Treatment of Prostatic Carcinoma with D-Trp-6-LH-RH: Plasma Hormone Levels After Daily Subcutaneous Injections and Periodic Administration of Delayed-Release Preparations

1986 ◽  
Vol 135 (3) ◽  
pp. 657-657
Author(s):  
M. Roger ◽  
J. Duchier ◽  
N. Lahlou ◽  
K. Nahoul ◽  
A.V. Schally
1986 ◽  
Vol 25 ◽  
pp. 137
Author(s):  
D. Gonzalez-Barcena ◽  
P.L. Perez ◽  
S N. Rangel ◽  
G H. Berea ◽  
A. Graef ◽  
...  

1992 ◽  
Vol 49 (3) ◽  
pp. 158-162 ◽  
Author(s):  
H. Fuse ◽  
S. Satomi ◽  
M. Okumura ◽  
T. Katayama

1981 ◽  
Author(s):  
Barnett Zumoff ◽  
David K. Fukushima ◽  
Robert S. Rosenfeld ◽  
Raymond G. Tropler ◽  
James Hickman

1997 ◽  
Vol 272 (6) ◽  
pp. E1130-E1135 ◽  
Author(s):  
G. D. Divertie ◽  
M. D. Jensen ◽  
P. E. Cryer ◽  
J. M. Miles

To determine whether the sensitivity of adipose tissue lipolysis to catecholamines is increased in poorly controlled insulin-dependent diabetes, the lipolytic response to epinephrine was measured in seven nondiabetic volunteers and seven poorly controlled diabetic subjects with use of [1-(14)C]palmitate as a tracer. Subjects received sequential 1-h infusions of epinephrine, which produced epinephrine concentrations of approximately 1,000, approximately 1,750, approximately 3,500, and approximately 6,000 pmol/l. A pancreatic clamp was used to maintain constant plasma hormone levels. Concentration-response curves were constructed for each subject from the integrated lipolytic response during each epinephrine infusion. There was no difference in maximal lipolytic response (117 +/- 19 vs. 152 +/- 11 mumol.kg-1.h-1) or in maximally effective (3,171 +/- 267 vs. 3,357 +/- 349 pmol/l) or half-maximally effective (1,081 +/- 109 vs. 1,015 +/- 120 pmol/l) epinephrine concentrations between nondiabetic and diabetic subjects, respectively (all P = NS). In control subjects, maximum beta-hydroxybutyrate concentrations were achieved at lower epinephrine concentrations than those required for a maximum lipolytic effect. Thus, under pancreatic clamp conditions, the lipolytic response to epinephrine in nondiabetic and diabetic subjects was similar.


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