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Article ; Online: Observation on the ice crystal formation process of large yellow croaker (Pseudosciaena crocea) and the effect of multiple cryoprotectants pre-soaking treatments on frozen quality.

Yang, Zhikang / Ye, Guosen / Yang, Dazhang / Xie, Jing / Huo, Yilin

2023 Volume 113, Page(s) 104580

Abstract: By observing the formation behavior of ice crystals, the quality of food products under different freezing conditions can be intuitively judged. In this paper, large yellow croaker was taken as the research object, and a novel cryomicroscopic system was ... ...

Abstract	By observing the formation behavior of ice crystals, the quality of food products under different freezing conditions can be intuitively judged. In this paper, large yellow croaker was taken as the research object, and a novel cryomicroscopic system was developed to directly observe the structure of ice crystals during the freezing process. The cryoprotective effects of 4% sucrose +4% sorbitol (SU + SO), 4% xylo-oligosaccharide (XO), 4% xylo-oligosaccharide + 0.3% tetrasodium pyrophosphate (XO + TSPP) and 0.2% antifreeze protein (AFP) at different freezing temperatures were investigated. And the evaluation indicators, such as cell deformation degree, equivalent diameters, roundness, elongation and fractal dimension were introduced to quantify the damage of ice crystals to muscle tissues and fibers. The results indicate that reducing the freezing temperature and adding cryoprotectants can improve the quality of large yellow croaker. AFP has the best cryoprotective effect, with a reduction in cell deformation degree of 54.78% and 67.83% compared to the Control group at -5 °C and -20 °C, respectively. SU + SO and XO have the equivalent antifreeze effect, which is slightly inferior to XO + TSPP. In addition, physical parameters of large yellow croaker samples were measured to verify the influence of ice crystal structure on product quality. Therefore, direct observation of the ice crystal formation process and evaluation of ice crystal structure can accurately reflect the quality of frozen products, which is of great significance for the development of refrigeration and preservation technology.
MeSH term(s)	Animals ; Freezing ; Cryoprotective Agents/pharmacology ; Cryoprotective Agents/chemistry ; Ice ; alpha-Fetoproteins ; Cryopreservation/methods ; Perciformes ; Antifreeze Proteins/pharmacology ; Oligosaccharides/chemistry
Chemical Substances	Cryoprotective Agents ; Ice ; alpha-Fetoproteins ; Antifreeze Proteins ; Oligosaccharides
Language	English
Publishing date	2023-08-23
Publishing country	Netherlands
Document type	Journal Article
ZDB-ID	80098-3
ISSN	1090-2392 ; 0011-2240
ISSN (online)	1090-2392
ISSN	0011-2240
DOI	10.1016/j.cryobiol.2023.104580
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Article: Recent advances on air heating system of cabin for pure electric vehicles: A review.

Yang, Dazhang / Huo, Yilin / Zhang, Qing / Xie, Jing / Yang, Zhikang

Heliyon

2022 Volume 8, Issue 10, Page(s) e11032

Abstract: Due to the environmental protection and energy shortage, the electric vehicles (EV) is gradually replacing traditional fuel vehicles. EV generally use more energy for air conditioning system, especially EV have almost no waste heat from engine to be ... ...

Abstract	Due to the environmental protection and energy shortage, the electric vehicles (EV) is gradually replacing traditional fuel vehicles. EV generally use more energy for air conditioning system, especially EV have almost no waste heat from engine to be discharged to the passenger compartment to achieve thermal comfort in heating condition. The energy consumption of the heating system for EV will decrease the maximum mileage. Therefore, the energy saving technology for heating system is developing and applied for EV. The article introduced the advance of conventional and emerging heating system for the EV. The positive temperature coefficient (PTC) heater is a convenient heating method used in EV, but PTC heater has some defects such as low efficiency. The heat pump (HP) system is gradually replacing PTC. However, HP has various problems to be overcome, such as the heating capacity and efficiency in low temperature environment. In addition, other novel technologies are proposed to reduce the energy consumption. This article reviews the literature of novel heating methods for EV, introduces adsorption air conditioning systems (AAC), fuel combustion (FC), heat storage (HS), waste heat recovery (WHR), thermoelectric effect (TE) and magnetocaloric effect (ME). © 2017 Elsevier Inc. All rights reserved.
Language	English
Publishing date	2022-10-10
Publishing country	England
Document type	Journal Article ; Review
ZDB-ID	2835763-2
ISSN	2405-8440
ISSN	2405-8440
DOI	10.1016/j.heliyon.2022.e11032
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Article ; Online: Recent advances on air heating system of cabin for pure electric vehicles: A review

