Isomer-specific accumulation of perfluorooctane sulfonate in the liver of chicken embryos exposed in ovo to a technical mixture

2010 ◽  
Vol 30 (1) ◽  
pp. 226-231 ◽  
Author(s):  
Jason M. O'Brien ◽  
Sean W. Kennedy ◽  
Shaogang Chu ◽  
Robert J. Letcher
Keyword(s):  
Perfluorooctane Sulfonate ◽  
In Ovo ◽  
Chicken Embryos ◽  
Specific Accumulation ◽  
Technical Mixture

scholarly journals Silver Nanoparticles as Modulators of Myogenesis-Related Gene Expression in Chicken Embryos

Genes ◽  
2021 ◽  
Vol 12 (5) ◽  
pp. 629
Author(s):  
Walaa A. Husseiny ◽  
Abeer A. I. Hassanin ◽  
Adel A. S. El Nabtiti ◽  
Karim Khalil ◽  
Ahmed Elaswad
Keyword(s):  
Silver Nanoparticles ◽  
Placebo Treatment ◽  
Cellular Level ◽  
Breast Muscle ◽  
Transcriptional Level ◽  
Poultry Production ◽  
In Ovo ◽  
Chicken Embryos ◽  
Muscle Tissues ◽  
Myogenic Factor

The present study was conducted to investigate the effects of colloidal nanoparticles of silver (Nano-Ag) on the expression of myogenesis-related genes in chicken embryos. The investigated genes included the members of the myogenic regulatory factors family (MRFs) and myocyte enhancer factor 2A (MEF2A) genes. A total of 200 fertilized broiler eggs (Indian River) were randomly distributed into four groups; non-injected control, injected control with placebo, treatment I in ovo injected with 20 ppm Nano-Ag, and treatment II in ovo injected with 40 ppm Nano-Ag. The eggs were then incubated for 21 days at the optimum temperature and humidity conditions. Breast muscle tissues were collected at the 5th, 8th, and 18th days of the incubation period. The mRNA expression of myogenic determination factor 1 (MYOD1), myogenic factor 5 (MYF5), myogenic factor 6 (MYF6), myogenin (MYOG), and MEF2A was measured at the three sampling points using real-time quantitative PCR, while MYOD1 protein expression was evaluated on day 18 using western blot. Breast muscle tissues were histologically examined on day 18 to detect the changes at the cellular level. Our results indicate that myogenesis was enhanced with the low concentration (20 ppm) of Nano-Ag due to the higher expression of MYOD1, MYF5, and MYF6 at the transcriptional level and MYOD1 at the translational level. Moreover, histological analysis revealed the presence of hyperplasia (31.4% more muscle fibers) in treatment I (injected with 20 ppm). Our findings indicate that in ovo injection of 20 ppm Nano-Ag enhances the development of muscles in chicken embryos compared with the 40-ppm dosage and provide crucial information for the use of silver nanoparticles in poultry production.

Development of specific muscle and cutaneous sensory projections in cultured segments of spinal cord

Development ◽  
1994 ◽  
Vol 120 (5) ◽  
pp. 1315-1323 ◽  
Author(s):  
K. Sharma ◽  
Z. Korade ◽  
E. Frank
Keyword(s):  
Spinal Cord ◽  
Dorsal Horn ◽  
Muscle Afferents ◽  
Cutaneous Afferents ◽  
In Ovo ◽  
Sensory Afferents ◽  
Chicken Embryos ◽  
Sensory Projections ◽  
Spinal Segments ◽  
Horn Development

Development of sensory projections was studied in cultured spinal segments with attached dorsal root ganglia. In spinal segments from stage 30 (E6.5) and older chicken embryos, prelabeled muscle and cutaneous afferents established appropriate projections. Cutaneous afferents terminated solely within the dorsolateral laminae, whereas some muscle afferents (presumably Ia afferents) projected ventrally towards motoneurons. Development of appropriate projections suggests that sufficient cues are preserved in spinal segments to support the formation of modality-specific sensory projections. Further, because these projections developed in the absence of muscle or skin, these results show that the continued presence of peripheral targets is not required for the formation of specific central projections after stage 29 (E6.0). Development of the dorsal horn in cultured spinal segments was assessed using the dorsal midline as a marker. In ovo, this midline structure appears at stage 29. Lack of midline formation in stage 28 and 29 cultured spinal segments suggests that the development of the dorsal horn is arrested in this preparation. This is consistent with earlier reports suggesting that dorsal horn development may be dependent on factors outside the spinal cord. Because dorsal horn development is blocked in cultured spinal segments, this preparation makes it possible to study the consequences of premature ingrowth of sensory axons into the spinal cord. In chicken embryos sensory afferents reach the spinal cord at stage 25 (E4.5) but do not arborize within the gray matter until stage 30. During this period dorsal horn cells are still being generated. In spinal segments, only those segments that have developed a midline at the time of culture support the formation of midline at the time of culture support the formation of specific sensory projections.(ABSTRACT TRUNCATED AT 250 WORDS)

scholarly journals In ovo feeding improves energy status of late-term chicken embryos

2005 ◽  
Vol 84 (5) ◽  
pp. 764-770 ◽  
Author(s):  
Z. Uni ◽  
P.R. Ferket ◽  
E. Tako ◽  
O. Kedar
Keyword(s):  
Energy Status ◽  
In Ovo ◽  
Chicken Embryos ◽  
In Ovo Feeding

Disruption of cytochrome P450 enzymes in the liver and small intestine in chicken embryos in ovo exposed to glyphosate

2020 ◽  
Vol 27 (14) ◽  
pp. 16865-16875 ◽  
Author(s):  
Mohamed Ahmed Fathi ◽  
Guofeng Han ◽  
Ruifen Kang ◽  
Dan Shen ◽  
Jiakun Shen ◽  
...  
Keyword(s):  
Cytochrome P450 ◽  
Small Intestine ◽  
Cytochrome P450 Enzymes ◽  
In Ovo ◽  
Chicken Embryos
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