2003
DOI: 10.1271/bbb.67.736
|View full text |Cite
|
Sign up to set email alerts
|

Dietary Protein as a Potent Regulator of the Hyaluronan Synthase Gene in Rat Skin

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

2
15
0

Year Published

2007
2007
2020
2020

Publication Types

Select...
8
1

Relationship

5
4

Authors

Journals

citations
Cited by 19 publications
(17 citation statements)
references
References 42 publications
2
15
0
Order By: Relevance
“…Each essential AA deficiency resulted in a pronounced decrease in hyaluron production in WS1 cells. In our previous study, we revealed that the expression of the HAS2 gene was highly sensitive to the quantity and quality of the dietary protein (Oishi et al, 2003). Taken together, our results suggest that such dietary patterns may lead to skin dysfunction and various cutaneous diseases.…”
Section: Discussionsupporting
confidence: 57%
See 1 more Smart Citation
“…Each essential AA deficiency resulted in a pronounced decrease in hyaluron production in WS1 cells. In our previous study, we revealed that the expression of the HAS2 gene was highly sensitive to the quantity and quality of the dietary protein (Oishi et al, 2003). Taken together, our results suggest that such dietary patterns may lead to skin dysfunction and various cutaneous diseases.…”
Section: Discussionsupporting
confidence: 57%
“…We previously demonstrated that hyaluronan synthesis was down-regulated by a low quality of dietary protein, such as gluten (Oishi et al, 2003). The quality of dietary protein can be estimated AAs and Gln is a key factor for the enhancement of skin collagen synthesis in protein-malnourished rats.…”
Section: Introductionmentioning
confidence: 99%
“…Real-time PCR reactions were conducted using the ABI Prism 7000 Sequence Detection System (Applied Biosystems Japan Ltd., Tokyo, Japan) with TaqMan ® Universal PCR Master Mix (Applied Biosystems Japan). The primers and probes of β-actin (used as an internal control) were synthesized according to the method described by Oishi et al (2003). The primers and probes of UCP1 and Adrb3 were TaqMan ® Gene Expression Assays (Applied Biosystems Japan).…”
Section: Quantitative Real-time Polymerase Chain Reaction (Pcr) Totalmentioning
confidence: 99%
“…Extraction of total RNA and synthesis of complementary DNA were performed as described previously. 12) Quantitative PCR primers and hybridization probes were synthesized by Applied Biosystems (Foster, IN). The oligonucleotide primers of IGFBP-1 were designed to amplify nucleo- A time course analysis indicated that the production of IGFBP-1 was increased significantly in HepG2 cells exposed to a 3 mM Cd 2þ for 72 and 144 h (data not shown).…”
Section: )mentioning
confidence: 99%