Yang, Dazhang / Huo, Yilin / Zhang, Qing / Xie, Jing / Yang, Zhikang

Heliyon. 2022 Oct., v. 8, no. 10 p.e11032-

2022

Abstract	Due to the environmental protection and energy shortage, the electric vehicles (EV) is gradually replacing traditional fuel vehicles. EV generally use more energy for air conditioning system, especially EV have almost no waste heat from engine to be discharged to the passenger compartment to achieve thermal comfort in heating condition. The energy consumption of the heating system for EV will decrease the maximum mileage. Therefore, the energy saving technology for heating system is developing and applied for EV. The article introduced the advance of conventional and emerging heating system for the EV. The positive temperature coefficient (PTC) heater is a convenient heating method used in EV, but PTC heater has some defects such as low efficiency. The heat pump (HP) system is gradually replacing PTC. However, HP has various problems to be overcome, such as the heating capacity and efficiency in low temperature environment. In addition, other novel technologies are proposed to reduce the energy consumption. This article reviews the literature of novel heating methods for EV, introduces adsorption air conditioning systems (AAC), fuel combustion (FC), heat storage (HS), waste heat recovery (WHR), thermoelectric effect (TE) and magnetocaloric effect (ME). © 2017 Elsevier Inc. All rights reserved.
Keywords	adsorption ; air ; energy ; environmental protection ; fuel combustion ; fuels ; heat pumps ; temperature ; waste heat recovery ; Electric vehicle ; Heating system ; Magnetocaloric ; Thermoelectric
Language	English
Dates of publication	2022-10
Publishing place	Elsevier Ltd
Document type	Article ; Online
Note	Use and reproduction
ZDB-ID	2835763-2
ISSN	2405-8440
ISSN	2405-8440
DOI	10.1016/j.heliyon.2022.e11032
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Article ; Online: Neuroprotective potential of phytochemicals isolated from Paeonia ostii ‘Feng Dan’ stamen

Peng, Xiao-Na / Zhou, Yang / Liu, Yan-Xiang / Huo, Yi-Lin / Ren, Jie-Yi / Bai, Zhang-Zhen / Zhang, Yan-Long / Tang, Jiang-Jiang

Industrial Crops & Products. 2023 Sept., v. 200 p.116808-

2023

Abstract: Paeonia ostii ‘Feng Dan’, traditionally known as an important medicinal and ornamental plant, is an emerging oilseed crop widely cultivated in China. As a byproduct, its stamens showed promising anti-neuroinflammation potential in our previous study. In ... ...

Abstract	Paeonia ostii ‘Feng Dan’, traditionally known as an important medicinal and ornamental plant, is an emerging oilseed crop widely cultivated in China. As a byproduct, its stamens showed promising anti-neuroinflammation potential in our previous study. In this work, an in-depth phytochemical investigation was firstly conducted through comprehensive spectra to elucidate the neuroprotective components. Two new compounds (+)-oxylactiflorin (1), (+)-3′′-methoxy-oxylactiflorin (2), and twenty-two known compounds were isolated and identified. In lipopolysaccharides-induced BV-2 cells, compound 2 exhibited excellent inhibitory property in inhibiting nitric oxide (NO) production with the lowest EC₅₀ value of 3.02 ± 1.60 µM among all tested compounds. Western blotting and molecular docking results demonstrated the feasible mechanism that 2 exerted anti-inflammatory activity mainly by binding with the key protein cyclooxygenase-2 (COX-2). Additionally, compound 2 showed potent protective effects on the oxidative damages of H₂O₂ or 6-Hydroxydopamine (6-OHDA)-treated PC12 cells. This work provides a theoretical basis of P. ostii stamens for developing into a promising functional tea or neuroprotective drug.
Keywords	Paeonia ostii ; anti-inflammatory activity ; byproducts ; drugs ; neuroprotective effect ; nitric oxide ; oilseed crops ; ornamental plants ; phytochemicals ; prostaglandin synthase ; tea ; China ; Paeonia ostii stamen ; Anti-neuroinflammation ; Cyclooxygenase-2 ; Neuroprotection
Language	English
Dates of publication	2023-09
Publishing place	Elsevier B.V.
Document type	Article ; Online
ZDB-ID	1132158-1
ISSN	1872-633X ; 0926-6690
ISSN (online)	1872-633X
ISSN	0926-6690
DOI	10.1016/j.indcrop.2023.116808
Database	NAL-Catalogue (AGRICOLA)

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Article ; Online: Differing effects of rapamycin and mTOR kinase inhibitors on protein synthesis.

