Synthesis of an analog of human calcitonin gene related peptide, [Asu]-h-CGRP

The analog of h-CGRP, des-Ala-deamino-dicarba-h-CGRP, was synthesized by the combination of the conventional solution and the solid phase peptide synthesis methods. This analog showed stronger and longer-lasting hypocalcemic and hypophosphatemic activities than the natural hormone.     

Synthesis of an analog of human calcitonin gene related peptide, [Asu2,7]-h-CGRP

Summary The analog of h-CGRP, des-Ala-deamino-dicarba-h-CGRP, was synthesized by the combination of the conventional solution and the solid phase peptide synthesis methods. This analog showed stronger and longer-lasting hypocalcemic and hypophosphatemic activities than the natural hormone.30 September 1986     

Spectroscopic study of the disulfide bond in oxidized glutathione

Summary Raman and circular dichroism spectra are used for obtaining structural information on the disulfide bridge in oxidized glutathione. Quantitative estimates of dihedral angles and bond angles are proposed.     

Early stimulation of protein kinase activity during hormonal meiosis reinitiation in starfish ovocytes]

Total endogenous protein kinase activity has been compared in homogenates prepared from Marthasterias glacialis and Asterias rubens oocytes treated or not by 1-methyladenine, the hormone which triggers meiosis reinitiation. A 5 mn treatment at the threshold 10(-7) M concentration causes a significant increase (+ 20%) of these activities. This stimulation is maintained or even enhanced when homogenates are complemented with exogenous histones.     

Radioimmunoassay of hormonal activity of Gobius niger L. testicular interstitial tissue in organ culture: spontaneous activity and stimulation by pituitary gland]

After the interstitial tissue was cultivated, the radio-immunoassay revealed in the media very small quantities of free testosterone but much larger quantities of testosterone conjugates as glucuronids and sulfates. Association of pituitaries increases greatly the secretion. 12-13 days precultivated pituitaires retain close to 70% of their stimulating potency.     

Assembly of MHC class I peptide complexes from the perspective of disulfide bond formation

Assembly of functional major histocompatibility complex (MHC) class I peptide complexes within the endoplasmic reticulum is critically important for the development of an adaptive immune response. The highly regulated loading of peptides onto MHC class I molecules is controlled by a multi-component chaperone system called the MHC class I peptide loading complex. The recent identification of the thioredoxin family member ERp57 as a component of the loading complex led to an interesting question: Why is there a thiol-disulfide oxidoreductase inside a complex dedicated to inserting peptides into a receptor binding site? Most recently, specific ERp57-mediated disulfide bond rearrangements have been identified inside the loading complex. What these biochemical events mean for the peptide loading process remains a matter of conjecture. While several important questions wait to be answered, this review intends to summarize our current view of the oxidative folding of MHC class I molecules and addresses the question of how the receptor ligand interaction might be regulated by thiol-based redox reactions.     

Synthesis and some characteristics of [13C]-specially enriched tetragastrin and the related compound

[13C]-enriched tetragastrin and the related compound were synthesized in solution. Conversion of S-[13C]methylated tetragastrin to the enriched tetragastrin gave 10.5 ppm upfield chemical shift of Cepsilon resonance. The potency of the synthetic tetragastrin to stimulate gastric acid secretion was virtually identical with that of pentagastrin (ICI).     

Synthesis and some characteristics of [13C]-specially enriched tetragastrin and the related compound

Summary [¹³C]-enriched tetragastrin and the related compound were synthesized in solution. Conversion of S-[¹³C]-methylated tetragastrin to the enriched tetragastrin gave 10.5 ppm upfield chemical shift of C resonance. The potency of the synthetic tetragastrin to stimulate gastric acid secretion was virtually identical with that of pentagastrin (ICI).Acknowledgment. A part of this research was supported by scientific research funds (No. 944059, 048253) from the Japanese Ministry of Education.     

