Literature DB >> 1340060

Receptor strategies in pancreatitis.

J H Grendell1.   

Abstract

A variety of receptors on pancreatic acinar and duct cells regulate both pancreatic exocrine secretion and intracellular processes. These receptors are potential sites of action for therapeutic agents in the treatment of pancreatitis. Cholecystokinin (CCK) receptor antagonists, which may reduce the level of metabolic "stress" on acinar cells, have been shown to mitigate the severity of acute pancreatitis in a number of models. Not all studies have shown a benefit, however, and differences may exist between different structural classes of antagonists. Because increased pancreatic stimulation due to loss of feedback inhibition of CCK has been proposed to contribute to the pain of some patients with chronic pancreatitis, CCK receptor antagonists could also be of benefit in this setting. Somatostatin and its analogs diminish pancreatic secretion of water and electrolytes and have been effective in treating pancreatic fistulas and pseudocysts. These agents are also being evaluated for their ability to reduce pain in chronic pancreatitis (perhaps by reducing ductal pressure by diminishing secretory volume) and mitigating the severity of acute pancreatitis (possibly by reducing the metabolic load on acinar cells). Recently described secretin receptor antagonists may also have therapeutic value as a means of selectively inhibiting pancreatic secretion of water and electrolytes.

Entities:  

Mesh:

Substances:

Year:  1992        PMID: 1340060      PMCID: PMC2589733     

Source DB:  PubMed          Journal:  Yale J Biol Med        ISSN: 0044-0086


  22 in total

1.  Pancreatic ascites and effusion. Risk factors for failure of conservative therapy and the role of octreotide.

Authors:  D Parekh; I Segal
Journal:  Arch Surg       Date:  1992-06

2.  Effects of the cholecystokinin receptor antagonist L-364,718 on experimental pancreatitis in mice.

Authors:  M Silverman; C Ilardi; S Bank; V Kranz; S Lendvai
Journal:  Gastroenterology       Date:  1989-01       Impact factor: 22.682

3.  Pancreatic exocrine secretion in acute experimental pancreatitis.

Authors:  C Niederau; M Niederau; R Lüthen; G Strohmeyer; L D Ferrell; J H Grendell
Journal:  Gastroenterology       Date:  1990-10       Impact factor: 22.682

4.  Treatment of pancreatic pseudocysts with octreotide.

Authors:  L Gullo; L Barbara
Journal:  Lancet       Date:  1991-08-31       Impact factor: 79.321

Review 5.  Diagnosis of chronic pancreatitis.

Authors:  C Niederau; J H Grendell
Journal:  Gastroenterology       Date:  1985-06       Impact factor: 22.682

6.  Amelioration of cholinergic-induced pancreatitis with a selective cholecystokinin receptor antagonist.

Authors:  A J Bilchik; K A Zucker; T E Adrian; I M Modlin
Journal:  Arch Surg       Date:  1990-12

7.  Effect of a new cholecystokinin receptor antagonist CR 1392 on caerulein-induced acute pancreatitis in rats.

Authors:  M Otsuki; S Tani; Y Okabayshi; T Nakamura; M Fujii; T Fujisawa; S Baba; H Itoh
Journal:  Pancreas       Date:  1989       Impact factor: 3.327

8.  Protective action of luminal bile salts in necrotizing acute pancreatitis in mice.

Authors:  G Gomez; C M Townsend; D W Green; S Rajaraman; T Uchida; G H Greeley; R D Soloway; J C Thompson
Journal:  J Clin Invest       Date:  1990-07       Impact factor: 14.808

9.  Functional recovery of the exocrine pancreas after acute pancreatitis.

Authors:  C J Mitchell; M J Playforth; J Kelleher; M J McMahon
Journal:  Scand J Gastroenterol       Date:  1983-01       Impact factor: 2.423

10.  Fasting prevents acute pancreatitis induced by cerulein in rats.

Authors:  M Otsuki; S Tani; Y Okabayashi; M Fujii; T Nakamura; T Fujisawa; M Koide; H Itoh
Journal:  Dig Dis Sci       Date:  1990-07       Impact factor: 3.199

View more
  1 in total

1.  Cerulein-induced acute pancreatitis in PACAP knockout mice.

Authors:  Yusuke Sakurai; Norihito Shintani; Akihiro Arimori; Ken-Ichi Hamagami; Naoko Higuchi; Hiroaki Inoue; Kazuya Ikeda; Atsuko Hayata; Hitoshi Hashimoto; Akemichi Baba
Journal:  J Mol Neurosci       Date:  2010-06-22       Impact factor: 3.444

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.