Formation of 5α-reduced androgens in the testes and urogenital tract of the grey short-tailed opossum, Monodelphis domestica

2009 ◽  
Vol 21 (5) ◽  
pp. 649 ◽  
Author(s):  
Jean D. Wilson ◽  
Marilyn B. Renfree ◽  
Richard J. Auchus ◽  
Andrew J. Pask ◽  
Geoffrey Shaw

Testicular 5α-reduced androgens, largely 5α-androstane-3α,17β-diol (androstanediol), are responsible for virilisation of pouch young in one marsupial (the tammar wallaby), but are not formed until later in development in another marsupial (the brushtail possum) and in rodents. Because the mechanism of virilisation of the urogenital tract in the grey short-tailed opossum Monodelphis domestica has never been defined, androgen formation and metabolism were investigated in this species. Testis fragments from grey short-tailed opossums of a wide range of ages were incubated with [3H]-progesterone and the metabolites were separated by high-performance liquid chromatography (HPLC). The only 19-carbon metabolites identified in the youngest ages (5–26 days) and the major metabolites in adult testes were testosterone and androstenedione. At 30, 42 and 49 days of age, dihydrotestosterone and small amounts of androstanediol were present. Time-sequence studies indicated that dihydrotestosterone and androstanediol were formed from the 5α-reduction (and 3-keto reduction) of testosterone. In a second series of experiments, tissue fragments of a variety of urogenital tract tissues were incubated with [3H]-testosterone and the metabolites separated by HPLC. During the interval in which male urogenital tract differentiation takes place in this species (between Days 15 and 28), the major metabolite identified was dihydrotestosterone. We conclude that the timing of 5α-reductase expression in the testes of the grey short-tailed possum resembles that of rodents and the brushtail possum rather than that of the tammar wallaby and that dihydrotestosterone is probably the intracellular androgen responsible for virilisation of the urogenital tract in this species.


2005 ◽  
Vol 17 (6) ◽  
pp. 603 ◽  
Author(s):  
Jean D. Wilson ◽  
Geoffrey Shaw ◽  
Marilyn B. Renfree ◽  
Richard J. Auchus ◽  
Michael W. Leihy ◽  
...  

The testicular androgen 5α-androstane-3α,17β-diol (androstanediol) mediates virilisation in pouch young of a marsupial, the tammar wallaby, and is the principal androgen formed in immature rodent testes. To chart the pattern of androstanediol formation in another marsupial species, the testes or fragments of testes from brushtail possums (Trichosurus vulpecula) that spanned the age range from early pouch young to mature adults were incubated with 3H-progesterone and the products were identified by high-performance liquid chromatography. The only 19-carbon steroids identified in pouch young and adult testes were the Δ4-3-keto-steroids testosterone and androstenedione. However, androstanediol and another 5α-reduced androgen (androsterone) were synthesised by testes from Day 87–200 males and these appeared to be formed from the 5α-reduction and 3-keto reduction of testosterone and androstenedione. In the prostate and glans penis of the immature male, 3H-androstanediol was converted to dihydrotestosterone. We conclude that the timing of androstanediol formation in the possum testis resembles the process in rodents rather than in the tammar wallaby and that any androstanediol in the circulation probably acts in target tissues via conversion to dihydrotestosterone.



2019 ◽  
Vol 3 (2) ◽  
pp. 122
Author(s):  
Ermi Girsang ◽  
I Nyoman Ehrich Lister ◽  
Chrismis Novalinda Ginting ◽  
Adrian Khu ◽  
Butter Samin ◽  
...  

Background: Skin aging is a condition where skin is unable to retain both its physiological and structural integrity. Plants is the main source of phtytochemicals compound with wide range of biological activities. Through the efforts of ongoing scientific researches, an increasing number of plant extracts and phytochemicals have been showed promising result as anti-aging agent. Snake fruit (Salacca zalacca (Gaert.) Voss) is tropical plant belongs to the palm tree family (Arecaceae) that served as important crop in Indonesia. Despite its utilization, the phytochemical compound available in snake fruit, especially its peel have not been well documented. Present study aimed to elucidate the phytochemical constituent of snake fruit peel and its anti-aging potency.Materials and Methods: Snake fruit peel extract (SPE) was subjected to qualitative phytochemical assay, high performance liquid chromatography, and molecular docking towards protein related in skin aging.Results: The screening showed SPE contained phytochemical compound belong to flavonoid, tannin, phenol, triterpenoid, saponin and alkaloid. Thus, based on the analysis only chlorogenic acid was present in SPE whilst rutin and caffeic acid were not detected. The SPE was contained chlorogenic acid around 1.074 mg/g dry weight. Chlorogenic acid had the high binding affinity towards matrix metalloproteinase (MMP)-1 (-9.4 kcal/mol).Conclusion: Current findings may provide scientific evidence for possible usage of SPE and its compounds as antioxidant and anti-aging agent.Keywords: Salacca zalacca, phytochemical compound, high performance liquid chromatography, anti-aging



