉導中的作用,提供一定的理論依據,並為探索ca ~ ( 2 + ) - atpase在果實衰老中的作用及作用機制,提供實驗證據。
  5. So far, six kinds of medicines are authorised to be applied to the treatment of hypertension by the world health organization ( who ), including diuretics, - receptor blocking agent, - receptor blocking agent, angiotensin receptor antagon, calcium channal blocking agent and angiotensin converting enzyme inhibitors ( aceis )

    目前,世界衛生組織( who )批準用於治療高血壓病的一線藥物主要有利尿劑、受體阻斷劑、血管緊張素轉換酶抑制劑( acei ) 、鈣通道阻滯劑( caa ) 、受體阻斷劑、血管緊張素( ang )受體拮抗劑等六大類。
  6. The purposes of the present study were to investigate ( 1 ) the hemodynamic effects of agmatine in anaesthetized dahl salt - sensitive ( ds ) hypertensive and dahl salt - resistant ( dr ) rats ; ( 2 ) the effect of agmatine on vascular tension in the isolated aortic artery of rats and the underlying receptor mechanism ; ( 3 ) the effects of local injection of agmatine on femoral, renal, and mesenteric vascular beds by constant flow perfusion method ; ( 4 ) the effect of agmatine on l - type calcium current ( / ca - t ) in rat ventricular myocytes with whole - cell configuration of the patch - clamp technique ; ( 5 ) the effects of agmatine on free intracellular calcium concentration ( ca2 + d of isolated rat ventricular myocytes

    ( 3 )採用後肢、腎臟和腸系膜動脈在體恆流灌注法,觀察向灌流環路中直接注射胍丁胺的血管效應。 ( 4 )應用全細胞膜片箝技術,觀察胍丁胺對大鼠心室肌細胞l -型鈣通道電流( i _ ( ca - l ) )的影響。 ( 5 )用fluo3 - am負載分離的大鼠心室肌細胞后,由激光共聚焦法測定單個心室肌細胞[ ca ~ ( 2 + ) ] _ i的熒光強度,觀察胍丁胺對分離大鼠心室肌細胞內游離濃度( [ ca ~ ( 2 + ) ] _ i )的影響。
  7. On the other hand, angiotensin converting enzyme inhibitors may be more suitable in a yin deficiency and yang hyperactivity pattern as well as combined liver and kidney yin deficiency pattern

    鈣通道阻滯劑對血脈瘀阻型、痰濕壅型高血壓,受體阻滯劑對于肝陽上亢型高血壓,血管緊張素轉換酶抑制劑對陰虛陽亢型或肝腎陰虛型高血壓療效較好的機制還有待研究。
  8. ( 2 ) in high ca2 + krebs - henseleit ( k - h ) solution ( twice of normal concentration ), duration of phasic contraction induced by fac was prolonged, which was longer than 60min, and the contractile amplitude was enhanced to 58. 71 ?. 71 % ( p < 0. 01 ). after rings were incubated with nifedipine for 15min in order to block the l - type ca2 + channel, the iron induced contractile amplitude was inhibited

    主動脈環用硝苯毗吒( nifedpine , nif )孵育15min以阻斷卜型鈣通道后,再給予鐵刺檄,與未加nif的同濃度細胞外離于組相比,鐵所致的收縮幅度均明顯降低(均p 0刀1 ) ,且高液中鐵引起的相位性收縮幅度明顯高於正常組。
  9. Ccbs calcium channel blockers

    鈣通道抑制劑
  10. Among patients with the metabolic syndrome ( 7, 327 black and 15, 750 white patients ), the calcium channel blocker, ace inhibitor and alpha - blocker had higher rates of heart failure compared with the diuretic ; the ace inhibitor and the alpha - blocker also had an increased risk of combined cardiovascular disease

    在合併代謝綜合徵人群(黑種人7327名白種人15750名)中,鈣通道阻滯劑、血管緊張素轉換酶抑制劑-阻滯劑治療組較利尿劑治療組有更高的心衰發病率; -阻滯劑治療組、血管緊張素轉換酶抑制劑治療組也有並發心血管疾病的危險性增高。
  11. Intracellular calcium channels : naadp modulated

    細胞內鈣通道
  12. Voltage dependent channel, vdc

    電壓依賴性鈣通道
  13. Calcium channel blockers for irritable bowel syndrome : systematic review

    選擇性鈣通道拮抗劑治療腸易激綜合征的系統評價
  14. Effect of herba epimedii on the visceral organs and myocardial ischemia injury in rats

    鈣通道及其心肌缺血性損傷的影響
  15. Vascular and biological characteristics of amlodipine beyond l - type calcium antagonist

    鈣通道阻滯作用以外的血管生物學特性
  16. The effect of ca2 channel bloker on insulin secretion in rat pancreatic islet cells

    鈣通道拮抗劑對大鼠胰島細胞胰島素分泌的影響
  17. The main physiology - biochemistry changes were determined in the two fruits after treating with trifluoperizine, a caimodulin antagnist, and verapamil, a calcium channel blocker. the results showed that trifluoperizine and verapamil weakened the effects of the exogenous ethylene on the the main physiology - biochemistry

    調素拮抗劑tfp和鈣通道阻塞劑ver抑制了外源乙烯促進果實衰老時的乙烯釋放量、 o _ ~ -的積累和膜脂過氧化產物mda的增加。
  18. 5 - ht induced local ca 2 + transients ( ca2 + sparks ) in cultured rat stomach fundus smooth muscle cells ( sfsmc ) was first observed by using the new fluorescent ca2 + indicator stdin and laser scanning confocal microscope. the mechanisms of initiation of ca2 + sparks and propagating ca2 + waves and their relation to e - c coupling were also discussed. 4. the effects of reactive oxygen species on the spectral properties of the new fluorescent ca2 + indicator stdin were evaluated using four different oxidant - generating systems

    應用於5一ht誘導胃底平滑肌細胞胞內游離ca2 +動員的機制研究,發現5一ht過促進外內流和內釋放使[ caz + j升高;在胃底平滑肌5一ht升高ca , 『 ,系過5一htz受體介導的1p3 / ca , 『和dg / pkc雙信使途徑; 5一ht過l型鈣通道促進外內流。
  19. The effects of naloxone on neuron apoptosis in cerebral ischemic tissue of wistar rats after focal cerebral ischemia - reperfusion injury

    粉防己堿對缺氧所致大鼠皮層神經元鈣通道功能變化的影響
  20. With holding potential of - - 80 mv depolarization beyond - - 50 mv elicited an inward current, peaked at + l0mv and reversed between + 40 mv and + 60 mv 5 ll m nicardipine, a potent blocker of l - type calcium channel, markedly blocked the " ib

    開始出現,峰值在去極化刺激至10 20mv出現,翻轉電位為巧0仍0mv 。 l型鈣通道特異性阻斷劑nicadipine可以明顯抑制ib 。 ,並且iv曲線分佈在應用nicardipine前後無改受。
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