The role of the glia limitans in ADP-induced pial arteriolar relaxation in intact and ovariectomized female rats

We examined whether the glia limitans (GL) influences pial arteriolar relaxation elicited in vivo by the purinergic (P2Y1 receptor) agonist ADP in female rats, and whether that influence is altered in ovariectomized (Ovx) females. A validated model for GL injury was used, topical application of the...

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Bibliographic Details
Published in:American journal of physiology. Heart and circulatory physiology 2005, Vol.57 (1), p.H382-H388
Main Authors: XU, Hao-Liang, SHUHUA YE, BAUGHMAN, Verna L, FEINSTEIN, Douglas L, PELLIGRINO, Dale A
Format: Article
Language:English
Subjects:
Biological and medical sciences
Fundamental and applied biological sciences. Psychology
Hysterectomy
Nitric oxide
Pulmonary arteries
Vertebrates: cardiovascular system
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Summary:We examined whether the glia limitans (GL) influences pial arteriolar relaxation elicited in vivo by the purinergic (P2Y1 receptor) agonist ADP in female rats, and whether that influence is altered in ovariectomized (Ovx) females. A validated model for GL injury was used, topical application of the gliotoxin L-{alpha}-aminoadipic acid (L-{alpha}AAA), 24 h before the study. In both intact and Ovx females, L-{alpha}AAA had no effect on responses to the NO donor, S-nitroso-N-acetyl penicillamine, but ADP-induced pial arteriolar dilations were significantly reduced (by 33-90%), compared with vehicle-treated controls. When NG-nitro-L-arginine (L-NNA) was administered to L-{alpha}AAA-treated rats, the ADP response was virtually lost in intact females, but no further reductions were observed in the Ovx rats. On the other hand, in L-{alpha}AAA-treated Ovx females, when the gap junction blocker, Gap 27, was subsequently added to the suffusate, ADP reactivity fell to very low levels. In vehicle-treated control rats, L-NNA and Gap 27 reduced ADP reactivity by ~50% in intact and Ovx females, respectively. An earlier study indicated that the endothelium was a key site of influence for L-NNA (intact) and Gap 27 (Ovx). Thus present and previous results imply that the ADP response in pial arterioles represents the additive actions of an endothelial and a GL component. That supposition was confirmed in the present study by the finding that combining endothelial and GL injury produced an essentially complete loss of ADP reactivity in both intact and Ovx females. Finally, topical application of the selective P2Y1 antagonist, MRS-2179, was associated with a nearly complete suppression of the ADP response in both intact and Ovx females. These results suggest that 1) ADP-induced pial arteriolar dilation involves additive contributions from P2Y1 receptors present in both vascular endothelium and the GL; 2) the influence of the GL component is not altered by ovariectomy; and 3) the gap junction-dependent component of the ADP response in Ovx females is unlikely to include the GL and probably resides in the vessels themselves. [PUBLICATION ABSTRACT]
ISSN:0363-6135
1522-1539