1981 ◽  
Vol 64 (6) ◽  
pp. 1356-1363 ◽  
Author(s):  
Mary V Howell ◽  
Philip W Taylor

Abstract A sensitive, reliable, and economical method for the determination of 6 mycotoxins in mixed feeds is described. The feed is extracted with chloroform-water and the extract is cleaned up by using a disposable Sep-Pak silica cartridge. The procedure requires less time (15 min from sample extraction to extract preparation) and less solvent (approximately one-tenth) compared with conventional methods and is suitable for a fast, economical screen. Additional cleanup procedures, involving dialysis or extraction into base, are described for samples containing high levels of interfering compounds. Thin layer chromatography (TLC) and high performance liquid chromatography (HPLC) with fluorescence detection are described for identification and estimation of mycotoxins. The method has been applied to a wide range of mixed feeds, including laboratory animal diets, and raw materials. The limit of detection is 1 μg/kg for all mycotoxins measured by HPLC.



1992 ◽  
Vol 65 (2) ◽  
pp. 488-501 ◽  
Author(s):  
A. B. Sullivan ◽  
Cynthia J. Hann ◽  
George H. Kuhls

Abstract The paper reports on the sulfur vulcanization chemistry of cis-polyisoprene formulations accelerated with N-t-butyl-2-benzothiazole sulfenamide. High Performance Liquid Chromatography (HPLC) is utilized to examine the kinetics of accelerator—sulfur disappearance and the formation—disappearance profiles of extra-network cure intermediates across the vulcanization process. Cure profile measurements are reported on three formulations covering a wide range of sulfur—accelerator ratios. Also unique aspects of the analytical methodology are highlighted. The observed cure-intermediate concentration profiles reinforce earlier theories about the chemical details of sulfurization and subsequent crosslinking. On all formulations, benzothiazole polysulfides (S1−S4) reach a maximum concentration at the scorch midpoint coincident with slope changes in reactant and product profiles. Although pendant-accelerator crosslink precursors are not measured directly, their presence is implied from material balance calculations. Also, the formation of a small amount of benzothiazole early in the scorch period is a new observation in sulfenamide acceleration. It suggests that accelerator hydrolysis is a competitive side reaction early in the vulcanization process.



Soil Research ◽  
1987 ◽  
Vol 25 (2) ◽  
pp. 167 ◽  
Author(s):  
JH Watkinson ◽  
A Lee ◽  
DR Lauren

A rapid method for measuring elemental sulfur (S0) in soil and sediments is described that is accurate and precise down to a detection limit of 0.1 mg kg-l. Elemental sulfur is extracted into chloroform and measured by high-performance liquid chromatography. For moist samples, water is added to exceed their liquid limit. The method has been used to follow oxidation of both natural and fertilizer So in soil in the laboratory and field. Sediments analysed included some from lakes, and settling ponds containing coal mine wastes. Extraction within the plastic range was incomplete and recoveries as low as 5%-65% were found for five soils selected for a wide range of plastic limit. The plastic soil aggregates were not dispersed in the water-immiscible chloroform, preventing the dissolution of occluded S0; but at moisture levels above and below the plastic range, the soil was dispersed and extraction of S0 was quantitative. Extraction into a water-miscible solvent, chloroform-methanol (50 : 50), dispersed the soil at all moistures by dissolving the water thus preventing formation of plastic soil. This was less convenient because either volume correction for moisture was needed, or excess water added later to separate the chloroform. Measurement of total sulfur (S) in chloroform by inductively coupled plasma gave comparable results where samples contained S0 fertilizer, but at the lower natural levels they were much less precise and sometimes higher because of the additional S compounds extracted. Storage of moist soil below -10�C or air-dry soil at 20�C, gave no loss of S0 after one month. Moist soil at 20�C gave 40% loss after one week, but at 4�C the loss was only 5% after four weeks. Forced air-drying at 30�C, freeze-drying and microwave drying (under a narrow range of conditions) gave losses of about 5% for fertilizer S0 (<0.15 mm fraction), and of about 20% for smaller S0 crystals. In field trials with S0, sample variability was associated mostly with the difficulty of applying the S0 uniformly and with the small number of particles applied per unit area. For particles <0.25 mm, variability from mixing of cores and sub-sampling was not so great.



