No abstract available.
Betamethasone* ; Butyrates* ; Diethylpropion* ; Humans* ; Keratinocytes*

Halomonas can grow on diverse carbon sources. As it can be used for unsterile fermentation under high-salt conditions, it has been applied as a chassis for next-generation industrial biotechnology. Short-chain volatile fatty acids, including acetate, propionate, and butyrate, can be prepared from biomass and are expected to be novel carbon sources for microbial fermentation. Halomonas sp. TD01 and TD08 were subjected to shaking culture with 10-50 g/L butyrate, and they were found to effectively synthesize poly-3-hydroxybutyrate with butyrate as the carbon source. The highest yield of poly-3-hydroxybutyrate was achieved at butyrate concentration of 20 g/L (9.12 g/L and 7.37 g/L, respectively). Butyrate at the concentration > 20 g/L inhibited cell growth, and the yield of poly-3-hydroxybutyrate decreased to < 4 g/L when butyrate concentration was 50 g/L. Moreover, Halomonas sp. TD08 can accumulate the copolymer of 3-hydroxybutyrate and 3-hydroxyvalerate by using propionate and butyrate as carbon sources. However, propionate was toxic to cells. To be specific, when 2 g/L propionate and 20 g/L butyrate were simultaneously provided, cell dry weight and polymer titer were 0.83 g/L and 0.15 g/L, respectively. The addition of glycerol significantly improved cell growth and boosted the copolymer titer to 3.95 g/L, with 3-hydroxyvalerate monomer content of 8.76 mol%. Short-chain volatile fatty acids would be promising carbon sources for the production of polyhydroxyalkanoates by Halomonas.
Butyrates ; Carbon ; Fatty Acids, Volatile ; Halomonas ; Polyhydroxyalkanoates ; Propionates

Butyrate, normally produced by probiotics in the gut, not only provides energy for cells, but also changes the phosphorylation, acetylation and methylation levels of many proteins in cells. As a result, it affects the expression of many genes and the transmission of cell signals. Through G protein-coupled receptors, butyrate promotes the secretion of intestinal mucus and the formation of epithelial barriers, and attenuates the impacts of the pathogenic bacteria and their metabolites on human body. The Toll-like receptors (TLRs) are a group of pattern recognition receptors, and their activation causes the translocation of nuclear factor κB (NF-κB) from the cytoplasm to the nucleus and eventually leads to expression and secretion of various pro-inflammatory factors and chemokines. The expression of TLRs is also involved in the pathogenesis of some inflammatory diseases and tumors. The purpose of this review is to summarize the effects of butyrate on TLRs and their downstream signaling pathways. We not only summarized the production of butyrate, the expression of TLRs and the influence of their interaction on the body under the conditions of inflammation and tumor, but also discussed the potential role of butyrate as a bacterial metabolite in the treatments of some human diseases.
Humans ; Butyrates ; Toll-Like Receptors ; Acetylation ; Phosphorylation ; Inflammation

The egg is one of the most common food allergens, and immunologic reactivity to egg antigens may be an early marker of atopic disorders. Budesonide is a synthetic non-halogenated corticosteroid with 16 , 17 -butylidene dioxy portion, and it is one of the common causes of corticosteroid allergy together with tixocortol pivalate and hydrocortisone butyrate. The patient was a 12 year old female. She had developed atopic dermatitis mainly on the face since she was 1 year old. She applied budesonide cream for treating atopic dermatitis in our dermatologic clinic, but her facial lesion was aggravated. On past medical history, she had been suffered from an egg allergy since 1-year-old, and she was accidentally exposed to egg and developed large pruritic erythematous patch on entire body. This case could be considered as atopic dermatitis with egg and budesonide hypersensitivity on the basis of the clinical features and prick test, MAST, open food challenge and patch test.
Allergens ; Budesonide* ; Butyrates ; Child ; Dermatitis, Atopic* ; Egg Hypersensitivity ; Female ; Humans ; Hydrocortisone ; Hypersensitivity* ; Ovum* ; Patch Tests

