2016
DOI: 10.1016/s0168-8278(16)00739-x
|View full text |Cite
|
Sign up to set email alerts
|

Noradrenaline Potentiates Portal Hypertension through the Alpha 2a Adrenergic Receptor – A target for Therapy in Portal Hypertension

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1

Citation Types

0
2
0
1

Year Published

2017
2017
2022
2022

Publication Types

Select...
3

Relationship

0
3

Authors

Journals

citations
Cited by 3 publications
(3 citation statements)
references
References 0 publications
0
2
0
1
Order By: Relevance
“…Moreover, in vitro studies demonstrated that portal vein myocytes in rats and strips of the canine portal vein in dogs contract in response to exposure to alpha 2 adrenergic agonists 22,23 . This may lead to a transient increase in intrahepatic portal vascular resistance and temporary portal hypertension, 24 which has been previously associated with gallbladder wall thickening in humans 25 . This theory is supported by a prior study that demonstrated reduced portal vein velocity as measured ultrasonographically following the administration of dexmedetomidine, producing velocities consistent with portal hypertension 11 .…”
Section: Discussionmentioning
confidence: 99%
“…Moreover, in vitro studies demonstrated that portal vein myocytes in rats and strips of the canine portal vein in dogs contract in response to exposure to alpha 2 adrenergic agonists 22,23 . This may lead to a transient increase in intrahepatic portal vascular resistance and temporary portal hypertension, 24 which has been previously associated with gallbladder wall thickening in humans 25 . This theory is supported by a prior study that demonstrated reduced portal vein velocity as measured ultrasonographically following the administration of dexmedetomidine, producing velocities consistent with portal hypertension 11 .…”
Section: Discussionmentioning
confidence: 99%
“…Недавно опубликованы результаты применения при экспериментальном холестатическом циррозе нового α2-адреноблокатора BRL44408, который эффективно снижал уровень ПД и не оказывал значительного влияния на системную гемодинамику. Однако данный эффект до настоящего времени получен только на крысах [11,12].…”
Section: результаты и обсуждениеunclassified
“…In experimental cholestatic cirrhosis, short-term therapy with the α2 antagonist BRL44408 significantly decreased portal pressure and did not alter systemic haemodynamics even without NSBB cotherapy, which, however, has been published in only two abstracts so far [ 12 , 13 ].…”
Section: Adrenoceptor Drugsmentioning
confidence: 99%