2020 ◽  
Vol 9 (4) ◽  
pp. 136-140
Author(s):  
A. Kh. Amandusova ◽  
K. R. Savelyeva ◽  
A. V. Morozov ◽  
V. A. Shelekhova ◽  
V. N. Shestakov ◽  
...  

Introduction. This review describes the physicochemical properties that determine the use of hyaluronic acid in ophthalmology. We have studied methods for determining hyaluronic acid using various analytical methods.Text. Hyaluronic acid is a high molecular weight glycosaminoglycan that consists of repeating disaccharides of N-acetylglucosamine and D-glucuronic acid. Carboxyl, hydroxyl and acetoamide groups give hydrophilic properties to the molecule of this anionic heteropolysaccharide. Depending on how the hyaluronic acid is obtained, its molecular weight varies over a wide range. Researchers developed methods for controlling hyaluronic acid, which include the turbidimetric titration method, the method of high-performance capillary electrophoresis and high-performance liquid chromatography and IR spectroscopic method.Conclusion. Due to its properties, hyaluronic acid is widely used as an active ingredient in pharmaceutical preparations. Today, there are a number of methods for the determination of hyaluronic acid, including the method of turbidimetric titration, the method of capillary electrophoresis. High performance liquid chromatography (HPLC) and IR spectroscopy methods are presented in the Japanese Pharmacopoeia and the European Pharmacopoeia. These techniques are widely used due to their high reproducibility, accuracy, and relative simplicity.



2017 ◽  
Vol 5 (4) ◽  
pp. 162-175
Author(s):  
Saadiyah A. Dhahir ◽  
Ameera H. Hamed

Honey is rich in phenolic acids and flavonoids, which exhibit a wide range of biological effects and act as natural antioxidants. The analysis of polyphenols has been regarded as a very promising way of studying floral and geographical origins of honeys. The aim of this study was to determine, flavonoid in honey samples collected from different region in Iraq and Comparison with others kind. The flavonoids which measured in honey samples are (Myricetin, Quercetin, Hesperdin, Naringenin, Apigenin, Kaempferol, Chrisin). Chromatographic Separation was performed using a reversed phase column C18 and acetonitrile 60% (v/v) flow rate 1.0 ml/min, pH 5.5 at 280 nm. All calibration curves of the flavonoid compounds showed good linearity   (r -0.9999) within the test range. Concentration of flavonoids ranged from Myricetin (1.903- 18.5) mg/kg, Quercetin (3.31-22.01) mg/kg, Hesperdin (4.55-16.2) mg/kg, Naringenin (3.2-24.68) mg/kg, Apigenin (6.76-28.81) mg/kg, Kaempferol (3.31-38.13) mg/kg, Chrisin (2.0-28.0) mg/kg respectively.



2021 ◽  
Vol 2 (3) ◽  
pp. 155-158
Author(s):  
Mahsa Hasanzadeh ◽  
◽  
Amir Heydari ◽  

AIM: To evaluate the levofloxacin eye drop into human eye penetration, levofloxacin eye drop concentrations in human ocular aqueous of 33 patients undergoing cataract surgery were measured by high performance liquid chromatography (HPLC). METHODS: Totally 33 volunteer patients who scheduled for phacoemulsification surgery received one drop of levofloxacin every 6h for 3d before and on the day of surgery, administration of drug was stopped 1h before surgery. Levofloxacin concentration in aqueous humor was measured by HPLC method with fluorescence detector. RESULTS: A simple, effective and sensitive HPLC method for determination of levofloxacin in human ocular aqueous was validated. Linearity was shown for levofloxacin concentration over a wide range of 1.95×10-3-1.50 µg/mL. The mean aqueous level of levofloxacin was 0.3399±0.03405 µg/mL. CONCLUSION: Results from the present study demonstrate that topical administration of levofloxacin 0.5% before cataract surgery with routine dose (one drop every 6h) unable to reach MIC90 for most common microorganism causing acute bacterial endophthalmitis.



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