scholarly journals Effects of the Artificial Culture Medium of Wild Ginsengs on Rumen Fermentation Characteristics In Vitro

2003 ◽  
Vol 45 (6) ◽  
pp. 987-996 ◽  
Keyword(s):  
Culture Medium ◽  
Rumen Fermentation ◽  
Artificial Culture ◽  
Artificial Culture Medium

scholarly journals A novel experimental approach for studying life-history traits of phytophagous arthropods utilizing an artificial culture medium

2019 ◽  
Vol 9 (1) ◽  
Author(s):  
Kamila Karpicka-Ignatowska ◽  
Alicja Laska ◽  
Lechosław Kuczyński ◽  
Brian G. Rector ◽  
Mariusz Lewandowski ◽  
...  
Keyword(s):  
Life History ◽  
Host Plant ◽  
Life History Traits ◽  
Culture Medium ◽  
Interspecific Interactions ◽  
Suitable Condition ◽  
Mite Species ◽  
Artificial Culture ◽  
Wide Range ◽  
Artificial Culture Medium

AbstractExperimental approaches to studying life-history traits in minute herbivorous arthropods are hampered by the need to work with detached host plant material and the difficulty of maintaining that material in a suitable condition to support the animal throughout the duration of the test. In order to address this shortcoming, we developed a customizable agar-based medium modified from an established plant cell-culture medium to nourish detached leaves laid atop it while also preventing arthropods from escaping the experimental arena. The artificial culture medium was tested with two herbivorous mite species: the wheat curl mite (Aceria tosichella; Eriophyidae) and two-spotted spider mite (Tetranychus urticae; Tetranychidae). The proposed approach was a major improvement over a standard protocol for prolonged studies of individual eriophyid mites and also provided some benefits for experiments with spider mites. Moreover, the described method can be easily modified according to the requirements of host plant species and applied to a wide range of microherbivore species. Such applications include investigations of life-history traits and other ecological and evolutionary questions, e.g. mating or competitive behaviours or interspecific interactions, assessing invasiveness potential and predicting possible outbreaks. The approach presented here should have a significant impact on the advancement of evolutionary and ecological research on microscopic herbivores.

scholarly journals Design of an artificial culture medium to optimize Haslea ostrearia biomass and marennine production

2020 ◽  
Vol 45 ◽  
pp. 101653 ◽  
Author(s):  
R. Nghiem Xuan ◽  
I. Safitri ◽  
J.L. Mouget ◽  
J. Pruvost ◽  
V. Turpin ◽  
...  
Keyword(s):  
Culture Medium ◽  
Artificial Culture ◽  
Haslea Ostrearia ◽  
Artificial Culture Medium

Follicle-stimulating hormone-dependent estrogen secretion by rat Sertoli cells in vitro: Modulation by calcium

1991 ◽  
Vol 125 (3) ◽  
pp. 280-285 ◽  
Author(s):  
J. Alan Talbot ◽  
Ann Lambert ◽  
Robert Mitchell ◽  
Marek Grabinski ◽  
David C. Anderson ◽  
...  
Keyword(s):  
Sertoli Cells ◽  
Culture Medium ◽  
Follicle Stimulating Hormone ◽  
Dibutyryl Camp ◽  
Immature Rat ◽  
Estradiol Secretion ◽  
Old Rats ◽  
Stimulating Hormone

Abstract We have investigated the role of Ca2+ in the control of FSH-induced estradiol secretion by Sertoli cells isolated from 8-10 days old rats. Exogenous Ca2+ (4-8 mmol/1) inhibited FSH-stimulated E2 secretion such that, with 8 mmol/l Ca2+ and FSH (8 IU/l) E2 secretion decreased from 2091±322 to 1480±84 pmol/l (p<0.002), whilst chelation of Ca2+ in the culture medium with EGTA (3 mmol/l) increased E2 secretion from 360±45 to 1242±133 pmol/l) in the absence of FSH. Further, EGTA (3 mmol/l) markedly potentiated FSH (8 IU/l), forskolin (1 μmol/l) and dibutyryl cAMP (1 mmol/l)-stimulated E2 secretion. Addition of the Ca2+ ionophores, ionomycin (2-5 μmol/l) and A23187 (2 μmol/l), inhibited FSH (8 IU/l)-stimulated E2 secretion by >80%. The effect of ionomycin was totally reversible, whereas that of A23187 was irreversible. Ionomycin (5 μmol/l) had no effect on EGTA-induced E2 secretion in the absence of FSH, but reduced EGTA-provoked E2 secretion by 59% in the presence of FSH (8 IU/l). Similarly, forskolin- and dibutyryl cAMP-provoked E2 production was inhibited 46-50% by ionomycin (5 μmol/l). We conclude that FSH-induced E2 secretion from immature rat Sertoli cells is modulated by intra- and extracellular Ca2+.

