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  1. Article ; Online: Cloning, expression profiling, and effects of fasting status on neuropeptide Y in Schizothorax davidi.

    Deng, Xingxing / Lei, Luo / Yuan, Dengyue / Zheng, Zonglin / Zhu, Chengke / Luo, Hui / Ye, Hua / Li, Dongmei / Wang, Jian / Li, Baohai / Lv, Guangjun / Zhou, Chaowei

    Journal of food biochemistry

    2019  Volume 43, Issue 7, Page(s) e12892

    Abstract: ... in China. How to strengthen the production performance of S. davidi is a hot research area. Neuropeptide Y ... To better comprehend the mechanism that neuropeptide Y (npy) regulates feeding in Schizothorax ... davidi, we cloned and identified the full-length cDNA sequence of the npy gene in this species using RACE ...

    Abstract To better comprehend the mechanism that neuropeptide Y (npy) regulates feeding in Schizothorax davidi, we cloned and identified the full-length cDNA sequence of the npy gene in this species using RACE technology. Subsequently, we explored the npy mRNA distribution in 18 tissues and investigated the expression of npy mRNA at postprandial and fasting stages. We found that the npy full-length cDNA sequence is 803 bp. Moreover, npy mRNAs extensively expressed in all detected tissues, with the highest expression in hypothalamus. In postprandial study, the expression of npy mRNA in the hypothalamus was significantly decreased after eating (p < 0.01). In addition, the expression of the npy gene was significantly increased on the fifth day after fasting (p < 0.05). However, after refeeding, the expression of the npy gene was decreased significantly on days 9, 11, and 14 (p < 0.01). Our research suggest that npy may have an orexigenic role in S. davidi. PRACTICAL APPLICATIONS: S. davidi, a coldwater fish native to China, has high economic value, and it has gained great popularity. To date, there is still no large-scale breeding of S. davidi in China. How to strengthen the production performance of S. davidi is a hot research area. Neuropeptide Y (NPY), a 36-amino-acid single-chain polypeptide, is one of the main appetite regulation factors. However, to date, no studies have reported on the biological function of npy in the feeding of S. davidi. In our study, we revealed that the trend of hypothalamic npy expression during the postprandial and fasting stages. The results suggested that npy might be an appetite-promoting factor in this species. Overall, we provide the theoretical basis for how to strengthen the production performance of S. davidi through appetite regulation.
    MeSH term(s) Animals ; Appetite Regulation/physiology ; China ; Cloning, Molecular ; Cyprinidae/genetics ; Cyprinidae/physiology ; Fasting/psychology ; Fish Proteins/genetics ; Fish Proteins/metabolism ; Gene Expression Profiling ; Hypothalamus/physiology ; Male ; Neuropeptide Y/genetics ; Neuropeptide Y/metabolism ; Postprandial Period/physiology ; RNA, Messenger/genetics
    Chemical Substances Fish Proteins ; Neuropeptide Y ; RNA, Messenger
    Language English
    Publishing date 2019-05-08
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 433846-7
    ISSN 1745-4514 ; 0145-8884
    ISSN (online) 1745-4514
    ISSN 0145-8884
    DOI 10.1111/jfbc.12892
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  2. Article: Cloning, expression profiling, and effects of fasting status on neuropeptide Y in Schizothorax davidi

    Deng, Xingxing / Lei, Luo / Li, Baohai / Li, Dongmei / Luo, Hui / Lv, Guangjun / Wang, Jian / Ye, Hua / Yuan, Dengyue / Zheng, Zonglin / Zhou, Chaowei / Zhu, Chengke

    Journal of food biochemistry. 2019 July, v. 43, no. 7

    2019  

    Abstract: ... in China. How to strengthen the production performance of S. davidi is a hot research area. Neuropeptide Y ... To better comprehend the mechanism that neuropeptide Y (npy) regulates feeding in Schizothorax ... davidi, we cloned and identified the full‐length cDNA sequence of the npy gene in this species using RACE ...