Synthesis and pharmacological properties of [1-N4-dimethyl-asparagine]-angiotensin II

Summary [1-N⁴-Dimethyl-asparagine]-angiotensin II was synthesized by Merrifield's solid-phase procedure. The analogue gave rat blood pressure about 70% relative potency to Hypertensin (Ciba). Rabbit aorta strips gave intrinsic activity _E=1, a PD₂ of 6.92±0.09 and an affinity relative to [Asn¹]-angiotensin II of 6.5%.The editors do not hold themselves responsible for the opinions expressed in the authors' brief reports. — Les auteurs sont seuls responsables des opinions exprimées dans ces brèves communications. — Für die Kurzmitteilungen ist ausschliesslich der Autor verantwortlich. — Per le brevi comunicazioni è responsabile solo l'autore. — . — Solo los autores son responsables de las opiniones expresadas en estas comunicationes breves.Acknowledgment. The authors wish to express their appreciation to Dr Emanuel Escher, School of Medicine, Centre Hospitalier Universitaire, Sherbrooke, Quebec, for his help in providing the biological data and critical comments.     

[4-proline, 8-isoleucine]-oxytocin and [4-leucine, 8-isoleucine]-oxytocin,possible intermediates in the evolutionary series of neurohypophysial hormones: Synthesis and some pharmacological properties

Zusammenfassung [4-Prolin, 8-Isoleucin]-Oxytocin und [4-Leucin, 8-Isoleucin]-Oxytocin wurden als mögliche Glieder in der entwicklungsgeschichtlichen Reihe der Neurohypophysenhormone synthetisiert und pharmakologisch geprüft.     

Influence of age on the plasma hormonal iodine response to thyrotropin injection in young calves]

The influence of age upon the increase in plasma hormonal iodine level following an intravenous injection of bovine TSH (0.2 USP units/kg) was studied in young jersey calves. The response to TSH increased between birth and the 7th day, then decreased regularly until the end of the third month. Reasons for these variations are discussed according to some results obtained following TSH injections.     

Synthesis and pharmacological properties of [1-N4-dimethyl-asparagine]-angiotensin II.

[1-N4-Dimethyl-asparagine]-angiotensin II was synthesized by Merrifield's solid-phase procedure. The analogue gave rat blood pressure about 70% relative potency to Hypertension (Ciba). Rabbit aorta strips gave intrinsic activity alpha E = 1, a PD2 of 6.92 +/- 0.09 and an affinity relative to [Asn1]-angiotensin II of 6.5%.     

Synthesis of [4-leucine]-arginine-vasotocin,a natriuretic analogue of arginine-vasotocin

Zusammenfassung Es wird die Synthese des 4-Leucin-Analogen des Arginin-vasotocins (=[Leu⁴, Arg⁸]-oxytocin) beschrieben.     

Response to an antiestrogen as a criterion for hormonal sensitivity of endometrial cancer]

A test is described for the evaluation of hormone sensitivity of endometrial cancer in vivo. The concentrations of progesterone and estradiol receptors, and the activities of ornithine-decarboxylase and 17 beta-hydroxysteroid oxido-reductase enzymes have been measured in the tumor, before and after administration of the anti-estrogen tamoxifen. The responses observed, in particular the increase of progesterone receptor, could allow a more rational approach to hormonal therapy of endometrial cancer.     

Synthesis and biological activity of peptides related to bradykinin

Zusammenfassung Die Synthese von 6 Polypeptiden aus den im Bradykinin vorkommenden Aminosäuren wird beschrieben. Das Nonapeptid H-l-Arg-l-Pro-l-Pro-Gly-l-Phe-l-Ser-l-Pro-l-Phe-l-Arg-OH zeigte hohe Bradykinin-ähnliche Wirksamkeit in verschiedenen biologischen Testen.     

Synthesis of [1-Aib]-angiotensin II, an analogue with higher potency than [1-Asn,5-Val]-angiotensin II

[1-Aib]-angiotensin II was synthesized by Merrifield's solid-phase procedure. The analogue, tested on rabbit aorta strips, showed intrinsic activity alpha E = 1, and when tested on rat blood pressure it gave a pD2 of 8.06; a 3.2 +/- 1.3-fold higher potency than the Ciba-Hypertensin standard.