102 research outputs found
The Neural Basis of Love as a Subliminal Prime: An Event-related Functional Magnetic Resonance Imaging Study
- Publication venue
- 'MIT Press - Journals'
- Publication date
- Field of study
Control of Tungiasis through Intermittent Application of a Plant-Based Repellent: An Intervention Study in a Resource-Poor Community in Brazil
- Author
- B Winter
- CM Lins Calheiros
- D Pilger
- DD Chadee
- H Feldmeier
- H Feldmeier
- H Feldmeier
- H Feldmeier
- H Feldmeier
- H Feldmeier
- H Mashek
- Hermann Feldmeier
- J Heukelbach
- J Heukelbach
- J Heukelbach
- J Heukelbach
- J Heukelbach
- J Heukelbach
- J Litvoc
- James S. McCarthy
- JD Kehr
- JK Joseph
- John Buckendahl
- Judith Dorothea Kehr
- Jörg Heukelbach
- L Ariza
- Liana Ariza
- M Eisele
- M Muehlen
- MA Ade-Serrano
- Martin Seidenschwang
- RS Matias
- RW de Carvalho
- S Schwalfenberg
- T Wilcke
- US Ugbomoiko
- Publication venue
- Public Library of Science
- Publication date
- 09/11/2010
- Field of study
Tungiasis is a parasitic skin disease caused by the female sand flea Tunga penetrans. The disease is frequent in resource-poor communities in South America and sub-Saharan Africa and affects the poorest of the poor. Sand flea disease is associated with a considerable morbidity and may lead to tetanus in non-vaccinated individuals. The degree of morbidity depends on the intensity of infestation, i.e., the number of embedded sand fleas a person has. Since tungiasis is a zoonosis involving a host of animal reservoirs, and because an effective treatment is not at hand, in resource-poor settings elimination is not feasible. Preventing morbidity to develop is therefore the only means to protect exposed individuals from sand flea disease. Similar to other arthropods, sand fleas can be repelled before they penetrate into the skin. In this study we show that the intermittent application of a plant-based repellent, of which the major component is coconut oil, reduces the intensity of infestation dramatically during the whole transmission season and prevents tungiasis-associated morbidity from developing. The prevention can be performed at the household level by the affected individuals themselves with minimal input from the health sector
Effects of Male Hypogonadism on Regional Adipose Tissue Fatty Acid Storage and Lipogenic Proteins
- Author
- AM Hall
- B Berenguer
- C Koutsari
- C-LE Yen
- CC Allred
- CM Harmon
- DA Schoeller
- DG Mashek
- HZ Pomerantz
- J Folch
- J Knudsen
- JA Hamilton
- JCK Wells
- JM Elbers
- JM Tanner
- Jose A. L. Calbet
- KN Frayn
- MD Jensen
- MD Jensen
- ME Ramirez
- Michael D. Jensen
- N Mauras
- P Marin
- P Marin
- P Marin
- P Nilsson-Ehle
- PJ Snyder
- RC Causon
- S Santosa
- S Shadid
- SA Romanski
- SA Romanski
- SB Votruba
- SM Humphreys
- Sylvia Santosa
- X-MT Persson
- XG Hou
- YD Tchoukalova
- Z Sfeir
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
Testosterone has long been known to affect body fat distribution, although the underlying mechanisms remain elusive. We investigated the effects of chronic hypogonadism in men on adipose tissue fatty acid (FA) storage and FA storage factors. Twelve men with chronic hypogonadism and 13 control men matched for age and body composition: 1) underwent measures of body composition with dual energy x-ray absorptiometry and an abdominal CT scan; 2) consumed an experimental meal containing [3H]triolein to determine the fate of meal FA (biopsy-measured adipose storage vs. oxidation); 3) received infusions of [U-13C]palmitate and [1-14C]palmitate to measure rates of direct free (F)FA storage (adipose biopsies). Adipose tissue lipoprotein lipase, acyl-CoA synthetase (ACS), and diacylglycerol acetyl-transferase (DGAT) activities, as well as, CD36 content were measured to understand the mechanism by which alterations in fat storage occur in response to testosterone