» Articles » PMID: 132978

Effect of Experimental Diabetes, Food Deprivation and Genetic Obesity on the Sensitivity of Pithed Rats to Autonomic Agents

Overview
Journal Br J Pharmacol
Publisher Wiley
Specialty Pharmacology
Date 1976 Jun 1
PMID 132978
Citations 14
Authors
Affiliations
Soon will be listed here.
Abstract

1 The sensitivities of alloxan and streptozotocin diabetic and hereditary obese pithed rats to acetylcholine, isoprenaline and noradrenaline were compared to those of controls. 2 Blood pressure and heart rate recordings made before dosing was started showed the streptozotocin-treated animals to have a significantly reduced heart rate and increased pulse pressure as compared with controls. 3 Both diabetic groups were found to have reduced sensitivities to the pressor effect of noradrenaline, the depressor effect of acetylcholine, the positive chronotropic and inotropic effect of isoprenaline and the reduction in diastolic pressure induced by isoprenaline. The reduction in sensitivity was generally much greater in the streptozotocin diabetic animals. 4 The genetically obese rats were found to have similar sensitivities to all three agents as did their non-obese litter mates. 5 When either diabetic group was deprived of food for 24 h preceding the tests the sensitivities were found to be raised significantly towards normal in almost all cases. 6 The results are contrasted with previous in vitro results and possible causative metabolic factors discussed. It is suggested that sensitivity changes are unevenly distributed within the cardiovascular system.

Citing Articles

Expression and Signaling of β-Adrenoceptor Subtypes in the Diabetic Heart.

Erdogan B, Michel M, Arioglu-Inan E Cells. 2020; 9(12).

PMID: 33256212 PMC: 7759850. DOI: 10.3390/cells9122548.


Parallel effects of β-adrenoceptor blockade on cardiac function and fatty acid oxidation in the diabetic heart: Confronting the maze.

Sharma V, McNeill J World J Cardiol. 2011; 3(9):281-302.

PMID: 21949571 PMC: 3176897. DOI: 10.4330/wjc.v3.i9.281.


Exercise training initiated after the onset of diabetes preserves myocardial function: effects on expression of beta-adrenoceptors.

Bidasee K, Zheng H, Shao C, Parbhu S, Rozanski G, Patel K J Appl Physiol (1985). 2008; 105(3):907-14.

PMID: 18583384 PMC: 2536823. DOI: 10.1152/japplphysiol.00103.2008.


Beneficial effect of the Ca2+ antagonist, nimodipine, on existing diabetic neuropathy in the BB/Wor rat.

Kappelle A, Biessels G, Bravenboer B, Van Buren T, Traber J, de Wildt D Br J Pharmacol. 1994; 111(3):887-93.

PMID: 8019766 PMC: 1910095. DOI: 10.1111/j.1476-5381.1994.tb14821.x.


The cardiac inotropic response to secretin is lower in genetically obese (fa/fa) than in lean (fa/?) Zucker rats.

Robberecht P, De Neef P, CAMUS J, Waelbroeck M, Fontaine J, Christophe J Pflugers Arch. 1983; 398(3):217-20.

PMID: 6314240 DOI: 10.1007/BF00657154.


References
1.
Richardson P, Withrington P . Proceedings: The effects of glucagon on the hepatic arterial vasculature of the dog: an inhibition of the effects of vasoconstrictor agents. Br J Pharmacol. 1975; 55(2):272P-273P. PMC: 1666769. View

2.
BRODY M, DIXON R . VASCULAR REACTIVITY IN EXPERIMENTAL DIABETES MELLITUS. Circ Res. 1964; 14:494-501. DOI: 10.1161/01.res.14.6.494. View

3.
Itaya K, Ui M . COLORIMETRIC DETERMINATION OF FREE FATTY ACIDS IN BIOLOGICAL FLUIDS. J Lipid Res. 1965; 6:16-20. View

4.
MANSFORD K, Opie L . Comparison of metabolic abnormalities in diabetes mellitus induced by streptozotocin or by alloxan. Lancet. 1968; 1(7544):670-1. DOI: 10.1016/s0140-6736(68)92103-x. View

5.
Kuntscherova J, VLK J . Influence of alloxan diabetes on acetylcholine synthesis in tissues of the albino rat. Physiol Bohemoslov. 1970; 19(5):431-4. View