The effect of DMSO and sodium butyrate on the production of recombinant hepatitis A virus (HAV) capsid protein VP1 was evaluated and optimized in the culture of stably transfected Drosophila melanogaster S2 cells using culture plates and spinner flasks. The effect of DMSO and sodium butyrate was also evaluated to improve the recombinant VP1 production in stably transfected Drosophila S2 cells. A production level of 0.88 mg of recombinant VP1/liter was obtained in the culture-plate culture of stably transfected S2 cells at 6 days after induction with 0.5 mM CuSO4. The supplements of 2% DMSO and 10 mM sodium butyrate at 4 days post-inoculation increased recombinant VP1 accumulation by 141 and 104%, respectively, resulting in 2.17 and 1.7 mg/liter of recombinant VP1 production. In spinner flasks, recombinant VP1 production reached maximum level at 9 days after induction with 0.5 mM CuSO4, with approximately 4.96 mg/liter of recombinant VP1 production level. When 2% DMSO or 10 mM sodium butyrate was added at 5 days post-inoculation, the recombinant VP1 production was increased to 8.35 and 5.85 mg/liter, respectively. However, the synergistic effects of DMSO and sodium butyrate were not observed. These results indicate that DMSO and/or sodium butyrate can be successfully used to improve the recombinant HAV VP1 production in culture plates and spinner flasks.
Butyrates ; Capsid Proteins ; Dimethyl Sulfoxide ; Drosophila ; Drosophila melanogaster ; Efficiency ; Hepatitis ; Hepatitis A ; Hepatitis A virus ; Sodium

OBJEVTIVETo synthesize phenoxybutyric acid derivatives as 5α-reductase inhibitors and test their biological activities in vitro.

METHODSEight analogues as nonsteroidal 5α-reductase inhibitors were designed and synthesized by substitution reaction of 6-(4-phenyl-piperazine-1-yl)-3(2H)-pyridazinone with phenoxybutyric acid derivatives.

RESULTS AND CONCLUSIONThe structures of the compounds were characterized by 1H-NMR and MS. Biological evaluation indicated that 7 out of the 8 compounds exhibited moderate 5α-reductase inhibitory activities, especially the compounds A1 and A7 with inhibition rates reaching 12.50% and 19.64% at the concentration of 3.3 × 10⁻⁵ mol/L, respectively.

5-alpha Reductase Inhibitors ; chemical synthesis ; pharmacology ; Butyrates ; chemistry ; pharmacology ; Drug Design

OBJECTIVETo explore the effect and mechanism of sodium butyrate on expression of human clotting factor VIII in vitro.

METHODSMouse NIH/3T3 cell line was transfected with recombinant plasmid vector pRC/RSV-BDD-hFVIII, which enclosed B-domain deleted (760aa approximately 1 639aa) human factor VIII cDNA (BDD-hFVIII cDNA). Then cells were incubated in Dulbecco's modification of Eagle's medium (DMEM) containing sodium butyrate for 24 hours, hFVIII: C and hFVIII: Ag in the cell culture medium were measured by ELISA assay and one-stage method, respectively. In addition, the effect of sodium butyrate on transcription of cDNA encoding the whole hFVIII, heavy and light chain of hFVIII was also investigated by means of run-on assay.

RESULTSAfter stimulation of sodium butyrate, the levels of hFVIII: C and hFVIII: Ag increased 70% than those of control. Run-on assay showed that sodium butyrate enhanced the transcription of cDNA which encoded heavy chain of hFVIII.

CONCLUSIONSodium butyrate can improve the expression of hFVIII through enhancing the transcription of hFVIII heavy chain encoding cDNA. It demonstrated that sodium butyrate had potential utility in inducing the expression of hFVIII in vitro.

