Haemodynamic determinants of the arterial blood pressure rise during growth in conscious puppies

1978 ◽  
Vol 12 (7) ◽  
pp. 422-428 ◽  
Author(s):  
F. MAGRINI
1962 ◽  
Vol 17 (6) ◽  
pp. 938-942 ◽  
Author(s):  
C. Robert Olsen ◽  
Darrell D. Fanestil ◽  
Per F. Scholander

Five men of outstanding diving ability performed apneic underwater dives in a specially fitted tank. The divers hyperventilated to extreme degrees of hypocapnia before submerging, and their arterial blood carbon dioxide tensions rarely rose above normal levels during a dive. Arterial blood oxygen content was 15.5 vol % or above at the end of two 3-min resting dives and of three 1.5-min exercise dives. Blood lactate concentrations increased during the latter half of exercise dives and reached peak values after surfacing. A rise in arterial blood pressure began by 10 sec in each dive and persisted, coincident with a falling heart rate, to the end of the dive. The rate of blood pressure rise was greater during a dive in water of 26 C than with breath holding by the same subject out of water. Some differences between the adaptations of diving men and of other diving mammals are briefly discussed. Submitted on April 2, 196


1973 ◽  
Vol 45 (s1) ◽  
pp. 181s-183s
Author(s):  
Lennart Hansson ◽  
Stephen N. Hunyor

1. Clonidine was withdrawn acutely in five hypertensive patients with a documented blood pressure over-shoot after previous temporary cessation of treatment. 2. In all patients a severe rise of systolic and diastolic blood pressure was seen (average 67/58 mmHg). This was accompanied by a number of ‘withdrawal symptoms’, e.g. restlessness, tremor, headaches and nausea. 3. Catecholamines in urine rose from 32 μg/l to 112 μg/l (001 < P < 0.02) and in arterial blood from 0.52 μg/l to 1.0 μg/l (not significant). 4. The crisis could be reversed acutely by α- and β-adrenergic blockade. 5. Catecholamine depletion with reserpine before the withdrawal of clonidine seemed to reduce the blood pressure rise and the withdrawal symptoms.


2020 ◽  
Vol 20 (8) ◽  
pp. 1253-1261
Author(s):  
Mourad Akdad ◽  
Mohamed Eddouks

Aims: The present study was performed in order to analyze the antihypertensive activity of Micromeria graeca (L.) Benth. ex Rchb. Background: Micromeria graeca (L.) Benth. ex Rchb is an aromatic and medicinal plant belonging to the Lamiaceae family. This herb is used to treat various pathologies such as cardiovascular disorders. Meanwhile, its pharmacological effects on the cardiovascular system have not been studied. Objective: The present study aimed to evaluate the effect of aqueous extract of aerial parts of Micromeria graeca (AEMG) on the cardiovascular system in normotensive and hypertensive rats. Methods: In this study, the cardiovascular effect of AEMG was evaluated using in vivo and in vitro investigations. In order to assess the acute effect of AEMG on the cardiovascular system, anesthetized L-NAME-hypertensive and normotensive rats received AEMG (100 mg/kg) orally and arterial blood pressure parameters were monitored during six hours. In the sub-chronic study, rats were orally treated for one week, followed by blood pressure assessment during one week of treatment. Blood pressure was measured using a tail-cuff and a computer-assisted monitoring device. In the second experiment, isolated rat aortic ring pre-contracted with Epinephrine (EP) or KCl was used to assess the vasorelaxant effect of AEMG. Results: Oral administration of AEMG (100 mg/kg) provoked a decrease of arterial blood pressure parameters in hypertensive rats. In addition, AEMG induced a vasorelaxant effect in thoracic aortic rings pre-contracted with EP (10 μM) or KCl (80 mM). This effect was attenuated in the presence of propranolol and methylene blue. While in the presence of glibenclamide, L-NAME, nifedipine or Indomethacin, the vasorelaxant effect was not affected. Conclusion: This study showed that Micromeria graeca possesses a potent antihypertensive effect and relaxes the vascular smooth muscle through β-adrenergic and cGMP pathways.


1946 ◽  
Vol 146 (3) ◽  
pp. 410-421 ◽  
Author(s):  
J. P. Holt ◽  
W. J. Rashkind ◽  
R. Bernstein ◽  
J. C. Greisen

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