deficiency. Results of the study showed that hypogonadal men stored a greater proportion of both dietary FA and FFA in lower body subcutaneous fat than did eugonadal men (both p<0.05). Femoral adipose tissue ACS activity was significantly greater in hypogonadal than eugonadal men, whereas CD36 and DGAT were not different between the two groups. The relationships between these proteins and FA storage varied somewhat between the two groups. We conclude that chronic effects of testosterone deficiency has effects on leg adipose tissue ACS activity which may relate to greater lower body FA storage. These results provide further insight into the role of androgens in body fat distribution and adipose tissue metabolism in humans
Palmitoleate Induces Hepatic Steatosis but Suppresses Liver Inflammatory Response in Mice
- Author
- A Lonardo
- AA Wendel
- AJ Sanyal
- BA Neuschwander-Tetri
- C Wu
- C Wu
- C Wu
- Chaodong Wu
- D Cai
- D Mozaffarian
- DE Kelley
- Douglas G. Mashek
- E Tauriainen
- Fuer Lu
- G Marchesini
- GC Farrell
- H Cao
- H Tilg
- H Tilg
- Hang Xu
- Honggui Li
- Huan Wang
- Hui Dong
- I Shimomura
- J Gong
- J Zhang
- JD Browning
- JI Odegaard
- Jianping Ye
- JM Petit
- Kuok Teong Ong
- Lai Wei
- M Monetti
- M Sekiya
- P Angulo
- P Puri
- R Dentin
- Rosemary L. Walzem
- S Joshi-Barve
- S Nakamura
- Shih-Lung Woo
- SY Bu
- Vera Halim
- VT Samuel
- Weiyu Zhang
- X Guo
- X Liu
- Xin Guo
- Y Akazawa
- Y Huo
- Y Huo
- Yuqing Huo
- Z Deng
- ZH Yang
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2012
- Field of study
The interaction between fat deposition and inflammation during obesity contributes to the development of non-alcoholic fatty liver disease (NAFLD). The present study examined the effects of palmitoleate, a monounsaturated fatty acid (16â¶1n7), on liver metabolic and inflammatory responses, and investigated the mechanisms by which palmitoleate increases hepatocyte fatty acid synthase (FAS) expression. Male wild-type C57BL/6J mice were supplemented with palmitoleate and subjected to the assays to analyze hepatic steatosis and liver inflammatory response. Additionally, mouse primary hepatocytes were treated with palmitoleate and used to analyze fat deposition, the inflammatory response, and sterol regulatory element-binding protein 1c (SREBP1c) activation. Compared with controls, palmitoleate supplementation increased the circulating levels of palmitoleate and improved systemic insulin sensitivity. Locally, hepatic fat deposition and SREBP1c and FAS expression were significantly increased in palmitoleate-supplemented mice. These pro-lipogenic events were accompanied by improvement of liver insulin signaling. In addition, palmitoleate supplementation reduced the numbers of macrophages/Kupffer cells in livers of the treated mice. Consistently, supplementation of palmitoleate decreased the phosphorylation of nuclear factor kappa B (NF-ÎșB, p65) and the expression of proinflammatory cytokines. These results were recapitulated in primary mouse hepatocytes. In terms of regulating FAS expression, treatment of palmitoleate increased the transcription activity of SREBP1c and enhanced the binding of SREBP1c to FAS promoter. Palmitoleate also decreased the phosphorylation of NF-ÎșB p65 and the expression of proinflammatory cytokines in cultured macrophages. Together, these results suggest that palmitoleate acts through dissociating liver inflammatory response from hepatic steatosis to play a unique role in NAFLD
Relation of DNA Methylation of 5âČ-CpG Island of ACSL3 to Transplacental Exposure to Airborne Polycyclic Aromatic Hydrocarbons and Childhood Asthma
- Author
- A Kuzmin
- A Wijga
- AR Khaled
- B Jones
- Catherine M. Suter
- CG Van Horn
- D-U Lee
- DC Dolinoy
- Deliang Tang
- DG Mashek
- DK Das
- E Bouzigon
- E Gyorffy
- FP Perera
- Frederica Perera
- GS Prins
- H Minekura
- J Liu
- JG Herman
