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Benzothiadazine diuretics and death from myocardial infarction in hypertension. 苯并噻嗪利尿剂与高血压患者心肌梗死死亡。
Pub Date : 1978-12-01 DOI: 10.1042/cs055315s
J V Jones, F G Dunn, R Fife, A R Lorimer, R G Kellett

1. Case records were examined of 66 patients who died while being treated for high blood pressure. 2. The possibility that benzothiadazine diuretics may have some deleterious as well as beneficial effects was investigated. 3. It is possible that the thiazides may have some adverse clinical effects, at least in females, with regard to the incidence of myocardial infarction in hypertensive patients.

1. 研究人员检查了66名在接受高血压治疗期间死亡的患者的病例记录。2. 本研究探讨了苯并噻嗪类利尿剂可能既有有益作用又有有害作用的可能性。3.这是可能的噻嗪类药物可能有一些不利的临床效应,至少在女性中,关于高血压患者心肌梗死的发生率。
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引用次数: 18
Haemodynamic effects of a calcium antagonistic agent (nifedipine) in hypertension: therapeutic implications. 钙拮抗剂(硝苯地平)对高血压的血流动力学影响:治疗意义。
Pub Date : 1978-12-01 DOI: 10.1042/cs055291s
C Bartorelli, F Magrini, P Moruzzi, M T Olivari, A Polese, C Fiorentini, M Guazzi

1. In 27 severe primary hypertensive patients nifedipine (10 mg), administered orally, induced prompt (-21% of control at 30 min) and persistent (-17% at 120 min) fall of mean arterial pressure mediated through reduction of peripheral vascular resistance with rise of cardiac output. 2. The sublingual route (nine cases) showed more rapid onset of action and equal antihypertensive effectiveness. 3. In five patients with hypertensive crisis and acute left ventricular failure, the drug strikingly reduced systemic and pulmonary arterial pressures and relieved pulmonary oedema. 4. Prompt efficacy, ease of administration, absence of important side effects indicate that nifedipine may be a useful therapeutic agent in severe hypertension and in critical conditions that require rapid lowering of blood pressure.

1. 在27例重度原发性高血压患者中,口服硝苯地平(10 mg),通过降低外周血管阻力和心输出量的增加,诱导平均动脉压的迅速下降(30 min时为对照组的-21%)和持续下降(120 min时为-17%)。2. 舌下途径(9例)起效更快,降压效果相同。3.在5例高血压危象和急性左心室衰竭患者中,该药显著降低了全身和肺动脉压,减轻了肺水肿。4. 疗效迅速、给药方便、无重大副作用表明硝苯地平可能是严重高血压和需要快速降低血压的危重症患者的有效治疗药物。
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引用次数: 37
Assessment of early and delayed responses in vitamin B12 absorption during antibiotic therapy in tropical malabsorption. 热带吸收不良患者抗生素治疗期间维生素B12吸收早期和延迟反应的评估。
Pub Date : 1978-12-01 DOI: 10.1042/cs0550533
A M Tomkins, T Smith, S G Wright

1. Vitamin B12 absorption was measured in 18 patients with tropical malabsorption. 2. Absorption was particularly impaired in patients with severe mucosal lesions. 3. Sequential measurements with 57Co- and 58Co-labelled vitamin B12 were made before and 48 h after the start of tetracycline therapy. A rapid improvement (on average 22% increase in absorption) occurred in four of six patients with marked mucosal lesions. Further improvement occurred in four of five patients measured after 4 weeks' tetracycline, including the two who failed to improve initially. 4. These rapid changes in vitamin B12 absorption after antibiotics occur too early to be due to mucosal recovery and suggest that bacterial metabolism is an important factor in the malabsorption in these patients.

