scholarly journals PSIV-9 Effects of polyamines and trenbolone acetate on proliferation rates of murine myoblasts

2020 ◽  
Vol 98 (Supplement_4) ◽  
pp. 287-288
Author(s):  
Laura A Smith ◽  
Nikole E Ineck ◽  
Brynne A Udy ◽  
Chris L Erickson ◽  
Kara J Thornton
Keyword(s):  
Skeletal Muscle ◽  
Bovine Serum ◽  
Biosynthetic Pathway ◽  
Fetal Bovine Serum ◽  
Muscle Growth ◽  
C2c12 Cells ◽  
Trenbolone Acetate ◽  
Skeletal Muscle Growth ◽  
Fetal Bovine ◽  
The Relationship

Abstract Androgens, such as testosterone, increase growth of skeletal muscle, although the exact mechanism through which these molecules function to increase growth of skeletal muscle remains unknown. Recent research indicates that one of the mechanisms through which androgens improve skeletal muscle growth is by modulation of the polyamine biosynthetic pathway. Polyamines are naturally occurring amino acid derivatives that are found in many whole foods and are potent stimulators of cell proliferation. However, the effect that polyamines have on growth of skeletal muscle has not been well characterized. The objective of this study was to investigate the effect that trenbolone acetate (a testosterone analog, TBA), polyamines (putrescine, spermine, and spermidine), and polyamine precursors (methionine and ornithine) have on proliferation of Sol8 and C2C12 murine myoblasts. Cultures were treated with 1% fetal bovine serum and 10 nM TBA, 10 mM methionine, 8 mM ornithine, 3 mM putrescine, 1.5 mM spermidine, or 0.1 mM spermine and proliferation rates were compared to a control (1% fetal bovine serum). Sol8 cells that were treated with 10 nM TBA, 10 mM methionine, 8 mM ornithine, 3 mM putrescine, 1.5 mM spermidine, or 0.1 mM spermine had increased (P < 0.05) proliferation rates compared to the control. C2C12 cells that were treated with 10 nM TBA or 10 mM methionine had increased (P < 0.05) proliferation rates compared to the control. This research demonstrates that TBA, some polyamines, and some polyamine precursors increase proliferation of myoblasts and thus, are capable of enhancing the rate of skeletal muscle growth. However, further research is needed to understand the relationship between androgens and the polyamine biosynthetic pathway relative to skeletal muscle growth.

scholarly journals PSII-8 Effects of polyamines and trenbolone acetate on proliferation rates of murine myoblasts

2019 ◽  
Vol 97 (Supplement_3) ◽  
pp. 234-234
Author(s):  
Laura A Smith ◽  
Nikole E Ineck ◽  
Brynne A Udy ◽  
Chris L Erickson
Keyword(s):  
Skeletal Muscle ◽  
Bovine Serum ◽  
Biosynthetic Pathway ◽  
Fetal Bovine Serum ◽  
Muscle Growth ◽  
Cell Types ◽  
C2c12 Cells ◽  
Trenbolone Acetate ◽  
Skeletal Muscle Growth ◽  
Fetal Bovine

Abstract Androgens, such as testosterone, increase growth of skeletal muscle, although the exact mechanism through which these molecules function to increase growth of skeletal muscle remains unknown. Recent research indicates that one of the mechanisms through which androgens improve skeletal muscle growth is by modulation of the polyamine biosynthetic pathway. Polyamines are naturally occurring amino acid derivatives that are found in many whole foods and are potent stimulators of cell proliferation in several different cell types. However, the effect that polyamines have on growth of skeletal muscle has not been well characterized. The objective of this study was to investigate the effect that trenbolone acetate (a testosterone analog, TBA), polyamines (putrescine, spermine, and spermidine), and polyamine precursors (methionine and ornithine) have on proliferation of Sol8 and C2C12 murine myoblasts. Cultures were treated with 1% fetal bovine serum and 10 nM TBA, 10 mM methionine, 8 mM ornithine, 3 mM putrescine, 1.5 mM spermidine, or 0.5 mM spermine and proliferation rates were compared to a control (1% fetal bovine serum). Sol8 cells that were treated with 10 nM TBA and 10 mM methionine had increased (P < 0.001) proliferation rates compared to the control. C2C12 cells that were treated with 10 nM TBA, 8 mM ornithine, or 1.5 mM spermidine had increased (P < 0.001) proliferation rates compared to the control. This research demonstrates that TBA, some polyamines, and some polyamine precursors increase proliferation of myoblasts and thus, are capable of enhancing the rate of skeletal muscle growth. However, further research is needed to understand the relationship between androgens and the polyamine biosynthetic pathway relative to skeletal muscle growth.

scholarly journals PSI-15 Determining the molecular mechanism through which estradiol and trenbolone acetate improve skeletal muscle growth in beef cattle