    Abstract To better comprehend the mechanism that neuropeptide Y (npy) regulates feeding in Schizothorax davidi, we cloned and identified the full‐length cDNA sequence of the npy gene in this species using RACE technology. Subsequently, we explored the npy mRNA distribution in 18 tissues and investigated the expression of npy mRNA at postprandial and fasting stages. We found that the npy full‐length cDNA sequence is 803 bp. Moreover, npy mRNAs extensively expressed in all detected tissues, with the highest expression in hypothalamus. In postprandial study, the expression of npy mRNA in the hypothalamus was significantly decreased after eating (p < 0.01). In addition, the expression of the npy gene was significantly increased on the fifth day after fasting (p < 0.05). However, after refeeding, the expression of the npy gene was decreased significantly on days 9, 11, and 14 (p < 0.01). Our research suggest that npy may have an orexigenic role in S. davidi. PRACTICAL APPLICATIONS: S. davidi, a coldwater fish native to China, has high economic value, and it has gained great popularity. To date, there is still no large‐scale breeding of S. davidi in China. How to strengthen the production performance of S. davidi is a hot research area. Neuropeptide Y (NPY), a 36‐amino‐acid single‐chain polypeptide, is one of the main appetite regulation factors. However, to date, no studies have reported on the biological function of npy in the feeding of S. davidi. In our study, we revealed that the trend of hypothalamic npy expression during the postprandial and fasting stages. The results suggested that npy might be an appetite‐promoting factor in this species. Overall, we provide the theoretical basis for how to strengthen the production performance of S. davidi through appetite regulation.
    Keywords amino acids ; appetite ; breeding ; cold-water fish ; complementary DNA ; economic valuation ; fasting ; food intake ; genes ; hypothalamus ; messenger RNA ; neuropeptide Y ; nucleotide sequences ; polypeptides ; refeeding ; Schizothorax ; tissues ; China
    Language English
    Dates of publication 2019-07
    Publishing place John Wiley & Sons, Ltd
    Document type Article
    Note JOURNAL ARTICLE
    ZDB-ID 433846-7
    ISSN 1745-4514 ; 0145-8884
    ISSN (online) 1745-4514
    ISSN 0145-8884
    DOI 10.1111/jfbc.12892
    Database NAL-Catalogue (AGRICOLA)

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  3. Book ; Online: Advances in Mechanisms of Renal Fibrosis

    Lan, Hui Y. / Nikolic-Paterson, David J.

    2018  

    Abstract: Scarring of the glomerular and tubulointerstitial compartments is a hallmark of progressive kidney disease. Renal fibrosis involves a complex interplay between kidney cells, leukocytes and fibroblasts in which transforming growth factor-β (TGF-β) plays a ...

    Abstract Scarring of the glomerular and tubulointerstitial compartments is a hallmark of progressive kidney disease. Renal fibrosis involves a complex interplay between kidney cells, leukocytes and fibroblasts in which transforming growth factor-β (TGF-β) plays a key role. This eBook provides a comprehensive update on TGF-β signalling pathways and introduces a range of cellular and molecular mechanisms involved in renal fibrosis both upstream and downstream of TGF-β. The wide variety of potential new targets described herein bodes well for the future development of effective therapies to tackle the major clinical problem of progressive renal fibrosis
    Keywords Science (General) ; Physiology
    Size 1 electronic resource (84 p.)
    Publisher Frontiers Media SA
    Document type Book ; Online
    Note English ; Open Access
    HBZ-ID HT020101814
    ISBN 9782889454990 ; 2889454991
    Database ZB MED Catalogue: Medicine, Health, Nutrition, Environment, Agriculture

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  4. Article ; Online: Group 1B phospholipase A

    Hui, David Y

    Biochimica et biophysica acta. Molecular and cell biology of lipids

    2018  Volume 1864, Issue 6, Page(s) 784–788

    Abstract: The group 1B phospholipase ... ...