Huo, Yilin / Iadevaia, Valentina / Proud, Christopher G

Biochemical Society transactions

2011 Volume 39, Issue 2, Page(s) 446–450

Abstract: mTOR (mammalian target of rapamycin) forms two distinct types of complex, mTORC (mTOR complex) 1 and 2. Rapamycin inhibits some of the functions of mTORC1, whereas newly developed mTOR kinase inhibitors interfere with the actions of both types of complex. ...

Abstract	mTOR (mammalian target of rapamycin) forms two distinct types of complex, mTORC (mTOR complex) 1 and 2. Rapamycin inhibits some of the functions of mTORC1, whereas newly developed mTOR kinase inhibitors interfere with the actions of both types of complex. We have explored the effects of rapamycin and mTOR kinase inhibitors on general protein synthesis and, using a new stable isotope-labelling method, the synthesis of specific proteins. In HeLa cells, rapamycin only had a modest effect on total protein synthesis, whereas mTOR kinase inhibitors decreased protein synthesis by approx. 30%. This does not seem to be due to the ability of mTOR kinase inhibitors to block the binding of eIFs (eukaryotic initiation factors) eIF4G and eIF4E. Analysis of the effects of the inhibitors on the synthesis of specific proteins showed a spectrum of behaviours. As expected, synthesis of proteins encoded by mRNAs that contain a 5'-TOP (5'-terminal oligopyrimidine tract) was impaired by rapamycin, but more strongly by mTOR kinase inhibition. Several proteins not known to be encoded by 5'-TOP mRNAs also showed similar behaviour. Synthesis of proteins encoded by 'non-TOP' mRNAs was less inhibited by mTOR kinase inhibitors and especially by rapamycin. The implications of our findings are discussed.
MeSH term(s)	Animals ; Humans ; Isotope Labeling/methods ; Models, Biological ; Protein Biosynthesis/drug effects ; Protein Biosynthesis/genetics ; Protein Kinase Inhibitors/pharmacology ; Sirolimus/pharmacology ; TOR Serine-Threonine Kinases/antagonists & inhibitors
Chemical Substances	Protein Kinase Inhibitors ; MTOR protein, human (EC 2.7.1.1) ; TOR Serine-Threonine Kinases (EC 2.7.1.1) ; Sirolimus (W36ZG6FT64)
Language	English
Publishing date	2011-04
Publishing country	England
Document type	Journal Article ; Research Support, Non-U.S. Gov't ; Review
ZDB-ID	184237-7
ISSN	1470-8752 ; 0300-5127
ISSN (online)	1470-8752
ISSN	0300-5127
DOI	10.1042/BST0390446
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Article ; Online: Roles of the mammalian target of rapamycin, mTOR, in controlling ribosome biogenesis and protein synthesis.

Iadevaia, Valentina / Huo, Yilin / Zhang, Ze / Foster, Leonard J / Proud, Christopher G

Biochemical Society transactions

2012 Volume 40, Issue 1, Page(s) 168–172

Abstract: mTORC1 (mammalian target of rapamycin complex 1) is controlled by diverse signals (e.g. hormones, growth factors, nutrients and cellular energy status) and regulates a range of processes including anabolic metabolism, cell growth and cell division. We ... ...