1. 对18例热带吸收不良患者的维生素B12吸收量进行了测定。2. 在严重粘膜病变的患者中,吸收特别受损。3.在四环素治疗开始前和48小时后,分别用57Co-和58co -标记的维生素B12进行顺序测量。6例有明显粘膜病变的患者中有4例出现快速改善(平均吸收量增加22%)。四环素治疗4周后,5名患者中有4名出现进一步改善,包括两名最初未能改善的患者。4. 抗生素后维生素B12吸收的这些快速变化发生得太早,不可能是由于粘膜恢复,这表明细菌代谢是这些患者吸收不良的重要因素。
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引用次数: 9
Acute effects of diuretics on potassium exchange, mechanical function and the action potential in rabbit myocardium. 利尿剂对兔心肌钾交换、机械功能及动作电位的急性影响。
Pub Date : 1978-12-01 DOI: 10.1042/cs0550555
P A Poole-Wilson, S M Cobbe, C H Fry

1. We have studied the acute effects of frusemide, triamterene and amiloride on potassium exchange, the action potential and mechanical function of isolated rabbit myocardium. 2. Potassium exchange in the myocardium was unaltered by these diuretics. 3. Frusemide and amiloride did not affect the action potential of rabbit papillary muscles. Triamterene caused a transient shortening of the action potential. 4. Frusemide and triamterene did not alter myocardial mechanical function in rabbit papillary muscles or the interventricular septum. Amiloride caused a reduction of about 5% in developed tension in two out of three papillary muscles.

1. 研究了氟塞米、曲氨蝶烯和阿米洛利对兔离体心肌钾交换、动作电位和力学功能的影响。2. 这些利尿剂未改变心肌钾交换。3.弗鲁塞米和阿米洛利对兔乳头肌的动作电位无影响。三苯胺引起动作电位的短暂缩短。4. 弗鲁塞米和曲氨蝶烯不改变兔乳头肌和室间隔的心肌力学功能。阿米洛利可使三分之二乳头肌的紧张程度降低约5%。
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引用次数: 11
The formation of tri-iodothyronine and reverse tri-iodothyronine from thyroxine in isolated rat renal tubules. 甲状腺素在离体大鼠肾小管中生成三碘甲状腺原氨酸和逆转三碘甲状腺原氨酸。
Pub Date : 1978-12-01 DOI: 10.1042/cs0550567
P Heyma, R G Larkins, J R Stockigt, D G Campbell

1. Conversion of thyroxine into tri-iodothyronine and reverse tri-iodothyronine in intact cells was studied with isolated renal tubules prepared by collagenase digestion. 2. Conversion of thyroxine into tri-iodothyronine and reverse tri-iodothyronine increased progressively for at least 90 min. 3. Studies of tri-iodothyronine production from increasing amounts of thyroxine revealed that the thyroxine to tri-iodothyronine conversion is saturable. 4. Iodine and carbimazole had no effect on the thyroxine to tri-iodothyronine conversion. 5. 6-Propyl-2-thiouracil had a direct non-competitive inhibitory effect on the conversion of thyroxine into tri-iodothyronine with a 75% inhibition of the conversion at a propylthiouracil concentration within the therapeutic range in vivo. Propylthiouracil also inhibited the net formation of reverse tri-iodothyronine from thyroxine at a similar propylthiouracil concentration, as well as inhibiting the subsequent degradation of reverse tri-iodothyronine.

1. 利用胶原酶消化制备的离体肾小管,研究了完整细胞中甲状腺素转化为三碘甲状腺原氨酸和逆转三碘甲状腺原氨酸的过程。2. 甲状腺素转化为三碘甲状腺原氨酸和逆转三碘甲状腺原氨酸的逐渐增加至少持续90分钟。从增加甲状腺素量产生三碘甲状腺原氨酸的研究表明,甲状腺素到三碘甲状腺原氨酸的转化是饱和的。4. 碘和卡咪唑对甲状腺素向三碘甲状腺原氨酸的转化没有影响。5. 6-丙基-2-硫脲嘧啶对甲状腺素转化为三碘甲状腺原氨酸具有直接的非竞争性抑制作用,在体内治疗范围内,丙基硫脲嘧啶浓度可抑制75%的转化。丙硫氧嘧啶还能抑制相似浓度丙硫氧嘧啶下甲状腺素净生成反三碘甲状腺原氨酸,并抑制反三碘甲状腺原氨酸随后的降解。
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引用次数: 18
Plasma noradrenaline and adrenaline and beta-adrenoreceptor responsiveness in renin subgroups of essential hypertension. 原发性高血压肾素亚组血浆去甲肾上腺素、肾上腺素和β -肾上腺素受体反应性。
Pub Date : 1978-12-01 DOI: 10.1042/cs055057s
F R Bühler, O Bertel, D W Kiowski
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引用次数: 13
Alterations of adrenal and uterine angiotensin II receptors during variation of sodium intake and/or experimental hypertension. 钠摄入量变化和/或实验性高血压时肾上腺和子宫血管紧张素II受体的改变
Pub Date : 1978-12-01 DOI: 10.1042/cs055171s
M A Devynck, M G Pernollet, G J Macdonald, P G Matthews, R S Raisman, P Meyer

