[Synthesis and biological activity of an analogue of active fragment (SP-6) of substance P]

Yao Xue Xue Bao. 1994;29(7):553-7.
[Article in Chinese]

Abstract

SP-6 was synthesized by solid phase method in 95% purity on HPLC. The data obtained from amino acid analysis and fast atom bombardment were in good agreement with theoretical values. Intravenous injection of SP-6 in rabbits at the dosage of 14.3 micrograms/kg. resulted in blood pressure reduction of 4.4 kPa, i.e. 34% (P < 0.001). When the concentration of SP-6 in Tyrode solution was 5.2 x 10(-4) mg/ml the contraction of rabbit duodenum longitudinal muscle increased by 105%. (P < 0.001). When the concentration was more than 1 x 10(-3) mg/ml, the contractile effect was restrained significantly. Dropping 30 microliters of SP-6 (1 x 10(-3) mg/ml) to toad intestinum tenue mesenteriale in situ, the mesentery arterioles were expanded by 30%.

Publication types

  • English Abstract

MeSH terms

  • Animals
  • Blood Pressure / drug effects*
  • Bufo bufo
  • Duodenum / drug effects
  • Female
  • Male
  • Mesenteric Arteries / physiology
  • Muscle Contraction / drug effects*
  • Muscle, Smooth / drug effects
  • Oligopeptides / chemical synthesis
  • Oligopeptides / pharmacology*
  • Rabbits
  • Vasodilation / drug effects*

Substances

  • Oligopeptides
  • arginyl-threonyl-prolyl-prolyl-prolyl-seryl-glycine