Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 5 de 5
Filter
1.
Biomolecules & Therapeutics ; : 274-281, 2018.
Article in English | WPRIM | ID: wpr-714739

ABSTRACT

A previous study in humans demonstrated the sustained inhibitory effects of donepezil on acetylcholinesterase (AChE) activity; however, the effective concentration of donepezil in humans and animals is unclear. This study aimed to characterize the effective concentration of donepezil on AChE inhibition and impaired learning and memory in rodents. A pharmacokinetic study of donepezil showed a mean peak plasma concentration of donepezil after oral treatment (3 and 10 mg/kg) of approximately 1.2 ± 0.4 h and 1.4 ± 0.5 h, respectively; absolute bioavailability was calculated as 3.6%. Further, AChE activity was inhibited by increasing plasma concentrations of donepezil, and a maximum inhibition of 31.5 ± 5.7% was observed after donepezil treatment in hairless rats. Plasma AChE activity was negatively correlated with plasma donepezil concentration. The pharmacological effects of donepezil are dependent upon its concentration and AChE activity; therefore, we assessed the effects of donepezil on learning and memory using a Y-maze in mice. Donepezil treatment (3 mg/kg) significantly prevented the progression of scopolamine-induced memory impairment in mice. As the concentration of donepezil in the brain increased, the recovery of spontaneous alternations also improved; maximal improvement was observed at 46.5 ± 3.5 ng/g in the brain. In conclusion, our findings suggest that the AChE inhibitory activity and pharmacological effects of donepezil can be predicted by the concentration of donepezil. Further, 46.5 ± 3.5 ng/g donepezil is an efficacious target concentration in the brain for treating learning and memory impairment in rodents.


Subject(s)
Animals , Humans , Mice , Acetylcholinesterase , Biological Availability , Brain , Learning , Memory , Plasma , Rats, Hairless , Rodentia
2.
Journal of the Korean Pediatric Society ; : 562-567, 1998.
Article in Korean | WPRIM | ID: wpr-10406

ABSTRACT

Crohn' s disease is a chronic inflammatory disease that may affect any part of the gastrointestinal system and multiple extraintestinal organs. Right lower quadrant abdominal pain with fever may be mistaken as a acute appendicitis. Pancreatitis has rarely been reported as a complication of Crohn' s disease. However, we experienced one case of Crohn' s disease with pancreatitis : the histologic examination after appendectomy of a 12-year-old female child who complained about abdominal pain and high fever.


Subject(s)
Child , Female , Humans , Abdominal Pain , Appendectomy , Appendicitis , Crohn Disease , Fever , Pancreatitis
4.
Korean Journal of Hematology ; : 117-122, 1993.
Article in Korean | WPRIM | ID: wpr-720062

ABSTRACT

No abstract available.


Subject(s)
Lupus Coagulation Inhibitor
5.
Yonsei Medical Journal ; : 234-238, 1993.
Article in English | WPRIM | ID: wpr-183675

ABSTRACT

We measured plasma levels of fibrinogen degradation products (FgDP) with newly developed enzyme-linked immunosorbent assay based on monoclonal antibody to assess the fibrinogenolytic state in 52 patients with various liver diseases (27 patients with liver cirrhosis, 10 with chronic hepatitis, 7 with acute hepatitis, 6 with hepatocellular carcinoma, 2 with intrahepatic cholestasis). As compared with 20 healthy subjects (upper limit: 580 ng/ml), elevated plasma levels (660-32000 ng/ml) of FgDP were found in 19 (36.5%) patients. When analyzed according to the underlying disease categories, the magnitude of elevations of FgDP were most prominent in patients with chronic hepatitis. No correlation was found between plasma FgDP levels and serum AST or ALT activity. These findings indicate that increased primary fibrinogenolysis is not rare in liver disease, but poorly correlates with liver function.


Subject(s)
Humans , Chronic Disease , Enzyme-Linked Immunosorbent Assay , Fibrin Fibrinogen Degradation Products/metabolism , Fibrinolysis , Hepatitis/blood , Liver Diseases/blood
SELECTION OF CITATIONS
SEARCH DETAIL