Tissue-Specific Accumulation, Depuration, and Transformation of Triphenyl Phosphate (TPHP) in Adult Zebrafish (Danio rerio)

2016 ◽  
Vol 50 (24) ◽  
pp. 13555-13564 ◽  
Author(s):  
Guowei Wang ◽  
Zhongkun Du ◽  
Hanyan Chen ◽  
Yu Su ◽  
Shixiang Gao ◽  
...  
Keyword(s):  
Danio Rerio ◽  
Adult Zebrafish ◽  
Triphenyl Phosphate ◽  
Tissue Specific ◽  
Specific Accumulation

Tissue-Specific Accumulation, Elimination, and Toxicokinetics of Illicit Drugs in Adult Zebrafish (Danio rerio)

2021 ◽  
pp. 148153
Author(s):  
Xingxing Yin ◽  
Changsheng Guo ◽  
Yanghui Deng ◽  
Xiaowei Jin ◽  
Yanguo Teng ◽  
...  
Keyword(s):  
Danio Rerio ◽  
Illicit Drugs ◽  
Adult Zebrafish ◽  
Tissue Specific ◽  
Specific Accumulation

Sequence of fatty acid binding proteins and their tissue-specific expression in adult zebrafish (Danio rerio)

2000 ◽  
Vol 28 (5) ◽  
pp. A238-A238
Author(s):  
J. M. Wright ◽  
E. M. Denovan-Wright ◽  
M. Pierce ◽  
Y. Wang ◽  
M. K. Sharma ◽  
...  
Keyword(s):  
Fatty Acid ◽  
Danio Rerio ◽  
Binding Proteins ◽  
Fatty Acid Binding Proteins ◽  
Adult Zebrafish ◽  
Specific Expression ◽  
Fatty Acid Binding ◽  
Tissue Specific ◽  
Tissue Specific Expression

Axonal projections originating from raphe serotonergic neurons in the developing and adult zebrafish,Danio rerio, using transgenics to visualize raphe-specificpet1expression

2009 ◽  
Vol 512 (2) ◽  
pp. 158-182 ◽  
Author(s):  
Christina Lillesaar ◽  
Christian Stigloher ◽  
Birgit Tannhäuser ◽  
Mario F. Wullimann ◽  
Laure Bally-Cuif
Keyword(s):  
Danio Rerio ◽  
Adult Zebrafish ◽  
Serotonergic Neurons ◽  
Axonal Projections

scholarly journals Different action mechanisms of low- and high-level quercetin in the brains of adult zebrafish (Danio rerio)

2021 ◽  
Vol 223 ◽  
pp. 112597
Author(s):  
Xia Wu ◽  
Li-Jun Wang ◽  
Yu Hou ◽  
Rui-Ying Guo ◽  
Min Liu ◽  
...  
Keyword(s):  
Danio Rerio ◽  
Adult Zebrafish ◽  
Action Mechanisms ◽  
High Level

Tissue-specific accumulation of carotenoids in carrot roots

Planta ◽  
2006 ◽  
Vol 224 (5) ◽  
pp. 1028-1037 ◽  
Author(s):  
Malgorzata Baranska ◽  
Rafal Baranski ◽  
Hartwig Schulz ◽  
Thomas Nothnagel
Keyword(s):  
Tissue Specific ◽  
Specific Accumulation

scholarly journals Distribution of carnosine-like peptides in the nervous system of developing and adult zebrafish (Danio rerio) and embryonic effects of chronic carnosine exposure

2009 ◽  
Vol 337 (1) ◽  
pp. 45-61 ◽  
Author(s):  
Marie-Claude Senut ◽  
Seema Azher ◽  
Frank L. Margolis ◽  
Kamakshi Patel ◽  
Ahmad Mousa ◽  
...  
Keyword(s):  
Nervous System ◽  
Danio Rerio ◽  
Adult Zebrafish

scholarly journals Synaptic and epidermal accumulations of human acetylcholinesterase are encoded by alternative 3'-terminal exons.

1995 ◽  
Vol 15 (6) ◽  
pp. 2993-3002 ◽  
Author(s):  
S Seidman ◽  
M Sternfeld ◽  
R Ben Aziz-Aloya ◽  
R Timberg ◽  
D Kaufer-Nachum ◽  
...  
Keyword(s):  
Neuromuscular Junctions ◽  
Gene Transcript ◽  
Dna Encoding ◽  
Tissue Specific ◽  
Evolutionarily Conserved ◽  
Low Salt ◽  
Catalytically Active ◽  
Specific Accumulation ◽  
The Brain ◽  
Muscle Ache

Tissue-specific heterogeneity among mammalian acetylcholinesterases (AChE) has been associated with 3' alternative splicing of the primary AChE gene transcript. We have previously demonstrated that human AChE DNA encoding the brain and muscle AChE form and bearing the 3' exon E6 (ACHE-E6) induces accumulation of catalytically active AChE in myotomes and neuromuscular junctions (NMJs) of 2- and 3-day-old Xenopus embryos. Here, we explore the possibility that the 3'-terminal exons of two alternative human AChE cDNA constructs include evolutionarily conserved tissue-recognizable elements. To this end, DNAs encoding alternative human AChE mRNAs were microinjected into cleaving embryos of Xenopus laevis. In contrast to the myotomal expression demonstrated by ACHE-E6, DNA carrying intron 14 and alternative exon E5 (ACHE-I4/E5) promoted punctuated staining of epidermal cells and secretion of AChE into the external medium. Moreover, ACHE-E6-injected embryos displayed enhanced NMJ development, whereas ACHE-I4/E5-derived enzyme was conspicuously absent from muscles and NMJs and its expression in embryos had no apparent effect on NMJ development. In addition, cell-associated AChE from embryos injected with ACHE-I4/E5 DNA was biochemically distinct from that encoded by the muscle-expressible ACHE-E6, displaying higher electrophoretic mobility and greater solubility in low-salt buffer. These findings suggest that alternative 3'-terminal exons dictate tissue-specific accumulation and a particular biological role(s) of AChE, associate the 3' exon E6 with NMJ development, and indicate the existence of a putative secretory AChE form derived from the alternative I4/E5 AChE mRNA.

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