1. Angiotensin II receptors from rat adrenal gland and myometrium were studied during variation of sodium intake. 2. In both target-tissues low Na+ diet increased the number of receptors whereas a high Na+ diet did not modify the adrenocortical receptors but increased the number of uterine receptors. 3. Deoxycorticosterone and one kidney Goldblatt hypertension were associated with a decrease in the number of adrenal receptors. 4. Alterations of angiotensin II receptors alone cannot explain satisfactorily the variations of sensitivity of target-cells to angiotensin II during sodium balance changes.

1. 研究了大鼠肾上腺和肌层血管紧张素受体在钠摄入量变化过程中的变化。2. 在两个靶组织中,低Na+饮食增加了受体的数量,而高Na+饮食没有改变肾上腺皮质受体,但增加了子宫受体的数量。3.脱氧皮质酮和单肾Goldblatt高血压与肾上腺受体数量减少有关。4. 单靠血管紧张素受体的改变并不能令人满意地解释钠平衡变化过程中靶细胞对血管紧张素II敏感性的变化。
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引用次数: 15
The fourth Volhard lecture: cardiovascular structural adaptation; its role in the initiation and maintenance of primary hypertension. 第四节沃尔哈德讲座:心血管结构适应;它在原发性高血压的发生和维持中的作用。
Pub Date : 1978-12-01 DOI: 10.1042/cs055003s
B Folkow
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引用次数: 444
Proceedings of the Fifth Meeting of the International Society of Hypertension, Paris, 12-14 June 1978. 国际高血压学会第五届会议论文集,巴黎,1978年6月12-14日。
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引用次数: 0
Plasma adrenaline and noradrenaline in essential hypertension and after long-term treatment with beta-adrenoreceptor-blocking agents. 血浆肾上腺素和去甲肾上腺素在原发性高血压和长期治疗后的β -肾上腺素受体阻滞剂。
Pub Date : 1978-12-01 DOI: 10.1042/cs055097s
R Franco-Morselli, M Baudouin-Legros, P Meyer

1. Plasma adrenaline and noradrenaline were measured in supine and upright positions in 27 essential hypertensive patients and in 12 age-matched control subjects. 2. Plasma adrenaline was markedly increased in a large proportion of patients, compared with control subjects, either in supine or in upright positions, whereas no significant differences were found in plasma noradrenaline. 3. Six hypertensive patients were chronically treated with beta-adrenoreceptor-blocking agents (five with propranolol and one with pindolol). Plasma noradrenaline was not significantly changed in the supine position but was markedly increased on standing in four out of six patients. Plasma adrenaline was decreased in five out of six patients either in suprine or upright positions. 4. These findings support the view that the adrenergic system participates in the mechanism of essential hypertension.

1. 对27例原发性高血压患者和12例年龄相匹配的对照组进行了仰卧位和直立位血浆肾上腺素和去甲肾上腺素的测定。2. 无论仰卧位还是直立位,与对照组相比,大部分患者血浆肾上腺素明显升高,而血浆去甲肾上腺素无显著差异。3.6例高血压患者长期应用β -肾上腺素受体阻滞剂治疗(5例应用心得安,1例应用品多洛尔)。平卧位时血浆去甲肾上腺素无明显变化,但站立位时血浆去甲肾上腺素明显升高。6例患者中有5例在仰卧位或直立位时血浆肾上腺素下降。4. 这些发现支持肾上腺素能系统参与原发性高血压发病机制的观点。
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引用次数: 22
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Clinical science and molecular medicine. Supplement
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