    Abstract The group 1B phospholipase A
    MeSH term(s) Animals ; Humans ; Lipids/physiology ; Lung/metabolism ; Metabolic Diseases/metabolism ; Phospholipases A2/metabolism ; Pneumonia/metabolism
    Chemical Substances Lipids ; Phospholipases A2 (EC 3.1.1.4)
    Language English
    Publishing date 2018-07-09
    Publishing country Netherlands
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 60-7
    ISSN 1879-2618 ; 1879-2596 ; 1879-260X ; 1872-8006 ; 1879-2642 ; 1879-2650 ; 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    ISSN (online) 1879-2618 ; 1879-2596 ; 1879-260X ; 1872-8006 ; 1879-2642 ; 1879-2650
    ISSN 0006-3002 ; 0005-2728 ; 0005-2736 ; 0304-4165 ; 0167-4838 ; 1388-1981 ; 0167-4889 ; 0167-4781 ; 0304-419X ; 1570-9639 ; 0925-4439 ; 1874-9399
    DOI 10.1016/j.bbalip.2018.07.001
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  5. Article ; Online: Inactivation of Group 1B Phospholipase A

    Haller, April M / Wolfkiel, Patrick R / Jaeschke, Anja / Hui, David Y

    International journal of molecular sciences

    2023  Volume 24, Issue 22

    Abstract: Phospholipase ... ...

    Abstract Phospholipase A
    MeSH term(s) Mice ; Animals ; Group IB Phospholipases A2/metabolism ; Mice, Inbred C57BL ; Colitis/chemically induced ; Colitis/genetics ; Colitis/metabolism ; Colon/pathology ; Colitis, Ulcerative/metabolism ; Phospholipases A2/genetics ; Phospholipases A2/metabolism ; Cytokines/metabolism ; Dextran Sulfate/toxicity ; Disease Models, Animal ; Intestinal Mucosa/metabolism
    Chemical Substances Group IB Phospholipases A2 (EC 3.1.1.4) ; Phospholipases A2 (EC 3.1.1.4) ; Cytokines ; Dextran Sulfate (9042-14-2)
    Language English
    Publishing date 2023-11-10
    Publishing country Switzerland
    Document type Journal Article
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms242216155
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  6. Article ; Online: The good side of cholesterol: a requirement for maintenance of intestinal integrity.

    Hui, David Y

    Journal of lipid research

    2017  Volume 58, Issue 10, Page(s) 1935–1936

    MeSH term(s) Animals ; Cholesterol ; Ezetimibe ; Intestines ; Mice
    Chemical Substances Cholesterol (97C5T2UQ7J) ; Ezetimibe (EOR26LQQ24)
    Language English
    Publishing date 2017-08-02
    Publishing country United States
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Comment
    ZDB-ID 80154-9
    ISSN 1539-7262 ; 0022-2275
    ISSN (online) 1539-7262
    ISSN 0022-2275
    DOI 10.1194/jlr.C079715
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: LDL receptor-related protein 1 and its interacting partners in tissue homeostasis.

    Jaeschke, Anja / Hui, David Y

    Current opinion in lipidology

    2021  Volume 32, Issue 5, Page(s) 301–307

    Abstract: Purpose of review: LDL receptor-related protein 1 (LRP1) is a multifunctional protein with endocytic and signal transduction properties due to its interaction with numerous extracellular ligands and intracellular proteins. This brief review highlights ... ...

