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- Amlodipine(ALDP) is a new kind of calcium channel blocker of dihydropyridine. 氨氯地平是新型二氫吡啶類(lèi)鈣通道阻滯劑。
- The calcium channel blocker had similar effect and was concerned by doctors. 而鈣通道阻滯劑治療消化性潰瘍的療效已引起廣大醫生的關(guān)注。
- Methods: Whole-cell patch clamp technique was used to determine sodium channel cur rent. 方法 :采用全細胞膜片鉗技術(shù) ,記錄鈉通道電流。
- Bepridil (Bep), an Ca 2+ channel blocker, ip 5 mg/kg 30 min prior to hypoxia served as positive control. 并以芐普地爾 5 m g/ kg ip給藥作陽(yáng)性對照。
- Sodium channel of dorsal root ganglion (DRG) plays an important role in the mechanisms of neuropathic pain. 摘要脊髓背根神經(jīng)節的鈉通道與神經(jīng)性疼痛的形成有密切的關(guān)系。
- Conclusions:Coronary spasm can provoke lethal arrhythmia,but be tr eated effectively with Calcium Channel Blocker. 結論：冠狀動(dòng)脈痙攣可誘發(fā)嚴重的心律失常，鈣拮抗劑治療有效。
- Tetrodotoxin is one of the strong marine neural toxins which block sodium channels. 河豚毒素是鈉離子通道阻斷劑,是一種強海洋神經(jīng)毒劑。
- These anaesthetics block sodium channels and thereby the excitability of all neurons, not just sensory neurons. 這些局麻劑可以阻斷鈉通道，因此不僅僅阻滯了感覺(jué)神經(jīng)元，也同時(shí)阻滯了幾乎所有其他神經(jīng)元的興奮性。
- The results suggest that RSM may be a kind of selective slow calcium channel blocker and able to prevent myocardium from injury of ISO. 提示:丹參可能為鈣桔抗劑,并能對抗ISO引起的心肌鈣超載性損傷。
- This review focuses on the relationship between the plasticity of voltage-gated sodium channel subunits and neuropathic pain states. 本文就目前研究較多的幾種鈉通道亞單位的可塑性與神經(jīng)性疼痛的關(guān)系作一綜述。
- The mechanism of treating traumatic cerebral edema with calcium channel blocker is to inhibit EAA releasing and to inhibit Ca 2+ influx directly. 鈣通道阻斷劑治療外傷性腦水腫的機制是抑制腦外傷后EAA釋放及直接減少Ca2＋內流。
- It can activate sodium channel,inrease sodium current.it can inrease liber calcium concentration in the myocardial cell. 實(shí)驗證明：As可激活鈣通道，增加鈣通道電流 As增加細胞內游離的鈣離子濃度 As可激活鈉通道，增加鈉電流 關(guān)鍵詞：龍牙蔥木皂苷 培養心肌細胞 L-型鈣電流 鈉通道 膜片鉗 正性肌力作用 Aralosides(As)are omni-glycosides extracted from roots;petiols and skins of Aralia (Miq) seem.
- AIM: To investigate the effects of nifedipine, a calcium channel blocker, on cellular proliferation of gingival fibroblasts in vitro . 目的:探討鈣拮抗劑硝苯地平對牙齦成纖維細胞的作用。
- These included mutations in the sodium channel gene SCN5A, preiously associated with LQTS and other unstable heart rhythm conditions and sudden death. 這其中包括鈉通道基因SCN5A的突變，該基因以前發(fā)現與LQTS、其他不穩定心律失常以及猝死相關(guān)。
- Nifedipine (nifedipine) is the last century in the early 70 listed a calcium channel blocker treatment of cardiovascular disease category. 硝苯地平（心痛定）是上世紀70年代初上市的一種鈣通道拮抗劑類(lèi)心血管病治療藥物。
- They are lipophilic, so can enter virtually any neuron, where they indiscriminately block sodium channels in the membrane. 它們的親油性使它們能進(jìn)入幾乎任何神經(jīng)元，在那里，它們會(huì )不加甄別地阻斷細胞膜中的鈉通道。
- CONCLUSION GLB used as KATP channel blocker can reduce the extent of augmentation of TDR in the initial stage when coronary artery was ligated. 結論使用KATP通道阻斷劑GLB可減小冠脈結扎后初期心室肌TDR增大程度。
- The voltage gated sodium channel is the major target receptor for DDT and pyrethroids, and is the basis of their cross resistance (knockdown resistance). 電壓門(mén)控的鈉通道是擬除蟲(chóng)菊酯 (Pyrethroid)和滴滴涕 (dichloro diphenyl trichloroethane)的共同靶變點(diǎn) ,是它們產(chǎn)生交互抗性 (擊倒抗性 ,Knockdownresistance)的基礎。
- Effects of neuromuscular blocker (NMB) of atracurium (ATC) and vecuronium (VCR ) in patients on calcium - channel blocker(CCB), nifedipine, therapy were studied with Accelograph. 觀(guān)察了鈣通道阻滯藥（CCB）硝苯吡啶（Nif）與阿屈可林（ATC）或維庫溴銨（VCR）聯(lián)用對患者神經(jīng)肌肉阻滯（NMB）效應的影響。
- To observe the effect of Garlicin on sodium channel in isolated ventricular cell of rats, to find out the mechanism of antiarrhythmia of Garlicin on the ionic channel level. 目的研究大蒜素對豚鼠心室肌細胞膜快鈉通道的影響,探討大蒜素在離子通道水平的抗心律失常作用機制。