Abstract	mTORC1 (mammalian target of rapamycin complex 1) is controlled by diverse signals (e.g. hormones, growth factors, nutrients and cellular energy status) and regulates a range of processes including anabolic metabolism, cell growth and cell division. We have studied the impact of inhibiting mTOR on protein synthesis in human cells. Partial inhibition of mTORC1 by rapamycin has only a limited impact on protein synthesis, but inhibiting mTOR kinase activity causes much greater inhibition of protein synthesis. Using a pulsed stable-isotope-labelling technique, we show that the rapamycin and mTOR (mammalian target of rapamycin) kinase inhibitors have differential effects on the synthesis of specific proteins. In particular, the synthesis of proteins encoded by mRNAs that have a 5'-terminal pyrimidine tract is strongly inhibited by mTOR kinase inhibitors. Many of these mRNAs encode ribosomal proteins. mTORC1 also promotes the synthesis of rRNA, although the mechanisms involved remain to be clarified. We found that mTORC1 also regulates the processing of the precursors of rRNA. mTORC1 thus co-ordinates several steps in ribosome biogenesis.
MeSH term(s)	Animals ; Gene Expression Regulation, Enzymologic ; Humans ; Mechanistic Target of Rapamycin Complex 1 ; Multiprotein Complexes ; Protein Biosynthesis/drug effects ; Proteins/metabolism ; Ribosomes/genetics ; Ribosomes/metabolism ; Sirolimus/pharmacology ; TOR Serine-Threonine Kinases/antagonists & inhibitors ; TOR Serine-Threonine Kinases/metabolism ; TOR Serine-Threonine Kinases/physiology ; Transcription Factors/metabolism
Chemical Substances	CRTC2 protein, human ; Multiprotein Complexes ; Proteins ; Transcription Factors ; Mechanistic Target of Rapamycin Complex 1 (EC 2.7.11.1) ; TOR Serine-Threonine Kinases (EC 2.7.11.1) ; Sirolimus (W36ZG6FT64)
Language	English
Publishing date	2012-01-19
Publishing country	England
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	184237-7
ISSN	1470-8752 ; 0300-5127
ISSN (online)	1470-8752
ISSN	0300-5127
DOI	10.1042/BST20110682
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Article ; Online: 5'-AMP-activated protein kinase-activating transcription factor 1 cascade modulates human monocyte-derived macrophages to atheroprotective functions in response to heme or metformin.

Wan, Xinyi / Huo, Yilin / Johns, Michael / Piper, Emma / Mason, Justin C / Carling, David / Haskard, Dorian O / Boyle, Joseph J

Arteriosclerosis, thrombosis, and vascular biology

2013 Volume 33, Issue 11, Page(s) 2470–2480

Abstract: Objective: Intraplaque hemorrhage (IPH) is an important driver of the progression of atherosclerotic plaques. Recently, we characterized Mhem as a novel macrophage phenotype that limits the atherogenicity of IPH. Mhem are directed by activating ... ...

Abstract	Objective: Intraplaque hemorrhage (IPH) is an important driver of the progression of atherosclerotic plaques. Recently, we characterized Mhem as a novel macrophage phenotype that limits the atherogenicity of IPH. Mhem are directed by activating transcription factor 1 (ATF1), which is activated by phosphorylation. A better understanding of the counteratherogenic ATF1-Mhem pathway may facilitate antiatherosclerotic therapies. Approach and results: We tested the hypothesis that heme in pathologically relevant concentrations activates the ATF1-Mhem pathway via 5'-AMP-activated protein kinase (AMPK) in primary human monocyte-derived macrophages and mouse bone marrow macrophages. We found that heme (10 μmol/L) activates AMPK, and downstream ATF1-mediated coinduction of heme oxygenase and liver X receptor that characterize Mhem. Heme increased macrophage phospho-AMPK, phospho-ATF1, and its target genes, and these effects were inhibited by the AMPK antagonist dorsomorphin, or by AMPK-knockdown with small inhibitory ribonucleic acid. The AMPK-activating oral hypoglycemic agent metformin also induced and phosphorylated ATF1 at a clinically relevant concentration (10 μmol/L). Functional effects of heme and metformin were inhibited by AMPK-knockdown and included suppression of macrophage oxidative stress; increased cholesterol export; protection from foam-cell formation; and suppression of macrophage inflammatory activation (human leukocyte antigen type DR expression). Conclusions: Our data indicate that heme activates the ATF1 pathway in human macrophages via AMPK, and that a similar response occurs after treatment of cells with metformin. Our results suggest an in vitro mechanism that may explain the clinical evidence that metformin has vascular protective effects beyond its role in treating hyperglycemia.
MeSH term(s)	AMP-Activated Protein Kinases/genetics ; AMP-Activated Protein Kinases/metabolism ; Activating Transcription Factor 1/genetics ; Activating Transcription Factor 1/metabolism ; Atherosclerosis/metabolism ; Heme/pharmacology ; Heme Oxygenase-1/genetics ; Heme Oxygenase-1/metabolism ; Humans ; Hypoglycemic Agents/pharmacology ; Liver X Receptors ; Macrophages/cytology ; Macrophages/drug effects ; Macrophages/metabolism ; Metformin/pharmacology ; Orphan Nuclear Receptors/genetics ; Orphan Nuclear Receptors/metabolism ; Oxidative Stress/drug effects ; Oxidative Stress/physiology ; Primary Cell Culture ; RNA, Small Interfering/pharmacology ; Signal Transduction/drug effects ; Signal Transduction/physiology
Chemical Substances	ATF1 protein, human ; Activating Transcription Factor 1 ; Hypoglycemic Agents ; Liver X Receptors ; Orphan Nuclear Receptors ; RNA, Small Interfering ; Heme (42VZT0U6YR) ; Metformin (9100L32L2N) ; Heme Oxygenase-1 (EC 1.14.14.18) ; AMP-Activated Protein Kinases (EC 2.7.11.31)
Language	English
Publishing date	2013-09-19
Publishing country	United States
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	1221433-4
ISSN	1524-4636 ; 1079-5642
ISSN (online)	1524-4636
ISSN	1079-5642
DOI	10.1161/ATVBAHA.113.300986
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Article ; Online: Stable isotope-labelling analysis of the impact of inhibition of the mammalian target of rapamycin on protein synthesis.