    Abstract Purpose of review: LDL receptor-related protein 1 (LRP1) is a multifunctional protein with endocytic and signal transduction properties due to its interaction with numerous extracellular ligands and intracellular proteins. This brief review highlights key developments in identifying novel functions of LRP1 in liver, lung, and the central nervous system in disease pathogenesis.
    Recent findings: In hepatocytes, LRP1 complexes with phosphatidylinositol 4-phosphate 5-kinase-1 and its related protein to maintain intracellular levels of phosphatidylinositol (4,5) bisphosphate and preserve lysosome and mitochondria integrity. In contrast, in smooth muscle cells, macrophages, and endothelial cells, LRP1 interacts with various different extracellular ligands and intracellular proteins in a tissue-dependent and microenvironment-dependent manner to either enhance or suppress inflammation, disease progression or resolution. Similarly, LRP1 expression in astrocytes and oligodendrocyte progenitor cells regulates cell differentiation and maturation in a developmental-dependent manner to modulate neurogenesis, gliogenesis, and white matter repair after injury.
    Summary: LRP1 modulates metabolic disease manifestation, inflammation, and differentiation in a cell-dependent, time-dependent, and tissue-dependent manner. Whether LRP1 expression is protective or pathogenic is dependent on its interaction with specific ligands and intracellular proteins, which in turn is dependent on the cell type and the microenvironment where these cells reside.
    MeSH term(s) Endothelial Cells/metabolism ; Homeostasis ; Humans ; Low Density Lipoprotein Receptor-Related Protein-1/genetics ; Low Density Lipoprotein Receptor-Related Protein-1/metabolism ; Macrophages/metabolism ; Myocytes, Smooth Muscle/metabolism ; Receptors, LDL/metabolism
    Chemical Substances Low Density Lipoprotein Receptor-Related Protein-1 ; Receptors, LDL
    Language English
    Publishing date 2021-11-23
    Publishing country England
    Document type Journal Article ; Research Support, N.I.H., Extramural ; Review
    ZDB-ID 1045394-5
    ISSN 1473-6535 ; 0957-9672
    ISSN (online) 1473-6535
    ISSN 0957-9672
    DOI 10.1097/MOL.0000000000000776
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  8. Article ; Online: Apolipoprotein E in Cardiometabolic and Neurological Health and Diseases.

    Alagarsamy, Jeyashree / Jaeschke, Anja / Hui, David Y

    International journal of molecular sciences

    2022  Volume 23, Issue 17

    Abstract: A preponderance of evidence obtained from genetically modified mice and human population studies reveals the association of apolipoprotein E (apoE) deficiency and polymorphisms with pathogenesis of numerous chronic diseases, including atherosclerosis, ... ...

    Abstract A preponderance of evidence obtained from genetically modified mice and human population studies reveals the association of apolipoprotein E (apoE) deficiency and polymorphisms with pathogenesis of numerous chronic diseases, including atherosclerosis, obesity/diabetes, and Alzheimer's disease. The human
    MeSH term(s) Animals ; Apolipoprotein E2/metabolism ; Apolipoprotein E3/genetics ; Apolipoprotein E4/genetics ; Apolipoproteins E/genetics ; Apolipoproteins E/metabolism ; Atherosclerosis/genetics ; Cardiovascular Diseases/metabolism ; Humans ; Mice ; Receptors, LDL/genetics
    Chemical Substances ApoE protein, human ; Apolipoprotein E2 ; Apolipoprotein E3 ; Apolipoprotein E4 ; Apolipoproteins E ; Receptors, LDL
    Language English
    Publishing date 2022-08-31
    Publishing country Switzerland
    Document type Journal Article ; Review
    ZDB-ID 2019364-6
    ISSN 1422-0067 ; 1422-0067 ; 1661-6596
    ISSN (online) 1422-0067
    ISSN 1422-0067 ; 1661-6596
    DOI 10.3390/ijms23179892
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  9. Article ; Online: Apolipoprotein E in Cardiometabolic and Neurological Health and Diseases

    Jeyashree Alagarsamy / Anja Jaeschke / David Y. Hui

    International Journal of Molecular Sciences, Vol 23, Iss 9892, p

    2022  Volume 9892

    Abstract: A preponderance of evidence obtained from genetically modified mice and human population studies reveals the association of apolipoprotein E (apoE) deficiency and polymorphisms with pathogenesis of numerous chronic diseases, including atherosclerosis, ... ...