- Julie Herbstman
- L Hilakivi-Clarke
- Linda Levin
- LO Tykocinski
- M Beck
- M Mannino
- M Miyazaki
- M Tomita
- M Wu
- MD Anway
- MK Selgrade
- MS Perzanowski
- NJ Faergeman
- P Weber
- RA Coleman
- Rachel Miller
- RI Aqeilan
- RK Woods
- RL Miller
- RL Miller
- RP Birkenbihl
- RW Godschalk
- S Agarwal
- S Choudhry
- S Li
- Shuk-mei Ho
- SM Ho
- SM Ho
- SW Nicholas
- T Fujino
- T Mashima
- TA Mori
- TH Huang
- V Padmanabhan
- W Jedrychowski
- W Stock
- Wan-yee Tang
- WH Oddy
- WY Tang
- WY Tang
- Publication venue
- Public Library of Science
- Publication date
- 01/01/2009
- Field of study
In a longitudinal cohort of âŒ700 children in New York City, the prevalence of asthma (>25%) is among the highest in the US. This high risk may in part be caused by transplacental exposure to traffic-related polycyclic aromatic hydrocarbons (PAHs) but biomarkers informative of PAH-asthma relationships is lacking. We here hypothesized that epigenetic marks associated with transplacental PAH exposure and/or childhood asthma risk could be identified in fetal tissues. Mothers completed personal prenatal air monitoring for PAH exposure determination. Methylation sensitive restriction fingerprinting was used to analyze umbilical cord white blood cell (UCWBC) DNA of 20 cohort children. Over 30 DNA sequences were identified whose methylation status was dependent on the level of maternal PAH exposure. Six sequences were found to be homologous to known genes having one or more 5âČ-CpG island(s) (5âČ-CGI). Of these, acyl-CoA synthetase long-chain family member 3 (ACSL3) exhibited the highest concordance between the extent of methylation of its 5âČ-CGI in UCWBCs and the level of gene expression in matched fetal placental tissues in the initial 20 cohort children. ACSL3 was therefore chosen for further investigation in a larger sample of 56 cohort children. Methylation of the ACSL3 5âČ-CGI was found to be significantly associated with maternal airborne PAH exposure exceeding 2.41 ng/m3 (ORâ=â13.8; p<0.001; sensitivityâ=â75%; specificityâ=â82%) and with a parental report of asthma symptoms in children prior to age 5 (ORâ=â3.9; p<0.05). Thus, if validated, methylated ACSL3 5âČCGI in UCWBC DNA may be a surrogate endpoint for transplacental PAH exposure and/or a potential biomarker for environmentally-related asthma. This exploratory report provides a new blueprint for the discovery of epigenetic biomarkers relevant to other exposure assessments and/or investigations of exposure-disease relationships in birth cohorts. The results support the emerging theory of early origins of later life disease development
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)
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- A. -G. Wu
- A. C. Ma
- A. K. Au
- Abdel-Aziz A. K.
- Abdelfatah S.
- Abdellatif M.
- Abdoli A.
- Abel S.
- Abeliovich H.
- Abildgaard M. H.
- Abudu Y. P.
- Acevedo-Arozena A.
- Adamopoulos I. E.
- Adeli K.
- Adolph T. E.
- Adornetto A.
- Aflaki E.
- Agam G.
- Agarwal A.
- Aggarwal B. B.
- Agnello M.
- Agostinis P.
- Agrewala J. N.
- Agrotis A.
- Aguilar P. V.
- Ahmad S. T.
- Ahmed Z. M.
- Ahumada-Castro U.
- Aits S.
- Aizawa S.
- Akkoc Y.
- Akoumianaki T.
- Akpinar H. A.
- Al-Abd A. M.
- Al-Akra L.
- Al-Gharaibeh A.
- Alaoui-Jamali M. A.
- Alberti S.
- Alcocer-Gomez E.
- Alessandri C.
- Ali M.
- Alim Al-Bari M. A.
- Aliwaini S.
- Alizadeh J.
- Almacellas E.
- Almasan A.
- Alonso A.
- Alonso G. D.
- Altan-Bonnet N.
- Altieri D. C.
- Alvarez E. M. C.
- Alves da Costa C.
- Alves S.
- Alzaharna M. M.
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- Ambrosio S.
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- Ammanathan V.
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- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
Guidelines for the use and interpretation of assays for monitoring autophagy (4th edition)1.
