A common pathway of nitric oxide release from AZD3582 and glyceryl trinitrate

التفاصيل البيبلوغرافية
العنوان: A common pathway of nitric oxide release from AZD3582 and glyceryl trinitrate
المؤلفون: Nina Grosser, Janet Hoogstraate, Henning Schröder, Georg Berndt
المصدر: European Journal of Pharmaceutical Sciences. 21:331-335
بيانات النشر: Elsevier BV, 2004.
سنة النشر: 2004
مصطلحات موضوعية: Molsidomine, Swine, Pharmaceutical Science, Stimulation, Naphthalenes, Pharmacology, Nitric Oxide, Nitric oxide, Nitroglycerin, chemistry.chemical_compound, Naproxen, medicine, Animals, Cyclooxygenase Inhibitors, Nitric Oxide Donors, Cyclic GMP, Kidney, biology, Linsidomine, medicine.anatomical_structure, Mechanism of action, chemistry, Biochemistry, cardiovascular system, biology.protein, LLC-PK1 Cells, Liberation, Cyclooxygenase, medicine.symptom, circulatory and respiratory physiology, medicine.drug
الوصف: 4-(Nitrooxy)-butyl-(S)-2-(6-methoxy-2-naphthyl)-propanoate (AZD3582) is a cyclooxygenase (COX)-inhibiting nitric oxide donator (CINOD). It donates nitric oxide (NO) in biological systems through as yet unidentified mechanisms. cGMP, a marker of intracellularly generated NO, was increased up to 27-fold over basal levels by AZD3582 (1-30microM) in LLC-PK1 kidney epithelial cells. A 5h pretreatment with glyceryl tinitrate (GTN, 0.1-1microM) attenuated the cGMP response to a subsequent challenge with AZD3582 or GTN. Similarly, AZD3582 (10-30microM) pretreatment reduced the increase in cGMP on subsequent incubation with AZD3582 or GTN. In contrast, cGMP stimulation by SIN-1, which releases NO independently of enzymatic catalysis, remained unimpaired in cells pretreated with GTN or AZD3582. Our results demonstrate that AZD3582 decreases the sensitivity of the guanylyl cyclase/cGMP system to GTN and vice versa. This suggests that bioactivation pathways for organic nitrates, which involve enzymatic catalysis, may be responsible for NO donation from AZD3582.
تدمد: 0928-0987
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0cfdf811765a14f858c7e1430ddab61
https://doi.org/10.1016/j.ejps.2003.10.020
حقوق: OPEN
رقم الأكسشن: edsair.doi.dedup.....e0cfdf811765a14f858c7e1430ddab61
قاعدة البيانات: OpenAIRE