Huo, Yilin / Iadevaia, Valentina / Yao, Zhong / Kelly, Isabelle / Cosulich, Sabina / Guichard, Sylvie / Foster, Leonard J / Proud, Christopher G

The Biochemical journal

2012 Volume 444, Issue 1, Page(s) 141–151

Abstract: mTORC1 [mTOR (mammalian target of rapamycin) complex 1] regulates diverse cell functions. mTORC1 controls the phosphorylation of several proteins involved in mRNA translation and the translation of specific mRNAs, including those containing a 5'-TOP (5'- ... ...

Abstract	mTORC1 [mTOR (mammalian target of rapamycin) complex 1] regulates diverse cell functions. mTORC1 controls the phosphorylation of several proteins involved in mRNA translation and the translation of specific mRNAs, including those containing a 5'-TOP (5'-terminal oligopyrimidine). To date, most of the proteins encoded by known 5'-TOP mRNAs are proteins involved in mRNA translation, such as ribosomal proteins and elongation factors. Rapamycin inhibits some mTORC1 functions, whereas mTOR-KIs (mTOR kinase inhibitors) interfere with all of them. mTOR-KIs inhibit overall protein synthesis more strongly than rapamycin. To study the effects of rapamycin or mTOR-KIs on synthesis of specific proteins, we applied pSILAC [pulsed SILAC (stable isotope-labelling with amino acids in cell culture)]. Our results reveal, first, that mTOR-KIs and rapamycin differentially affect the synthesis of many proteins. Secondly, mTOR-KIs inhibit the synthesis of proteins encoded by 5'-TOP mRNAs much more strongly than rapamycin does, revealing that these mRNAs are controlled by rapamycin-insensitive outputs from mTOR. Thirdly, the synthesis of certain other proteins shows a similar pattern of inhibition. Some of them appear to be encoded by 'novel' 5'-TOP mRNAs; they include proteins which, like known 5'-TOP mRNA-encoded proteins, are involved in protein synthesis, whereas others are enzymes involved in intermediary or anabolic metabolism. These results indicate that mTOR signalling may promote diverse biosynthetic processes through the translational up-regulation of specific mRNAs. Lastly, a SILAC-based approach revealed that, although rapamycin and mTOR-KIs have little effect on general protein stability, they stabilize proteins encoded by 5'-TOP mRNAs.
MeSH term(s)	Carbon Isotopes ; Eukaryotic Initiation Factor-4E/metabolism ; HeLa Cells ; Humans ; Indoles/pharmacology ; Isotope Labeling ; Morpholines/pharmacology ; Nitrogen Isotopes ; Protein Biosynthesis/drug effects ; Protein Biosynthesis/genetics ; Purines/pharmacology ; RNA, Messenger/metabolism ; Ribosomes/metabolism ; Sirolimus/pharmacology ; TOR Serine-Threonine Kinases/antagonists & inhibitors
Chemical Substances	Carbon Isotopes ; Eukaryotic Initiation Factor-4E ; Indoles ; Morpholines ; Nitrogen Isotopes ; Purines ; RNA, Messenger ; (5-(2,4-bis((3S)-3-methylmorpholin-4-yl)pyrido(2,3-d)pyrimidin-7-yl)-2-methoxyphenyl)methanol (970JJ37FPW) ; TOR Serine-Threonine Kinases (EC 2.7.1.1) ; PP242 (H5669VNZ7V) ; Sirolimus (W36ZG6FT64)
Language	English
Publishing date	2012-03-13
Publishing country	England
Document type	Journal Article ; Research Support, Non-U.S. Gov't
ZDB-ID	2969-5
ISSN	1470-8728 ; 0006-2936 ; 0306-3275 ; 0264-6021
ISSN (online)	1470-8728
ISSN	0006-2936 ; 0306-3275 ; 0264-6021
DOI	10.1042/BJ20112107
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