Manning M, Cheng L L, Klis W A, Balaspiri L, Olma A, Sawyer W H, Wo N C, Chan W Y
Department of Biochemistry & Molecular Biology, Medical College of Ohio, Toledo 43699-0008, USA.
J Med Chem. 1995 May 12;38(10):1762-9. doi: 10.1021/jm00010a020.
We report the solid-phase synthesis of the D-Cys6 analogues of arginine-vasopressin (AVP), peptide 1, of the selective AVP vasopressor (V1a receptor) antagonist [1-(beta-mercapto-beta,beta-pentamethylenepropionic acid),2-O-methyltyrosine]arginine-vasopressin (d(CH2)5[Tyr(Me)2]-AVP, (A)), peptide 2, of the three nonselective antidiuretic/vasopressor (V2/V1a receptor) AVP antagonists d(CH2)5[Tyr(Et)2]VAVP (B), d(CH2)5[D-Tyr(Et)2]VAVP (C), and d(CH2)5[D-Phe2]VAVP (D) (where V = Val4), peptides 3-5, of the nonselective oxytocin (OT) antagonists d(CH2)5-[Tyr(Me)2]OVT (E) and d(CH2)5[Tyr(Me)2,Thr4,Tyr-NH2(9)]OVT (F) (where OVT = ornithine-vasotocin), peptides 6 and 7, and of the selective OT antagonists desGly-NH2,d(CH2)5[Tyr(Me)2,Thr4]OVT (G) and d(CH2)5]D-Trp2,Thr4]OVT (H), peptides 8 and 9. We also present the repeat syntheses of the previously reported d(CH2)5[D-Trp2]AVT (peptide 10) and its D-Cys6 analogue (peptide 11) (where AVT = arginine-vasotocin). Peptides 1-11 were assayed for agonistic and antagonistic activities in in vivo V1a, V2, and oxytocic assays and in in vitro oxytocic assays without and with 0.5 mM Mg2+. With V2 and V1a agonistic potencies of 0.82 and 0.41 units/mg, [D-Cys6]AVP has retained less than 0.3% of the V2 and V1a potencies of AVP. It exhibits no oxytocic activity and is an in vitro OT antagonist. pA2 = 6.67 (no Mg2+); pA2 = 5.24 (0.5 mM Mg2+). By contrast, with one or two exceptions, a D-Cys6/L-Cys6 interchange in antagonists 2-9, although resulting in reductions of antagonistic potencies in all assays for virtually all peptides 2-9 relative to A-H, has been well tolerated. For peptides 2-5, the anti-V2 and anti-V1a pA2 values range from approximately 5.54 to 7.33 and from 7.19 to 8.06, respectively; the range of in vitro anti-OT pA2 values (no Mg2+) is 7.35-7.87; with 0.5 mM Mg2+, the range is 7.24-8.21. Peptides 2 and 4 have in vivo anti-OT pA2s = 6.60 and 7.16, respectively. For peptides 6-9, the range of in vitro anti-OT pA2 values (no Mg2+) is 7.65-7.96; with 0.5 mM Mg2+, the range is 7.41-7.65, and the in vivo anti-OT pA2 values range from 6.85 to 7.33. With an in vivo anti-OT pA2 = 7.33, peptide 6 is equipotent with its parent E. The in vivo anti-OT potencies of peptides 7-9 are significantly reduced relative to those of F-H. The in vitro anti-OT (0.5 mM Mg2+) pA2 values of 10 and 11 are 7.54 and 7.50, both significantly lower than those previously reported.(ABSTRACT TRUNCATED AT 400 WORDS)
我们报道了精氨酸加压素(AVP)的D - Cys6类似物(肽1)、选择性AVP血管升压素(V1a受体)拮抗剂[1 -(β - 巯基 - β,β - 五亚甲基丙酸),2 - O - 甲基酪氨酸]精氨酸加压素(d(CH2)5[Tyr(Me)2]-AVP,(A))、肽2、三种非选择性抗利尿/血管升压素(V2/V1a受体)AVP拮抗剂d(CH2)5[Tyr(Et)2]VAVP(B)、d(CH2)5[D - Tyr(Et)2]VAVP(C)和d(CH2)5[D - Phe2]VAVP(D)(其中V = Val4)、肽3 - 5、非选择性催产素(OT)拮抗剂d(CH2)5 - [Tyr(Me)2]OVT(E)和d(CH2)5[Tyr(Me)2,Thr4,Tyr - NH2(9)]OVT(F)(其中OVT = 鸟氨酸血管加压素)、肽6和7以及选择性OT拮抗剂去甘氨酰胺,d(CH2)5[Tyr(Me)2,Thr4]OVT(G)和d(CH2)5]D - Trp2,Thr4]OVT(H)、肽8和9的固相合成。我们还展示了先前报道的d(CH2)5[D - Trp2]AVT(肽10)及其D - Cys6类似物(肽11)(其中AVT = 精氨酸血管加压素)的重复合成。对肽1 - 11进行了体内V1a、V2和催产素活性测定以及体外催产素活性测定(有无0.5 mM Mg2+)。[D - Cys6]AVP的V2和V1a激动活性分别为0.82和0.41单位/毫克,其V2和V1a活性保留不到AVP的0.3%。它无催产素活性,是一种体外OT拮抗剂。pA2 = 6.67(无Mg2+);pA2 = 5.24(0.5 mM Mg2+)。相比之下,但有一两个例外,拮抗剂2 - 9中D - Cys6/L - Cys6的互换,尽管相对于A - H几乎所有肽2 - 9在所有测定中拮抗活性降低,但仍具有良好耐受性。对于肽2 - 5,抗V2和抗V1a的pA2值分别约为5.54至7.33和7.19至8.06;体外抗OT的pA2值范围(无Mg2+)为7.35 - 7.87;有0.5 mM Mg2+时,范围为7.24 - 8.21。肽2和4的体内抗OT的pA2分别为6.60和7.16。对于肽6 - 9,体外抗OT的pA2值范围(无Mg2+)为7.65 - 7.96;有0.5 mM Mg2+时,范围为7.41 - 7.65,体内抗OT的pA2值范围为6.85至7.33。肽6的体内抗OT的pA2 = 7.33,与其母体E等效。肽7 - 9的体内抗OT活性相对于F - H显著降低。肽10和11的体外抗OT(0.5 mM Mg2+)pA2值分别为7.54和7.50,均显著低于先前报道的值。(摘要截短为400字)