scholarly journals Screening of the Active Component Promoting Leydig Cell Proliferation from Lepidium meyenii Using HPLC-ESI-MS/MS Coupled with Multivariate Statistical Analysis

Molecules ◽  
2019 ◽  
Vol 24 (11) ◽  
pp. 2101 ◽  
Author(s):  
Xiao-chen Gao ◽  
Jing-wei Lv ◽  
Chun-nan Li ◽  
Nan-xi Zhang ◽  
Lin-lin Tian ◽  
...  
Keyword(s):  
Cell Proliferation ◽  
Leydig Cell ◽  
Active Sites ◽  
Docking Simulation ◽  
Cyclophilin D ◽  
Quick Method ◽  
Specific Chemical ◽  
Hplc Fingerprint ◽  
Lepidium Meyenii ◽  
Testosterone Secretion

Lepidium meyenii is now widely consumed as a functional food and medicinal product, which is known as an enhancer of reproductive health. However, the specific chemical composition and mechanism of action for improving sexual function are unclear. The present study aims at screening and determining the potential compounds, which promote mouse leydig cells (TM3) proliferation. The partial least squares analysis (PLS) was employed to reveal the correlation between common peaks of high performance liquid chromatography (HPLC) fingerprint of L. meyenii and the proliferation activity of TM3. The results suggested that three compounds had good activities on the proliferation of TM3 and promoting testosterone secretion, there were N-benzyl-hexadecanamide, N-benzyl-(9z,12z)-octadecadienamide and N-benzyl-(9z,12z,15z)-octadecatrienamide which might be the potential bioactive markers related to the enhancing sexual ability functions of L. meyenii. The first step in testosterone synthesis is the transport of cholesterol into the mitochondria, and the homeostasis of mitochondrial function is related to cyclophilin D (CypD). In order to expound how bioactive ingredients lead to promoting testosterone secretion, a molecular docking simulation was used for further illustration in the active sites and binding degree of the ligands on CypD. The results indicated there was a positive correlation between the binding energy absolute value and testosterone secretion activity. In addition, in this study it also provided the reference for a simple, quick method to screen the promoting leydig cell proliferation active components in traditional Chinese medicine (TCM).

scholarly journals Endocrine Disruptors Differentially Target ATP-Binding Cassette Transporters in the Blood-Testis Barrier and Affect Leydig Cell Testosterone Secretion In Vitro

2013 ◽  
Vol 136 (2) ◽  
pp. 382-391 ◽  
Author(s):  
Anita C. A. Dankers ◽  
Maarke J. E. Roelofs ◽  
Aldert H. Piersma ◽  
Fred C. G. J. Sweep ◽  
Frans G. M. Russel ◽  
...  
Keyword(s):  
Endocrine Disruptors ◽  
Leydig Cell ◽  
Atp Binding ◽  
Testosterone Secretion ◽  
Atp Binding Cassette Transporters ◽  
Blood Testis Barrier ◽  
Atp Binding Cassette

scholarly journals Conazole fungicides inhibit Leydig cell testosterone secretion and androgen receptor activation in vitro

2014 ◽  
Vol 1 ◽  
pp. 271-283 ◽  
Author(s):  
Maarke J.E. Roelofs ◽  
A. Roberto Temming ◽  
Aldert H. Piersma ◽  
Martin van den Berg ◽  
Majorie B.M. van Duursen
Keyword(s):  
Androgen Receptor ◽  
Leydig Cell ◽  
Receptor Activation ◽  
Testosterone Secretion ◽  
Androgen Receptor Activation

scholarly journals Structural Basis of Binding and Rationale for the Potent Urease Inhibitory Activity of Biscoumarins

2014 ◽  
Vol 2014 ◽  
pp. 1-12 ◽  
Author(s):  
Muhammad Arif Lodhi ◽  
Sulaiman Shams ◽  
Muhammad Iqbal Choudhary ◽  
Atif Lodhi ◽  
Zaheer Ul-Haq ◽  
...  
Keyword(s):  
Molecular Docking ◽  
Active Sites ◽  
Docking Simulation ◽  
Cysteine Residue ◽  
Structural Basis ◽  
Bacillus Pasteurii ◽  
Nickel Ions ◽  
Jack Bean ◽  
Uv Visible

Urease belongs to a family of highly conserved urea-hydrolyzing enzymes. A common feature of these enzymes is the presence of two Lewis acid nickel ions and reactive cysteine residue in the active sites. In the current study we examined a series of biscoumarins1–10for their mechanisms of inhibition with the nickel containing active sites of Jack bean andBacillus pasteuriiureases. All these compounds competitively inhibited Jack bean urease through interaction with the nickel metallocentre, as deduced from Michaelis-Menten kinetics, UV-visible absorbance spectroscopic, and molecular docking simulation studies. Some of the compounds behaved differently in case ofBacillus pasteuriiurease. We conducted the enzyme kinetics, UV-visible spectroscopy, and molecular docking results in terms of the known protein structure of the enzyme. We also evaluated possible molecular interpretations for the site of biscoumarins binding and found that phenyl ring is the major active pharmacophore. The excellent in vitro potency and selectivity profile of the several compounds described combined with their nontoxicity against the human cells and plants suggest that these compounds may represent a viable lead series for the treatment of urease associated problems.

