Cai R Z, Karashima T, Guoth J, Szoke B, Olsen D, Schally A V
Proc Natl Acad Sci U S A. 1987 Apr;84(8):2502-6. doi: 10.1073/pnas.84.8.2502.
We synthesized a series of octapeptide analogs of somatostatin, containing N-terminal tryptophan or another amino acid followed by the hexapeptide sequences Cys-Phe-D-Trp-Lys-Thr-Cys or Cys-Tyr-D-Trp-Lys-Val-Cys and a C-terminal threoninamide or tryptophanamide. After purification by HPLC, the inhibitory activities of these analogs on the release of growth hormone (somatotropin) in rats were determined in vivo. The eight octapeptides with an N-terminal tryptophan residue were found to have a greater inhibitory effect than somatostatin. The most potent of these analogs, D-Trp-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr-NH2, was 94.3 times more active than somatostatin. The other analogs, in order of decreasing potency, were Ac-Trp-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr-NH2, D-Trp(For)-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr-NH2, D-Trp-Cys-Tyr-D-Trp-Lys-Val-Cys-Thr-NH2, Ac-Trp(For)-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr-NH2, Ac-Trp-Cys-Tyr-D-Trp-Lys-Val-Cys-Thr-NH2, D-Trp-Cys-Phe-D-Trp-Lys-Thr-Cys-Trp-NH2, and D-Trp-Cys-Tyr-D-Trp-Lys-Val-Cys-Trp-NH2. The growth hormone inhibitory activity of these analogs was from 53.7 to 11.6 times greater than that of somatostatin. The octapeptides containing D- or L-tryptophan at the N-terminus, phenylalanine at position 3, and threonine at position 6 exhibited a greater inhibitory effect on growth hormone release than that of the analogs with tyrosine and valine at positions 3 and 6, respectively. Substitution of D-tryptophan for D-phenylalanine at the N-terminus in the octapeptide containing phenylalanine in the third, threonine in the sixth, and threoninamide in the C-terminal position also increased the growth hormone-release inhibitory activity. Time-course assay showed that D-Trp-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr-NH2 (RC-98-I), in a dose of 1 microgram/kg of body weight, inhibited the release of growth hormone for at least 3 hr. In view of their high activity and prolonged duration of action, some of these analogs could be useful clinically.
我们合成了一系列生长抑素的八肽类似物,它们含有N端色氨酸或其他氨基酸,随后是六肽序列Cys-Phe-D-Trp-Lys-Thr-Cys或Cys-Tyr-D-Trp-Lys-Val-Cys,以及C端苏氨酰胺或色氨酰胺。通过高效液相色谱法纯化后,在体内测定了这些类似物对大鼠生长激素(促生长素)释放的抑制活性。发现八个带有N端色氨酸残基的八肽比生长抑素具有更强的抑制作用。其中最有效的类似物D-Trp-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr-NH2的活性比生长抑素高94.3倍。其他类似物,按效力递减顺序依次为:Ac-Trp-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr-NH2、D-Trp(For)-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr-NH2、D-Trp-Cys-Tyr-D-Trp-Lys-Val-Cys-Thr-NH2、Ac-Trp(For)-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr-NH2、Ac-Trp-Cys-Tyr-D-Trp-Lys-Val-Cys-Thr-NH2、D-Trp-Cys-Phe-D-Trp-Lys-Thr-Cys-Trp-NH2和D-Trp-Cys-Tyr-D-Trp-Lys-Val-Cys-Trp-NH2。这些类似物的生长激素抑制活性比生长抑素高53.7至11.6倍。在N端含有D-或L-色氨酸、第3位为苯丙氨酸且第6位为苏氨酸的八肽对生长激素释放的抑制作用比在第3位和第6位分别为酪氨酸和缬氨酸的类似物更强。在第3位含有苯丙氨酸、第6位含有苏氨酸且C端为苏氨酰胺的八肽中,将N端的D-苯丙氨酸替换为D-色氨酸也增加了生长激素释放抑制活性。时间进程分析表明,剂量为1微克/千克体重的D-Trp-Cys-Phe-D-Trp-Lys-Thr-Cys-Thr-NH2(RC-98-I)可抑制生长激素释放至少3小时。鉴于它们的高活性和延长的作用持续时间,其中一些类似物可能在临床上有用。