3T3 Cells ; Animals ; Butyrates ; pharmacology ; Factor VIII ; genetics ; Gene Expression Regulation ; drug effects ; Humans ; Mice

During the routine impurity profile of lisinopril bulk drug by HPLC (high-performance liquid chromatography), a potential impurity was detected. Using multidimensional NMR (nuclear magnetic resonance) technique, the trace-level impurity was unambiguously identified to be 2-(-2-oxo-azocan-3-ylamino)-4-phenyl-butyric acid after isolation from lisinopril bulk drug by semi-preparative HPLC. Formation of the impurity was also discussed. To our knowledge, this is a novel impurity and not reported elsewhere.
Butyrates ; analysis ; isolation & purification ; Drug Contamination ; Lisinopril ; analysis ; Magnetic Resonance Spectroscopy ; Models, Molecular

Polyhydroxyalkanoates (PHAs) are a class of polyesters biosynthesized by microorganisms (esp. Ralstonia eutropha) under an unbalanced growth condition, and which are supposed to partly take the place of traditional plastics made from petroleum in the near future since they are harmless to the environment and biodegradable. Organic acids (mainly butyrate, lactate, propionate and acetate) produced from anaerobic digested food wastes, industrial wastes and sewage may be used as cheap carbon sources since the large amounts of the above wastes disposed by industry and family each year. In order to better understand the process of PHAs formation with acids as carbon sources, so as to increase the yields of PHAs. Biosynthesis of PHAs by R. eutropha during the dual nutrient-limitation-zone was investigated with mixed organic acids (the mass ratio of the four component acids was butyrate: propionate: acetate: lactate = 3: 3: 1: 1, which was simulated as once the result of anaerobic digestion of food wastes) as carbon sources and (NH4)2 SO4 as nitrogen source. Two different manners of maintaining the dual-nutrient-limitation zone were adopted by feeding mixed acids and (NH4 )2SO4 at determined rates to the fermentation culture which were free of carbon sources (manner A) or nitrogen sources (manner B) firstly. The results suggest that, first of all, the meaning of the limitation of mixed acids or (NH4)2 SO4 does not mean to limit the supply of them, but mean to feed as more as possible of carbon and nitrogen sources in order to meet the cell growth and PHAs formation of R. eutropha by the largest extent. However, it's indispensable to make the residual concentration of carbon and nitrogen sources as low as possible since organic acids are inhibitive to the cell growth, and most importantly, only under the presence of nitrogen during the PHAS formation period of the fermentation could R. eutropha produce more PHAs than any other unbalanced growth condition. Secondly, with the increase of the width of the dual-nutrient-limitation zone, the yield of PHAs would also increase, it suggest that most of the PHAs were biosynthesized during the dual-nutrient-limitation zone. Finally, in contrast with the dual-nutrient-limitation manner of limiting the nitrogen source at first (manner B), the dual-nutrient-limitation manner of limiting the carbon source at first (manner A) was more favorable for the production of PHAs, and the maximum production of PHAs of these two manners are 3.72 g/L and 2.55 g/L, respectively. It may be because that PHAs formation required enzymes could not be well developed when R. eutropha grow under the state of nitrogen limitation from the beginning of fermentation. Besides, yield of PHAs produced by the dual-nutrient-limitation fermentation is larger than that of the single-nutrient-limitation batch culture. Therefore, it seems that to increase the output of PHAs production, the strategy of maintaining as wide as possible the width of dual-nutrient (C, N)-limitation zone may be effective.
Acetates ; metabolism ; Butyrates ; metabolism ; Cupriavidus necator ; metabolism ; Fermentation ; physiology ; Lactates ; metabolism ; Polyhydroxyalkanoates ; biosynthesis ; Propionates ; metabolism

OBJECTIVETo explore the molecular mechanisms of apoptotic NB4 cells induced by the histone deacetylase inhibitor, sodium butyrate(SB).

METHODSSB was exposed to NB4 cells at a final concentration of 1.0 mmol/L. The untreated and treated cells were analysed with FACS and 2-dimensional electrophoresis (2-DE) at 0, 12, 24, 48 and 72 h. The changed protein spots were identified with MALDI-TOF-MS and ESI-TOF-MS/MS.

RESULTSSB induced apoptosis of NB4 cells. Twenty-one changed proteins involving apoptotic signal transduction, immunological regulation, transcriptional control, cellular metabolism, molecular transport and so on were identified. Thirteen of them had been reported to be related to apoptosis.

CONCLUSIONSB can induce apoptosis and many functional protein changes in tumor cells. These results pave the way to further explore the anti-tumor mechanism of SB.

Apoptosis ; drug effects ; genetics ; Butyrates ; pharmacology ; Cell Line, Tumor ; Flow Cytometry ; Humans ; Proteomics