THE INFLUENCE OF OVERCROWDING ON SPERMATOGENESIS, SIZE OF LEYDIG-CELL NUCLEI (HISTOMETRICAL INVESTIGATION), AND THE ADRENAL CORTICOSTERONE CONTENTS IN MICE

1973 ◽  
Vol 74 (4) ◽  
pp. 783-791 ◽  
Author(s):  
K. Gärtner ◽  
H. Reznik-Schüller ◽  
G. Reznik
Keyword(s):  
Population Size ◽  
Group Size ◽  
Adult Male ◽  
Leydig Cell ◽  
Relative Frequency ◽  
Seminiferous Tubules ◽  
Cell Nuclei ◽  
Nmri Mice ◽  
Testosterone Secretion ◽  
Adrenal Corticosterone

ABSTRACT Adult male NMRI-mice were kept alone or in groups of 5, 10, 20, 30, 40 and 60 animals for 28 days and were then sacrificed. The corticosterone levels of their adrenals were determined and their testes were examined histometrically. The corticosterone levels of the adrenals increased two-fold with increasing population size. Furthermore the increased population size caused a suppression of some testicular functions: the seminiferous tubules decreased up to 20 % and the relative frequency of the spermatids up to 10 % whereas the numbers of spermatocytes and spermatogonias increased correspondingly. A decrease of about 25 % of the testosterone dependent postmeiotic stages of spermatogenesis is assumed. Since the diameters of the Leydig-cell nuclei decreased about 20 %, a reduction of the testicular testosterone secretion can be projected. All measurements proved the group with 5 animals to be the most favourable group size.

scholarly journals Mumps Virus Decreases Testosterone Production and Gamma Interferon-Induced Protein 10 Secretion by Human Leydig Cells

2003 ◽  
Vol 77 (5) ◽  
pp. 3297-3300 ◽  
Author(s):  
Ronan Le Goffic ◽  
Thomas Mouchel ◽  
Annick Ruffault ◽  
Jean-Jacques Patard ◽  
Bernard Jégou ◽  
...  
Keyword(s):  
Cell Cultures ◽  
Leydig Cell ◽  
Leydig Cells ◽  
Mumps Virus ◽  
Gamma Interferon ◽  
Testosterone Secretion ◽  
Testosterone Production

ABSTRACT Mumps virus is responsible for sterility. Here, we show that the mumps virus infects Leydig cells in vitro and totally inhibits testosterone secretion and that ribavirin in mumps virus-infected Leydig cell cultures completely restores testosterone production. Moreover, we show that gamma interferon-induced protein 10 (IP-10) is highly expressed by mumps virus-infected Leydig cells and that ribavirin does not block IP-10 production.

Testosterone Secretion by Rat, Rabbit, Guinea Pig, Dog, and Hamster Testes Perfused in Vitro: Correlation with Leydig Cell Mass*

Endocrinology ◽  
1979 ◽  
Vol 105 (5) ◽  
pp. 1135-1142 ◽  
Author(s):  
L. L. EWING ◽  
B. R. ZIRKIN ◽  
R. C. COCHRAN ◽  
N. KROMANN ◽  
C. PETERS ◽  
...  
Keyword(s):  
Guinea Pig ◽  
Leydig Cell ◽  
Cell Mass ◽  
Testosterone Secretion

Effects of melatonin treatment on Leydig cell activity in the testis of the frog Rana esculenta

Zygote ◽  
2004 ◽  
Vol 12 (4) ◽  
pp. 293-299 ◽  
Author(s):  
Michela d'Istria ◽  
Ismene Serino ◽  
Gaia Izzo ◽  
Diana Ferrara ◽  
Gianluca De Rienzo ◽  
...  
Keyword(s):  
Leydig Cell ◽  
Leydig Cells ◽  
Morphological Changes ◽  
Cell Activity ◽  
Rana Esculenta ◽  
Cellular Adhesion ◽  
Morphological Observation ◽  
Melatonin Treatment ◽  
Testosterone Secretion

This study was conducted to verify the effect(s) of melatonin treatment on frog Leydig cells. Morphological observation after melatonin treatment indicates that many frog Leydig cells show degenerative changes (i.e. heterochromatic nuclei, loss of cellular adhesion) while in adjacent germinal tubules several Sertoli cells show heterochromatic nuclei, confirming the presence of a paracrine effect between interstitial and germinal compartments. The effect of melatonin on frog Leydig cell steroidogenesis was investigated in in vitro experiments; after 6 h of incubation melatonin severely inhibits both control and GnRH-induced testosterone secretion. In addition, in order to verify the effect of indolamine on frog Leydig cell activity, we investigated, by in situ hybridization, the presence of frog relaxin (fRLX, a transcript specifically expressed by these cells) in the testes of melatonin-injected animals after 48 h. fRLX signal completely disappeared from the testis of melatonin-injected frogs. The results of the present study indicate that melatonin treatment provokes Leydig cell morphological changes, blocks GnRH-antagonist-induced testosterone secretion and decreases fRLX expression. Taken together these results strongly indicate that melatonin acts on Leydig cells in the testis of the frog Rana esculenta.

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