Interaction of clonidine with chronotropic agents on isolated right atria

1980 ◽  
Vol 58 (1) ◽  
pp. 28-33 ◽  
Author(s):  
Robert L. Rodgers ◽  
Thomas E. Tenner Jr. ◽  
Ismail E. Laher ◽  
John H. McNeill

Clonidine was administered to isolated guinea pig right atria in order to characterize its chronotropic activity and its interaction with other chronotropic agents at the postjunctional level. Clonidine either had no significant effect (10−7–10−4 M) or decreased (10−3 M) atrial rate. Pretreatment of the atria with clonidine noncompetitively antagonized (10−6–10−4 M) the positive chronotropic actions of isoproterenol, and competitively antagonized (10−4 M) the negative chronotropic actions of pilocarpine. At doses of 10−6 or 3 × 10−6 M, clonidine also noncompetitively antagonized the positive chronotropic effects of 4-methylhistamine and glucagon. The results show that clonidine antagonizes both adrenergic and cholinergic influences on atrial rate at the postjunctional level and suggest that the antagonism of adrenergic influences does not involve a direct interaction with β-adrenergic receptors.


1980 ◽  
Vol 58 (2) ◽  
pp. 167-173 ◽  
Author(s):  
Campbell Wilson ◽  
Kenneth J. Broadley

The positive chronotropic responses of guinea pig isolated right atria to histamine were antagonized by metiamide (pA2, 5.95) thus confirming their H2 receptor classification. The positive inotropic responses of paced left atria were antagonized to some extent by mepyramine to give a pA2 value of 7.87, indicating the involvement of H1 receptors. A limit to the shift of cumulative dose–response curves for the inotropic response suggested an H1 receptor resistant component. The inotropic response to sequentially administered histamine was biphasic. On lowering the temperature to 25 °C, the two components became more demarcated and separated by a negative phase. Only the primary positive component and the negative component were antagonized by mepyramine. At 38 °C, the response was similarly converted to a monophasic one. The residual responses were resistant to metiamide and propranolol antagonism and therefore not mediated via H1, H2, or β-adrenergic receptors.



1989 ◽  
Vol 160 (3) ◽  
pp. 751-757 ◽  
Author(s):  
Christos G. Hatjis ◽  
Donald R. Koritnik ◽  
David M. Grogan


1986 ◽  
Vol 111 (2) ◽  
pp. 263-270 ◽  
Author(s):  
J. M. Fyles ◽  
M. A. Cawthorne ◽  
S. L. Howell

ABSTRACT The sympathetic nervous system is believed to play a part in the control of insulin release from the pancreatic islets of Langerhans. Stimulation of α-adrenoceptors is thought to inhibit the release of insulin whereas stimulation of β-adrenoceptors enhances insulin release. The present experiments were conducted to establish the existence of β-adrenergic receptors on guinea-pig and rat islet cells and to quantify them using the selective β-adrenergic ligands [3H]dihydroalprenolol (DHA) and [125I]cyanoiodopindolol (CYP). Guinea-pig islets had 62 fmol β-adrenoceptors/mg protein using [3H]DHA, corresponding to 43 700 binding sites/cell and 25 fmol β-adrenoceptors/mg protein using [125I]CYP, corresponding to 17 400 sites/cell. Rat islet cells were found to have 4·6 fmol β-adrenoceptors/mg protein using [125I]CYP, corresponding to 7200 sites/cell. Adenylate cyclase activation exhibited a positive dose–response relationship when exposed to the β-adrenoceptor agonist isoprenaline, with a maximum response (190 ± 21% above basal) at 10 μmol isoprenaline/l. This response was abolished with 1 μmol/l of the β-adrenergic antagonist 1-alprenolol. Insulin secretion in the presence of 10 mmol glucose/l, but in the absence of the α-adrenoceptor blocker phentolamine, was not affected by 10 μmol isoprenaline/l. However, perifusion experiments showed that secretion of insulin from isolated rat islets in the presence of 10 mmol glucose/l was significantly increased (332%) by 10 μmol isoprenaline/l in the presence of 10 μmol phentolamine/l. These results suggest that binding of selective radio-labelled ligands occurs to β-adrenergic receptors on the B cell surface of the islets of Langerhans, and that these receptors are functionally coupled to insulin secretion through modulation of adenylate cyclase activity. J. Endocr. (1986) 111, 263–270



1997 ◽  
Vol 11 (2) ◽  
pp. 111-116 ◽  
Author(s):  
D. Scherrer ◽  
E. Lach ◽  
Y. Landry ◽  
JP Gies


2016 ◽  
Vol 30 (22) ◽  
pp. 2605-2610 ◽  
Author(s):  
Luiz Henrique Agra Cavalcante-Silva ◽  
Ana Carolina de Carvalho Correia ◽  
Jéssica Celestino Ferreira Sousa ◽  
José Maria Barbosa-Filho ◽  
Bárbara Viviana de Oliveira Santos ◽  
...  


1984 ◽  
Vol 62 (1) ◽  
pp. 23-26 ◽  
Author(s):  
Jamshid Latifpour ◽  
John H. McNeill

Using radioligand binding techniques, the effect of reserpine pretreatment on ventricular adrenergic receptors from guinea pig was studied. [3H]Prazosin and [3H]dihydroalprenolol were used to label α1- and β-adrenergic receptors, respectively. Administration of 2.5 mg/kg reserpine for 2 days caused a significant increase in the number of β-adrenergic receptors with no effect on their affinity to respective ligands. Similar reserpine pretreatment did not affect either density or affinity of α1-adrenergic receptors for ligands. The results may explain the previous report from our laboratory in which an identical reserpine pretreatment selectively enhanced the inotropic responsiveness of the working guinea pig heart to isoproterenol.



1971 ◽  
Vol 246 (9) ◽  
pp. 3037-3041
Author(s):  
Mark Chasin ◽  
I. Rivkin ◽  
Frank Mamrak ◽  
S.G. Samaniego ◽  
S.M. Hess


Sign in / Sign up

Export Citation Format

Share Document