2019 ◽  
Vol 97 (Supplement_3) ◽  
pp. 293-293
Author(s):  
Caleb C Reichhardt ◽  
Chris A Bidwell ◽  
Aaron Thomas ◽  
Amir Ahmadpour
Keyword(s):  
Skeletal Muscle ◽  
Beef Cattle ◽  
Molecular Mechanism ◽  
Muscle Growth ◽  
Specific Inhibitor ◽  
Growth Efficiency ◽  
The United States ◽  
Trenbolone Acetate ◽  
Skeletal Muscle Growth ◽  
Future Work

Abstract Approximately 90% of beef cattle on feed in the United States receive an anabolic implant during production, which results in increased growth, efficiency, and economic return to producers. However, the molecular mechanism through which these anabolic implants operate to improve skeletal muscle growth remains unknown. The objective of this study was to determine the molecular mechanism through which estradiol (E2) and trenbolone acetate (TBA) improve skeletal muscle growth in beef cattle and to specifically understand whether E2 and/or TBA function by modulating transcription. To address this, bovine satellite cells (BSC) were isolated from three different backgrounded steers and grown in culture. Once cultures reached 75% confluency they were treated with 1% fetal bovine serum (FBS) and 10 nM E2 or 10 nM TBA. In an additional experiment, all previously listed treatments were given in addition to actinomycin D (AD, a non-specific inhibitor of transcription). Treatment with E2 or TBA increased proliferation (P < 0.05) when compared to a 1% FBS control. Furthermore, treatment with E2 or TBA in the presence of AD increased proliferation (P < 0.01) when compared to cultures treated with just AD. These results indicate that TBA and E2 are both capable of increasing proliferation of BSC cultures through non-transcriptional mechanisms. Future work will identify the TBA and E2 signaling pathways that affect muscle growth and don’t involve changes in gene transcription.

scholarly journals Phytochemicals in Chinese chive (Allium tuberosum) Induce the Skeletal Muscle Cell Proliferation via PI3K/Akt/mTOR and Smad Pathways in C2C12 Cells

2021 ◽  
Vol 22 (5) ◽  
pp. 2296
Author(s):  
Mira Oh ◽  
Seo-Young Kim ◽  
SeonJu Park ◽  
Kil-Nam Kim ◽  
Seung Hyun Kim
Keyword(s):  
Skeletal Muscle ◽  
Cell Proliferation ◽  
Muscle Cell ◽  
Muscle Growth ◽  
Skeletal Muscle Cell ◽  
Water Soluble ◽  
C2c12 Cells ◽  
Allium Tuberosum ◽  
Skeletal Muscle Growth ◽  
Chinese Chive

Chinese chive (Allium tuberosum) is a medicinal food that is cultivated and consumed mainly in Asian countries. Its various phytochemicals and physiological effects have been reported, but only a few phytochemicals are available for skeletal muscle cell proliferation. Herein, we isolated a new compound, kaempferol-3-O-(6″-feruloyl)-sophoroside (1), along with one known flavonoid glycoside (2) and six amino acid (3–8) compounds from the water-soluble fraction of the shoot of the Chinese chive. The isolated compounds were identified using extensive spectroscopic methods, including 1D and 2D NMR, and evaluated for their proliferation activity on skeletal muscle cells. Among the tested compounds, newly isolated flavonoid (1) and 5-aminouridine (7) up-regulated PI3K/Akt/mTOR pathways, which implies a positive effect on skeletal muscle growth and differentiation. In particular, compound 1 down-regulated the Smad pathways, which are negative regulators of skeletal muscle growth. Collectively, we suggest that major constituents of Chinese chive, flavonoids and amino acids, might be used in dietary supplements that aid skeletal muscle growth.

Altered mRNA abundance of ASB15 and four other genes in skeletal muscle following administration of β-adrenergic receptor agonists

2004 ◽  
Vol 16 (2) ◽  
pp. 275-283 ◽  
Author(s):  
Tara G. McDaneld ◽  
Deana L. Hancock ◽  
Diane E. Moody
Keyword(s):  
Skeletal Muscle ◽  
Adrenergic Receptor ◽  
Muscle Growth ◽  
Differentially Expressed Gene ◽  
Differentially Expressed ◽  
Female Rats ◽  
Trenbolone Acetate ◽  
Receptor Agonists ◽  
Skeletal Muscle Growth ◽  
Downstream Signaling

β-Adrenergic receptor agonists (BA) stimulate skeletal muscle growth. However, downstream signaling pathways that facilitate this effect remain poorly defined. Objectives of this study were to identify genes differentially expressed after administration of a novel BA and to evaluate the expression of one of those genes in additional models of skeletal muscle growth. Differentially expressed gene fragments were identified through differential display of skeletal muscle biopsies from five steers 24 h after administration of the BA. Five gene fragments designated DD53, DD143, DD163, DD209, and DD214 were identified. Tissue distribution of these genes was evaluated by RT-PCR. While DD53, DD163, DD209, and DD214 were expressed across tissues, DD143 mRNA expression was most abundant in skeletal muscle. DD143, later identified as bovine ASB15, was evaluated in rats following administration of anabolic compounds. Thirteen 7-wk-old female rats were randomly assigned to each of four treatment groups including: control, clenbuterol, trenbolone acetate (TBA), and growth hormone (GH). Changes in rat Asb-15 mRNA were measured at 30 min, 12 h, and 24 h following intraperitoneal injections of each compound. Clenbuterol treatment decreased Asb-15 mRNA in skeletal muscle at 12 and 24 h ( P < 0.01) and also decreased mRNA in lung at 12 h ( P < 0.05). TBA and GH treatments did not alter Asb-15 mRNA in any of the tissues evaluated ( P > 0.10). These results are the first to associate an Asb gene family member with muscle growth or BA administration and suggest a potential role for ASB15 in β-agonist-induced skeletal muscle hypertrophy.

