Da. Walsh et al., AT(1) RECEPTOR CHARACTERISTICS OF ANGIOTENSIN ANALOG BINDING IN HUMANSYNOVIUM, British Journal of Pharmacology, 112(2), 1994, pp. 435-442
1 Angiotensin II (AII) reduces blood flow, modulates vascular remodell
ing and is a growth factor. Human inflammatory arthritides are charact
erized by synovial hypoperfusion, hypoxia and proliferation. We aimed
to localize and characterize receptors for AII in human synovium. 2 We
used quantitative in vitro receptor autoradiography with [I-125]-(Sar
(1), Ile(8))AII and [I-125]-AII on human synovium from patients with c
hondromalacia patellae, osteoarthritis and rheumatoid arthritis. 3 [I-
125]-(Sar(1), Ile(8))AII and [I-125]-AII bound to similar sites on syn
ovial blood vessels, lining cells and stroma. Binding to microvessels
(<100 mu m diameter) was more dense than to arteriolar media, and vasc
ular binding was more dense than that to lining cells and stroma. 4 Mi
crovessels and arterioles which displayed angiotensin converting enzym
e-like immunoreactivity also displayed specific binding of [I-125]-(Sa
r(1), Ile(8))AII. 5 Specific binding of [I-125]-(Sar(1), Ile(8))AII to
each structure was completely inhibited by 10 mu M dithiothreitol and
was inhibited by unlabelled ligands with the rank order of potency (S
ar(1), Ile(8))AII > AII > losartan = SKF108566 much greater than PD123
319 indicating an AT(1) subclass of angiotensin receptor. 6 GTP gamma
S (1 mu M) abolished specific binding of [I-125]-AII and abolished the
high affinity component of the binding inhibition curve for AII again
st [I-125]-(Sar(1), Ile(8))AII, indicating G protein coupling. 7 The d
istribution of [I-125]-(Sar(1), Ile(8))AII binding sites was similar i
n all disease groups and no significant differences in binding densiti
es, affinities or specificities were observed between disease groups.
8 Locally generated AII may act on synovial AT(1) receptors to modulat
e synovial perfusion and growth. Specific AT(1) receptor antagonists s
hould help elucidate the role of angiotensins in human arthritis.