    Abstract A preponderance of evidence obtained from genetically modified mice and human population studies reveals the association of apolipoprotein E (apoE) deficiency and polymorphisms with pathogenesis of numerous chronic diseases, including atherosclerosis, obesity/diabetes, and Alzheimer’s disease. The human APOE gene is polymorphic with three major alleles, ε2, ε3 and ε4, encoding apoE2, apoE3, and apoE4, respectively. The APOE gene is expressed in many cell types, including hepatocytes, adipocytes, immune cells of the myeloid lineage, vascular smooth muscle cells, and in the brain. ApoE is present in subclasses of plasma lipoproteins, and it mediates the clearance of atherogenic lipoproteins from plasma circulation via its interaction with LDL receptor family proteins and heparan sulfate proteoglycans. Extracellular apoE also interacts with cell surface receptors and confers signaling events for cell regulation, while apoE expressed endogenously in various cell types regulates cell functions via autocrine and paracrine mechanisms. This review article focuses on lipoprotein transport-dependent and -independent mechanisms by which apoE deficiency or polymorphisms contribute to cardiovascular disease, metabolic disease, and neurological disorders.
    Keywords apolipoprotein E (apoE) ; lipoprotein receptors ; atherosclerosis ; inflammatory response ; Alzheimer’s disease ; signal transduction ; Biology (General) ; QH301-705.5 ; Chemistry ; QD1-999
    Language English
    Publishing date 2022-08-01T00:00:00Z
    Publisher MDPI AG
    Document type Article ; Online
    Database BASE - Bielefeld Academic Search Engine (life sciences selection)

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  10. Article: Group 1B phospholipase A2 in metabolic and inflammatory disease modulation

    Hui, David Y

    Biochimica et biophysica acta. 2019 June, v. 1864, no. 6

    2019  

    Abstract: The group 1B phospholipase A2 (PLA2G1B) is a secreted phospholipase that catalyzes the hydrolytic removal of the sn-2 fatty acyl moiety from phospholipids. This enzyme is synthesized most abundantly in the pancreas and is also expressed in the lung. The ... ...

    Abstract The group 1B phospholipase A2 (PLA2G1B) is a secreted phospholipase that catalyzes the hydrolytic removal of the sn-2 fatty acyl moiety from phospholipids. This enzyme is synthesized most abundantly in the pancreas and is also expressed in the lung. The first part of this review article focuses on the role of pancreatic-derived PLA2G1B in mediating lipid absorption and discusses how the PLA2G1B-derived metabolic product contributes to cardiometabolic diseases, including obesity, hyperinsulinemia, hyperlipidemia, and atherosclerosis. The anti-helminth properties of PLA2G1B will also be discussed. The second part of this review will focus on PLA2G1B expressed in the lung, and in vitro data suggest that how this enzyme may modulate lung inflammation via both hydrolytic activity-dependent and -dependent mechanisms. Finally, recent studies revealing a relationship between PLA2G1B and cancer will also be discussed. This article is part of a Special Issue entitled Novel functions of phospholipase A2 Guest Editors: Makoto Murakami and Gerard Lambeau.
    Keywords absorption ; atherosclerosis ; catalytic activity ; hyperinsulinemia ; hyperlipidemia ; inflammation ; lungs ; moieties ; neoplasms ; obesity ; pancreas ; phospholipase A2 ; phospholipases ; phospholipids ; respiratory tract diseases
    Language English
    Dates of publication 2019-06
    Size p. 784-788.
    Publishing place Elsevier B.V.
    Document type Article
    ISSN 1388-1981
    DOI 10.1016/j.bbalip.2018.07.001
    Database NAL-Catalogue (AGRICOLA)

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