The present study provides evidence that retinal tissue may profoundly
influence the retinal arterial smooth muscle cell tone by releasing a
n unknown retinal relaxing factor. Isolated bovine retinal arteries wi
th and without adhering retinal tissue were mounted in a wire myograph
for isometric tension recordings. The maximal contraction induced by
prostaglandin F-2 alpha was 0.95+/-0.7 mN (n=6) in the presence and 5.
15+/-0.76 mN (n=6) in the absence of adhering retinal tissue. The cont
ractions induced by U-46619, serotonin, and endothelin-l were similarl
y blocked in the presence of retinal tissue. The K+ 120 mmol/L-induced
contraction was not significantly affected (2.8+/-0.7 mN, n=6, in the
presence and 3.6+/-0.7 mN, n=6, in the absence of retinal tissue). Pl
acing a piece of bovine retinal tissue in the proximity of a contracte
d (ie, with prostaglandin F-2 alpha) retinal artery induced a complete
relaxation of the retinal vessel, suggesting the involvement of a dif
fusible chemical vasorelaxant. Also porcine, canine, and ovine retinal
tissue completely relaxed the contracted (with prostaglandin F-2 alph
a) bovine retinal artery. Other smooth muscle preparations, including
rat mesenteric and renal arteries and rat main bronchi, also relaxed w
ith the application of a piece of bovine retinal tissue. Incubation of
bovine retinas in a Krebs-Ringer bicarbonate solution yielded a solut
ion that relaxed isolated precontracted bovine retinal arteries, confi
rming the involvement of a diffusible chemical messenger. Hexane extra
ction, heating the solution to 70 degrees C, or treatment with trypsin
did not alter the relaxing properties of the incubation solution. The
characteristics of the retinal relaxing factor do not correspond with
those of nitric oxide, prostanoids, adenosine, acetylcholine, or any
other of the known vasoactive neurotransmitters released from the reti
na. Our results suggest that retinal arterial tone is controlled by a
diffusible, hydrophilic, and heat-stable relaxing factor that does not
correspond with a known vasoactive molecule formed within the retina.