Abstract
Alpha-1 adrenergic receptors were examined in rat caudal artery using radioligand binding of [125I]labeled BE 2254 (125IBE) and in vivo contraction measurements. 125IBE bound rapidly and reversibly to a single class of high affinity binding sites in membrane preparations of caudal artery. Scatchard analysis gave an equilibrium dissociation constant (K(D)) of 110 pM and a density of binding sites of 115 fmol/mg of protein. Antagonists inhibited 125IBE binding and phenylephrine-induced contractions competitively, with an order of potency of prazosin > ARC 239 > phentolamine > yohimbine. pA2 values for inhibition of phenylephrine-induced contraction correlated well with K(D) values for inhibition of specific 125IBE binding. A number of other full and partial agonists also caused contraction of caudal arteries with an order of potency of epinephrine > norepinephrine > phenylephrine > methoxamine. The order of potency of agonists and the potencies of antagonists suggests that the contractile responses of rat caudal artery were mediated by alpha-1 adrenergic receptors. The EC50 values of partial agonists in causing contraction correlated well with their K(D) values for inhibition of specific 125IBE binding. However, the EC50 values for full agonists were 30 to 200 times lower than their K(D) values. Treatment of caudal arteries in vitro with 0.1 μM phenoxybenzamine for 10 min to inactivate alpha adrenergic receptors decreased both the potency of full agonists in causing contraction and the maximal contractile response. Functional equilibrium dissociation constants calculated from contraction experiments using phenoxybenzamine agreed well with K(D)'s determined from binding studies; however, phenoxybenzamine reduced 125IBE binding sites by 50%, whereas the theoretical reduction in functional alpha adrenergic receptors averaged 96%. These data suggest that 125IBE labels the alpha-1 adrenergic receptors mediating contraction of rat caudal artery. When receptor density is reduced, the potencies of agonists in activating the receptors agree well with their potencies in binding to the receptors, suggesting that there is a pool of 'spare' alpha-1 adrenergic receptors in this tissue.
| Original language | English |
|---|---|
| Pages (from-to) | 678-686 |
| Number of pages | 9 |
| Journal | Journal of Pharmacology and Experimental Therapeutics |
| Volume | 239 |
| Issue number | 3 |
| State | Published - 1986 |
| Externally published | Yes |
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All Science Journal Classification (ASJC) codes
- Pharmacology
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Alpha-1 adrenergic receptor binding and contraction of rat caudal artery. / Abel, Peter W.; Minneman, K. P.
In: Journal of Pharmacology and Experimental Therapeutics, Vol. 239, No. 3, 1986, p. 678-686.Research output: Contribution to journal › Article
}
TY - JOUR
T1 - Alpha-1 adrenergic receptor binding and contraction of rat caudal artery
AU - Abel, Peter W.
AU - Minneman, K. P.
PY - 1986
Y1 - 1986
N2 - Alpha-1 adrenergic receptors were examined in rat caudal artery using radioligand binding of [125I]labeled BE 2254 (125IBE) and in vivo contraction measurements. 125IBE bound rapidly and reversibly to a single class of high affinity binding sites in membrane preparations of caudal artery. Scatchard analysis gave an equilibrium dissociation constant (K(D)) of 110 pM and a density of binding sites of 115 fmol/mg of protein. Antagonists inhibited 125IBE binding and phenylephrine-induced contractions competitively, with an order of potency of prazosin > ARC 239 > phentolamine > yohimbine. pA2 values for inhibition of phenylephrine-induced contraction correlated well with K(D) values for inhibition of specific 125IBE binding. A number of other full and partial agonists also caused contraction of caudal arteries with an order of potency of epinephrine > norepinephrine > phenylephrine > methoxamine. The order of potency of agonists and the potencies of antagonists suggests that the contractile responses of rat caudal artery were mediated by alpha-1 adrenergic receptors. The EC50 values of partial agonists in causing contraction correlated well with their K(D) values for inhibition of specific 125IBE binding. However, the EC50 values for full agonists were 30 to 200 times lower than their K(D) values. Treatment of caudal arteries in vitro with 0.1 μM phenoxybenzamine for 10 min to inactivate alpha adrenergic receptors decreased both the potency of full agonists in causing contraction and the maximal contractile response. Functional equilibrium dissociation constants calculated from contraction experiments using phenoxybenzamine agreed well with K(D)'s determined from binding studies; however, phenoxybenzamine reduced 125IBE binding sites by 50%, whereas the theoretical reduction in functional alpha adrenergic receptors averaged 96%. These data suggest that 125IBE labels the alpha-1 adrenergic receptors mediating contraction of rat caudal artery. When receptor density is reduced, the potencies of agonists in activating the receptors agree well with their potencies in binding to the receptors, suggesting that there is a pool of 'spare' alpha-1 adrenergic receptors in this tissue.
AB - Alpha-1 adrenergic receptors were examined in rat caudal artery using radioligand binding of [125I]labeled BE 2254 (125IBE) and in vivo contraction measurements. 125IBE bound rapidly and reversibly to a single class of high affinity binding sites in membrane preparations of caudal artery. Scatchard analysis gave an equilibrium dissociation constant (K(D)) of 110 pM and a density of binding sites of 115 fmol/mg of protein. Antagonists inhibited 125IBE binding and phenylephrine-induced contractions competitively, with an order of potency of prazosin > ARC 239 > phentolamine > yohimbine. pA2 values for inhibition of phenylephrine-induced contraction correlated well with K(D) values for inhibition of specific 125IBE binding. A number of other full and partial agonists also caused contraction of caudal arteries with an order of potency of epinephrine > norepinephrine > phenylephrine > methoxamine. The order of potency of agonists and the potencies of antagonists suggests that the contractile responses of rat caudal artery were mediated by alpha-1 adrenergic receptors. The EC50 values of partial agonists in causing contraction correlated well with their K(D) values for inhibition of specific 125IBE binding. However, the EC50 values for full agonists were 30 to 200 times lower than their K(D) values. Treatment of caudal arteries in vitro with 0.1 μM phenoxybenzamine for 10 min to inactivate alpha adrenergic receptors decreased both the potency of full agonists in causing contraction and the maximal contractile response. Functional equilibrium dissociation constants calculated from contraction experiments using phenoxybenzamine agreed well with K(D)'s determined from binding studies; however, phenoxybenzamine reduced 125IBE binding sites by 50%, whereas the theoretical reduction in functional alpha adrenergic receptors averaged 96%. These data suggest that 125IBE labels the alpha-1 adrenergic receptors mediating contraction of rat caudal artery. When receptor density is reduced, the potencies of agonists in activating the receptors agree well with their potencies in binding to the receptors, suggesting that there is a pool of 'spare' alpha-1 adrenergic receptors in this tissue.
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M3 - Article
C2 - 2879031
AN - SCOPUS:0022916924
VL - 239
SP - 678
EP - 686
JO - Journal of Pharmacology and Experimental Therapeutics
JF - Journal of Pharmacology and Experimental Therapeutics
SN - 0022-3565
IS - 3
ER -