- Author
- Abdel-Aziz AK
- Abdelfatah S
- Abdellatif M
- Abdoli A
- Abel S
- Abeliovich H
- Abildgaard MH
- Abudu YP
- Acevedo-Arozena A
- Adamopoulos IE
- Adeli K
- Adolph TE
- Adornetto A
- Aflaki E
- Agam G
- Agarwal A
- Aggarwal BB
- Agnello M
- Agostinis P
- Agrewala JN
- Agrotis A
- Aguilar PV
- Ahmad ST
- Ahmed ZM
- Ahumada-Castro U
- Aits S
- Aizawa S
- Akkoc Y
- Akoumianaki T
- Akpinar HA
- Al-Abd AM
- Al-Akra L
- Al-Gharaibeh A
- Alaoui-Jamali MA
- Alberti S
- Alcocer-GĂłmez E
- Alessandri C
- Ali M
- Alim Al-Bari MA
- Aliwaini S
- Alizadeh J
- Almacellas E
- Almasan A
- Alonso A
- Alonso GD
- Altan-Bonnet N
- Altieri DC
- Alves da Costa C
- Alves S
- Alzaharna MM
- Amadio M
- Amantini C
- Amaral C
- Ambrosio S
- Amer AO
- Ammanathan V
- An Z
- Andersen SU
- Andrabi SA
- Andrade-Silva M
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- Angelini S
- Ann D
- Anozie UC
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- Ălvarez ĂMC
- Ăvalos Y
- Ănal G
- ĂstĂŒn S
- ÄoliÄ M
- ÄokiÄ J
- Ćœerovnik E
- Publication venue
- 'Informa UK Limited'
- Publication date
- 01/01/2021
- Field of study
In 2008, we published the first set of guidelines for standardizing research in autophagy. Since then, this topic has received increasing attention, and many scientists have entered the field. Our knowledge base and relevant new technologies have also been expanding. Thus, it is important to formulate on a regular basis updated guidelines for monitoring autophagy in different organisms. Despite numerous reviews, there continues to be confusion regarding acceptable methods to evaluate autophagy, especially in multicellular eukaryotes. Here, we present a set of guidelines for investigators to select and interpret methods to examine autophagy and related processes, and for reviewers to provide realistic and reasonable critiques of reports that are focused on these processes. These guidelines are not meant to be a dogmatic set of rules, because the appropriateness of any assay largely depends on the question being asked and the system being used. Moreover, no individual assay is perfect for every situation, calling for the use of multiple techniques to properly monitor autophagy in each experimental setting. Finally, several core components of the autophagy machinery have been implicated in distinct autophagic processes (canonical and noncanonical autophagy), implying that genetic approaches to block autophagy should rely on targeting two or more autophagy-related genes that ideally participate in distinct steps of the pathway. Along similar lines, because multiple proteins involved in autophagy also regulate other cellular pathways including apoptosis, not all of them can be used as a specific marker for bona fide autophagic responses. Here, we critically discuss current methods of assessing autophagy and the information they can, or cannot, provide. Our ultimate goal is to encourage intellectual and technical innovation in the field
Effect of crude degummed canola oil and ad libitumgrazing on plasma metabolites of primiparous Holstein-Friesian cows in a pasture-based system
- Author
- A Adewuyi
- A Hayirli
- A Meikle
- AA Hamama
- Aduli E O Malau-Aduli
- Bunmi S Malau-Aduli
- C Lopes
- C Staples
- C Vlahakis
- CM Howlett
- CR Stockdale
- D Bauchart
- D Carroll
- D Hawkins
- D LaCount
- D Mashek
- D Wathes
- DE Bauman
- DPI
- G Douglas
- G Khorasani
- G Schroeder
- GR Khorasani
- I Del Galdo
- J Bottger
- J Moran
- J Roche
- J Sutton
- JB Andersen
- JK Drackley
- JK Drackley
- JLMR Leroy
- John R Otto
- K Duske
- L Delbecchi
- M Colazo
- MC De Vries
- MW Chichlowski
- Peter Nish
- PK Chelikani
- PV Van Soest
- R Bellows
- R Grummer
- R Grummer
- R Heitmann
- Razaq O Balogun
- RN Funston
- S Beam
- T Jenkins
- TA Miettinen
- W Butler
- W Butler
- WP Weiss
- Y Chilliard
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
Effect of unsaturated fatty acid supplementation on digestion, metabolism and nutrient balance in dairy cows during the transition period and early lactation
- Author
- Allen M. S.
