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Tytuł pozycji:

The kinin system: suggestions to broaden some prevailing concepts.

Tytuł:
The kinin system: suggestions to broaden some prevailing concepts.
Autorzy:
Erdös EG; Department of Pharmacology, College of Medicine, University of Illinois at Chicago, Chicago, IL 60612-7344, USA. />Deddish PA
Źródło:
International immunopharmacology [Int Immunopharmacol] 2002 Dec; Vol. 2 (13-14), pp. 1741-6.
Typ publikacji:
Journal Article; Research Support, U.S. Gov't, P.H.S.; Review
Język:
English
Imprint Name(s):
Original Publication: Amsterdam ; New York : Elsevier Science, c2001-
MeSH Terms:
Angiotensin-Converting Enzyme Inhibitors/*pharmacology
Kallikrein-Kinin System/*physiology
Bradykinin/pharmacology ; Humans ; Kallikreins/metabolism ; Kidney/drug effects ; Kidney/enzymology ; Kidney/metabolism ; Kinins/metabolism ; Receptors, Bradykinin/metabolism
Liczba referencji:
30
Grant Information:
HL36473 United States HL NHLBI NIH HHS; HL58118 United States HL NHLBI NIH HHS
Substance Nomenclature:
0 (Angiotensin-Converting Enzyme Inhibitors)
0 (Kinins)
0 (Receptors, Bradykinin)
EC 3.4.21.- (Kallikreins)
S8TIM42R2W (Bradykinin)
Entry Date(s):
Date Created: 20021220 Date Completed: 20030808 Latest Revision: 20191106
Update Code:
20240104
DOI:
10.1016/s1567-5769(02)00166-2
PMID:
12489787
Czasopismo naukowe
The existence and importance of the kallikrein-kinin-kininase system, especially in the circulation, has taken over three-quarters of a century to be established. Finding the multiple components derived from renin-angiotensin and their functions stretched over a century [Erdös EG. Perspectives on the early history of angiotensin-converting enzyme-recent follow-ups. In: Giles TD, editor. Angiotensin-converting enzyme (ACE): clinical and experimental insights. Fort Lee: Health Care Communications; 2001, p. 3-16]. Although the discoveries were made independently, it was shown in 1970 that the angiotensin I-converting enzyme (ACE) is identical with kininase II, previously discovered by us, thus, a single protein can regulate either the activation or inactivation of the two peptide products. It followed that inhibitors of ACE can affect both processes [Bhoola KD, Figueroa CD, Worthy K. Bioregulation of kinins: kallikreins, kininogens, and kininases. Pharmacol Rev 1992;44:1-80]. After being engaged for a long time in characterizing the metabolism of various bio-active peptides, we, as well as others, noticed that the effect of ACE inhibitors go beyond simply blocking angiotensin (Ang) II release and bradykinin (BK) inactivation by the enzyme (Kaplan AP, Joseph K, Silverberg M. Pathways for bradykinin formation and inflammatory disease. J Allergy Clin Immunol 2002; 109(2):195-209, Yamada K, Erd6s EG. Kallikrein and prekallikrein of the isolated basolateral membrane of rat kidney. Kidney Int 1982;22:331-7]. It also became apparent to us that in the complex multistep reactions needed to activate the kallikrein-kinin system, there should be some shortcuts-shunts-to accelerate and simplify important processes. Thus, some basic tenets developed after decades of intensive laboratory investigations-and by now generally accepted-can be challenged. For example, it should be considered that the activities of BK and Lys BK (kallidin) can be substantially different, and that sequentially linked reactions, starting with prokallikrein activation and leading to kinin release from kininogen and inhibition of kininases, may be only one way to activate kinin receptors. A summary of some suggested alterations on prevailing concepts is given below.

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