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Dipeptidyl Peptidase‐4 Inhibition Potentiates Stimulated Growth Hormone Secretion and Vasodilation in Women
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Background
Diminished growth hormone (
GH
) is associated with impaired endothelial function and fibrinolysis.
GH
‐releasing hormone is the primary stimulus for
GH
secretion and a substrate of dipeptidyl peptidase‐4. We tested the hypothesis that dipeptidyl peptidase‐4 inhibition with sitagliptin increases stimulated
GH
secretion, vasodilation, and tissue plasminogen activator (
tPA
) activity.
Methods and Results
Healthy adults participated in a 2‐part double‐blind, randomized, placebo‐controlled, crossover study. First, 39 patients (29 women) received sitagliptin or placebo on each of 2 days separated by a washout. One hour after study drug, blood was sampled and then arginine (30 g IV) was given to stimulate
GH
. Vasodilation was assessed by plethysmography and blood sampled for 150 minutes. Following a washout, 19 of the original 29 women received sitagliptin alone versus sitagliptin plus antagonist to delineate
GH
receptor (
GHR
)– (n=5), nitric oxide– (n=7), or glucagon‐like peptide‐1 receptor– (n=7) dependent effects. Sitagliptin enhanced stimulated
GH
secretion (
P
<0.01 versus placebo, for 30 minutes) and free insulin–like growth factor‐1 (
P
<0.001 versus placebo, after adjustment for baseline) in women. Vasodilation and
tPA
increased in all patients, but sitagliptin enhanced vasodilation (
P
=0.01 versus placebo) and increased
tPA
(
P
<0.001) in women only.
GHR
blockade decreased free insulin–like growth factor‐1 (
P
=0.04 versus sitagliptin alone) and increased stimulated
GH
(
P
<0.01), but decreased vascular resistance (
P
=0.01) such that nadir vascular resistance correlated inversely with
GH
(
r
s
=−0.90,
P
<0.001).
GHR
blockade suppressed
tPA
. Neither nitric oxide nor glucagon‐like peptide‐1 receptor blockade affected vasodilation or
tPA
.
Conclusions
Sitagliptin enhances stimulated
GH
, vasodilation, and fibrinolysis in women. During sitagliptin, increases in free insulin–like growth factor‐1 and
tPA
occur via the
GHR
, whereas vasodilation correlates with
GH
but occurs through a
GHR
‐independent mechanism.
Clinical Trial Registration
URL
:
http://www.clinicaltrials.gov
. Unique identifier:
NCT
01701973.
Ovid Technologies (Wolters Kluwer Health)
Title: Dipeptidyl Peptidase‐4 Inhibition Potentiates Stimulated Growth Hormone Secretion and Vasodilation in Women
Description:
Background
Diminished growth hormone (
GH
) is associated with impaired endothelial function and fibrinolysis.
GH
‐releasing hormone is the primary stimulus for
GH
secretion and a substrate of dipeptidyl peptidase‐4.
We tested the hypothesis that dipeptidyl peptidase‐4 inhibition with sitagliptin increases stimulated
GH
secretion, vasodilation, and tissue plasminogen activator (
tPA
) activity.
Methods and Results
Healthy adults participated in a 2‐part double‐blind, randomized, placebo‐controlled, crossover study.
First, 39 patients (29 women) received sitagliptin or placebo on each of 2 days separated by a washout.
One hour after study drug, blood was sampled and then arginine (30 g IV) was given to stimulate
GH
.
Vasodilation was assessed by plethysmography and blood sampled for 150 minutes.
Following a washout, 19 of the original 29 women received sitagliptin alone versus sitagliptin plus antagonist to delineate
GH
receptor (
GHR
)– (n=5), nitric oxide– (n=7), or glucagon‐like peptide‐1 receptor– (n=7) dependent effects.
Sitagliptin enhanced stimulated
GH
secretion (
P
<0.
01 versus placebo, for 30 minutes) and free insulin–like growth factor‐1 (
P
<0.
001 versus placebo, after adjustment for baseline) in women.
Vasodilation and
tPA
increased in all patients, but sitagliptin enhanced vasodilation (
P
=0.
01 versus placebo) and increased
tPA
(
P
<0.
001) in women only.
GHR
blockade decreased free insulin–like growth factor‐1 (
P
=0.
04 versus sitagliptin alone) and increased stimulated
GH
(
P
<0.
01), but decreased vascular resistance (
P
=0.
01) such that nadir vascular resistance correlated inversely with
GH
(
r
s
=−0.
90,
P
<0.
001).
GHR
blockade suppressed
tPA
.
Neither nitric oxide nor glucagon‐like peptide‐1 receptor blockade affected vasodilation or
tPA
.
Conclusions
Sitagliptin enhances stimulated
GH
, vasodilation, and fibrinolysis in women.
During sitagliptin, increases in free insulin–like growth factor‐1 and
tPA
occur via the
GHR
, whereas vasodilation correlates with
GH
but occurs through a
GHR
‐independent mechanism.
Clinical Trial Registration
URL
:
http://www.
clinicaltrials.
gov
.
Unique identifier:
NCT
01701973.
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