- Bateman H. G.
- Bell A. W.
- Ben Salem H.
- Butler W. R.
- Casali A. O.
- Chen G.
- Chen X. B.
- Corl B. A.
- Czerkawski J. W.
- Doreau M.
- Doreau M.
- Drackley J. K.
- Erwin E. S.
- FlĂĄvio Garcia Vilela
- Folch J.
- Foldager J.
- Francisco Palma RennĂł
- Friggens N. C.
- Gozho G. N.
- Grum D. E.
- Grummer R. R.
- Hall M. B.
- Harvatine K. J.
- Huang Y.
- Ingvartsen K. L.
- Jefferson Rodrigues Gandra
- Jenkins T. C.
- Jenkins T. C.
- Jenkins T. C.
- JosĂ© Esler de Freitas JĂșnior
- Kramer J. K. G.
- Lenita Camargo Verdurico
- Luciana NavajĂĄs RennĂł
- Mashek D. G.
- Milton Maturana Filho
- Moallem U.
- Nocek J. E.
- Onetti S. G.
- Orellana Boero P.
- Overton T. R.
- Palmquist D.
- Palmquist D. L.
- Palmquist D. L.
- Petit H. V.
- Piperova L. S.
- Quigley J. D.
- Rabiee A. R.
- Rafael Villela Barletta
- Skaar T. C.
- Sniffen C. J.
- Ueda K.
- Van Knegsel A. T.
- Van Soest P. J.
- Van Soest P. J.
- Verdouw H.
- Weiss W. P.
- Zheng H. C.
- Publication venue
- 'FapUNIFESP (SciELO)'
- Publication date
- Field of study
Study protocol for a web-based personalized normative feedback alcohol intervention for young adult veterans
- Author
- A Aron
- AD Berkowitz
- AG Sadler
- B Borsari
- BF Grant
- C Erbes
- C Neighbors
- C Neighbors
- C Neighbors
- C Neighbors
- C Neighbors
- C Neighbors
- C Neighbors
- CF Turner
- CJ Monahan
- CM Simon-Arndt
- CT Nagoshi
- CW Hoge
- CW Kahler
- CW Kahler
- D Lewis
- D Mashek
- D Vogt
- DE Ramo
- DJ Brief
- DJ Brief
- DL Thombs
- DM Doumas
- E Vasilyeva
- EJ Hawkins
- ER Pedersen
- ER Pedersen
- Eric R. Pedersen
- F Griffiths
- Grant N. Marshall
- GT Lapham
- H Riper
- HR White
- HW Perkins
- I Burnett-Zeigler
- IM Geisner
- J Grossbard
- J Kramer
- J Williams
- JB Saunders
- JM Cronce
- JP Read
- JP Read
- JS Baer
- JW LaBrie
- K Bradley
- K Kroenke
- K Kypri
- KA Bradley
- KB Carey
- KB Carey
- KB Dotson
- KH Seal
- KK Chan
- LR Tropp
- LW Galen
- M Kulesza
- MA Cucciare
- MA Cucciare
- MA Lewis
- MA Lewis
- MA Lewis
- MA Lewis
- MA Lewis
- MA Lewis
- MA Stahre
- MB Miller
- MB Reed
- MD Wood
- MD Wood
- ME Larimer
- ME Larimer
- ME Larimer
- ME McDevitt-Murphy
- ME McDevitt-Murphy
- ML Cooper
- MP Martens
- MR Pemberton
- NA Sayer
- NM Petry
- P Britton
- P Farvolden
- PC Ouimette
- PD Bliese
- PS Calhoun
- R Mychasiuk
- R Ramchand
- RK Hester
- RL Collins
- RM Bray
- RM Bray
- S Darke
- SE McCabe
- ST Chermack
- ST Walters
- ST Walters
- Terry L. Schell
- TF Babor
- TF Babor
- TS Wells
- Publication venue
- 'Springer Science and Business Media LLC'
- Publication date
- Field of study
- âŠ