Treatment of fetal bovine serum improves early development of porcine embryos by alleviating oxidative stress

2014 ◽  
Author(s):  
Seon-A Choi ◽  
Seong-Eun Mun ◽  
Pil-Soo Jeong ◽  
Hae-Jun Yang ◽  
Seung-Bin Yoon ◽  
...  
Keyword(s):  
Oxidative Stress ◽  
Early Development ◽  
Bovine Serum ◽  
Fetal Bovine Serum ◽  
Fetal Bovine

МОДЕЛИРОВАНИЕ СИСТЕМ ЭКСТРАКОРПОРАЛЬНОГО СОЗРЕВАНИЯ ООЦИТОВ КРУПНОГО РОГАТОГО СКОТА С ИСПОЛЬЗОВАНИЕМ СТРУКТУРНЫХ КОМПОНЕНТОВ ОВАРИАЛЬНЫХ ФОЛЛИКУЛОВ *

2019 ◽  
pp. 20-22
Author(s):  
T.I. KUZMINA ◽  
I.V. CHISTYAKOVA
Keyword(s):  
Granulosa Cells ◽  
Follicular Fluid ◽  
Bovine Serum ◽  
Egg Quality ◽  
Fetal Bovine Serum ◽  
Reproductive Technologies ◽  
Blastocyst Stage ◽  
Preimplantation Embryos ◽  
Cultural Systems ◽  
Fetal Bovine

Создание эффективной унифицированной системы дозревания донорских ооцитов обеспечит повышение результативности инновационных клеточных репродуктивных технологий. В исследовании проведен сравнительный мониторинг показателеймейотического созревания ооцитов коров, созревших в различных системах, дополненных структурными компонентами фолликулов (СКФ стенки фолликулов, клетки гранулезы, белки) и фолликулярной жидкостью,а также потенций к развитию из них доимплантационных эмбрионов. Анализу подверглись ооциты, прокультивированные в следующих системах:среда ТС199 с добавлением 10 фетальной бычьей сыворотки (ФБС), 50 мкг/мл эстрадиола, 10 мкг/мл лютеинизирующего гормона (ЛГ), 10 мкг/мл фолликулостимулирующего гормона (ФСГ) среда ТС199 с 10 эстральной сывороткой коров среда ТС199 с 50 жидкости из фолликулов диаметром 9 мм среда ТС199 с добавлением белков фолликулярной жидкости молекулярной массой 65 кДасреда ТС199 с 10 ФБС и 1106 клеток гранулезы среда ТС199 с 10 ФБС и тканью фолликула. В культуральные среды ко всем исследованным группам ооцитов добавляли антибиотики. Использование CКФ обеспечило значительное снижение доли ооцитов с дегенерированным хроматином, что способствовало увеличению уровня доимпланационных эмбрионов на стадии бластоцисты. Так, доля бластоцист, развившихся из ооцитов, созревших в среде со стенками фолликулов,составила43,5. В этой же группе выявлен минимальный уровень дегенерированных зародышей (6,45). Полученные данные предлагается использовать при моделировании систем дозревания ооцитов коров с целью повышения качества яйцеклеток.The creation of an effective unified maturation system of donor oocytes provides an increase in the efficiency of innovative cellular reproductive technologies. The comparative analysis of the meiotic maturation indicators of bovine oocytes, which were matured in different cultural systems modified by follicular structural components (FSC follicular walls, granulosa cells, proteins) and follicular fluid, as well as the potential for preimplantation embryonic development were evaluated in this study. Oocytes matured in following cultural systems: medium TC199 supplemented with 10 fetal bovine serum and 50 g/ml of estradiol, 10 g/ml of luteinizing hormone (LH), 10 g/ml of folliclestimulating hormone (FSH) medium TC199 with 10 estrous cow serum medium TC199 with 50 liquid from follicles with a diameter of 9 mm medium TC199 supplemented with the follicular fluid proteins with molecular weight 65 kDa medium TC199 with 10 fetal bovine serum and 1106 granulosa cells medium TC199 with the addition of 10 fetal bovine serum and follicle tissues were analyzed. Antibiotics were added to cultural media of all experimental groups of oocytes. The usage of FSC ensured the decrease in the proportion of oocytes with degenerated chromatin, which contribute the rise of the level of preimplantation embryos at the blastocyst stage. Thus, the proportion of blastocysts developed from oocytes matured in medium supplemented with follicular walls was 43.5. In the same experimental group, the number of degenerated embryos was 6.45. The obtained data are supposed to be used for modeling the cultural systems of cow oocytes in order to improve the egg quality.

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