Pulsatile GnRH secretion from primary cultures of sheep olfactory placode explants

Reproduction ◽  
2000 ◽  
pp. 391-396 ◽  
Author(s):  
AH Duittoz ◽  
M Batailler
Keyword(s):  
Culture Medium ◽  
Primary Cultures ◽  
Pulsatile Secretion ◽  
Olfactory Placode ◽  
Gnrh Secretion ◽  
Individual Culture ◽  
Pulsatile Gnrh

The aim of this study was to investigate the development of pulsatile GnRH secretion by GnRH neurones in primary cultures of olfactory placodes from ovine embryos. Culture medium was collected every 10 min for 8 h to detect pulsatile secretion. In the first experiment, pulsatile secretion was studied in two different sets of cultures after 17 and 24 days in vitro. In the second experiment, a set of cultures was tested after 10, 17 and 24 days in vitro to investigate the development of pulsatile GnRH secretion in each individual culture. This study demonstrated that (i) primary cultures of GnRH neurones from olfactory explants secreted GnRH in a pulsatile manner and that the frequency and mean interpulse duration were similar to those reported in castrated ewes, and (ii) pulsatile secretion was not present at the beginning of the culture but was observed between 17 and 24 days in vitro, indicating the maturation of individual neurones and the development of their synchronization.

1642 Effect of Enterococcus fecalis SROD5 supplementation on microbial communities and quantities of in vitro rumen fermentation

2016 ◽  
Vol 94 (suppl_5) ◽  
pp. 800-800
Author(s):  
L. L. Mamuad ◽  
S. S. Lee ◽  
A. A. Biswas ◽  
C. D. Jeong
Keyword(s):  
Microbial Communities ◽  
Rumen Fermentation ◽  
In Vitro Rumen Fermentation

Reprogrammed M1 macrophages with inhibited STAT3, STAT6 and/or SMAD3 extends lifespan of mice with experimental carcinoma

2017 ◽  
pp. 4-9
Author(s):  
С.В. Калиш ◽  
С.В. Лямина ◽  
А.А. Раецкая ◽  
И.Ю. Малышев
Keyword(s):  
Tumor Growth ◽  
Culture Medium ◽  
Ehrlich Carcinoma ◽  
Macrophage Phenotype ◽  
M1 Macrophages ◽  
M1 Macrophage ◽  
Ec Cells ◽  
Experimental Carcinoma

Цель исследования. Репрограммирование М1 фенотипа макрофагов с ингибированными факторами транскрипции М2 фенотипа STAT3, STAТ6 и SMAD и оценка их влияния на развитие карциномы Эрлиха (КЭ) in vitro и in vivo. Методика. Рост опухоли иницировали in vitro путем добавления клеток КЭ в среду культивирования RPMI-1640 и in vivo путем внутрибрюшинной инъекции клеток КЭ мышам. Результаты. Установлено, что M1макрофаги и in vitro, и in vivo оказывают выраженный противоопухолевый эффект, который превосходит антиопухолевые эффекты М1, M1, M1 макрофагов и цисплатина. Заключение. М1 макрофаги с ингибированными STAT3, STAT6 и/или SMAD3 эффективно ограничивают рост опухоли. Полученные данные обосновывают разработку новой технологии противоопухолевой клеточной терапии. Objective. Reprogramming of M1 macrophage phenotype with inhibited M2 phenotype transcription factors, such as STAT3, STAT6 and SMAD and assess their impact on the development of Ehrlich carcinoma (EC) in vitro and in vivo . Methods. Tumor growth in vitro was initiated by addition of EC cells in RPMI-1640 culture medium and in vivo by intraperitoneal of EC cell injection into mice. Results. It was found that M1 macrophages have a pronounced anti-tumor effect in vitro , and in vivo , which was greater than anti-tumor effects of M1, M1, M1 macrophages and cisplatin. Conclusion. M1 macrophages with inhibited STAT3, STAT6 and/or SMAD3 effectively restrict tumor growth. The findings justify the development of new anti-tumor cell therapy technology.

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