Article
Sport Sciences
Massimo Teso, Alessandro L. Colosio, Silvia Pogliaghi
Summary: There is a mismatch between heart rate and metabolic intensity. Whenever exercise is prescribed based on heart rate, target values should be adjusted over time to maintain the desired metabolic stimulus.
MEDICINE & SCIENCE IN SPORTS & EXERCISE
(2022)
Article
Physiology
Rafael A. de Aguiar, Tiago Turnes, Fernando K. Borszcz, Joao A. G. Raimundo, Fabrizio Caputo
Summary: This study assessed the reliability of near-infrared spectroscopy-derived muscle oxygen uptake kinetics following running exercise and its relationship with parameters of aerobic fitness. The findings showed that the time constant of muscle oxygen uptake kinetics in the gastrocnemius presented good reliability and correlated with aerobic fitness parameters. Therefore, near-infrared spectroscopy-derived muscle oxidative capacity can be used to analyze the oxidative system on both local and systemic levels.
EXPERIMENTAL PHYSIOLOGY
(2022)
Article
Engineering, Mechanical
Liping Qi, Shuo Guan, Dong-Dong Zhou, Feng-Shan Gao, Li-Qing Liu
Summary: The study investigated the impact of muscle fiber type on the slow component of oxygen uptake kinetics and electromyographic activity in sprinters and endurance runners. The results showed significant differences in the slow component of VO2 between the two groups, with sprinters exhibiting higher amplitude and earlier onset compared to endurance runners. Electromyographic mean power frequency also increased significantly during the slow component phase.
PROCEEDINGS OF THE INSTITUTION OF MECHANICAL ENGINEERS PART C-JOURNAL OF MECHANICAL ENGINEERING SCIENCE
(2021)
Article
Physiology
Paulo Cesar do Nascimento Salvador, Eduardo Marcel Fernandes Nascimento, Diego Antunes, Luiz Guilherme Antonacci Guglielmo, Benedito Sergio Denadai
Summary: This study aimed to explain the V?O2${\dot{V}}_{{{\rm{O}}}_{\rm{2}}}$ slow component (V?O2sc${\dot{V}}_{{{\rm{O}}}_{\rm{2}}{\rm{sc}}}$) and muscle fatigue during high-intensity cycling. The findings suggest that muscle fatigue and the increase in oxygen cost have the same physiological cause, which is linked with a decrease in muscle oxygen consumption and a change in lactate accumulation. Muscle activation heterogeneity and metabolism of different muscles activated during cycling are associated with muscle fatigue and the V?O2sc${\dot{V}}_{{{\rm{O}}}_{\rm{2}}{\rm{sc}}}$.
EXPERIMENTAL PHYSIOLOGY
(2023)
Review
Sport Sciences
Richie P. P. Goulding, Mark Burnley, Rob C. I. Wust
Summary: The priming effect, which refers to the observation that prior heavy or severe-intensity exercise speeds overall oxygen uptake kinetics, has been extensively studied and its underlying mechanisms debated. This review examines the evidence for and against factors such as lactic acidosis, increased muscle temperature, oxygen delivery, altered motor unit recruitment patterns, and enhanced intracellular oxygen utilization in contributing to the priming effect. While lactic acidosis and increased muscle temperature are unlikely key factors, alterations in motor unit recruitment patterns and enhanced intracellular oxygen utilization appear to play important roles.
Article
Chemistry, Physical
Bedabyas Behera, Yuan-Pern Lee
Summary: This study investigated the mechanism and kinetics of the reaction between CH3CHOO and HC(O)OH. The results showed that this reaction has a large rate coefficient and produces hydroperoxyethyl formate and formic acetic anhydride as the end products. This research is important for further understanding the formation mechanism of secondary organic aerosols in the atmosphere.
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
(2023)
Article
Physiology
Hassan A. Rudayni, George Stephenson, Giuseppe S. Posterino
Summary: A method for directly measuring the transport of the fluorescent D-glucose analogue 2-NBDG across the plasma membrane of single skeletal muscle fibers has been developed. The study found that the transport of 2-NBDG and D-glucose in resting muscle fibers is fast and relies on GLUT-mediated transport. This suggests that the rate-limiting step in D-glucose uptake in skeletal muscle is not necessarily the GLUT-mediated transport of D-glucose.
Article
Chemistry, Medicinal
Hye-Won Yang, Seyeon Oh, Dong-Min Chung, Minyoung Seo, Shin Jae Park, You-Jin Jeon, Kyunghee Byun, BoMi Ryu
Summary: This study evaluated the effect of Ishige okamurae extract (IO) and its component, Ishophloroglucin A (IPA), on muscle atrophy induced by dexamethasone. The results showed that IO and IPA supplementation improved muscle weight and width, enhanced grip strength, and regulated muscle protein metabolism by modulating gene expression related to protein synthesis, degradation, and muscle growth activation or inhibition.
Article
Chemistry, Applied
Chaochen Tang, Bingzhi Jiang, Irsa Ejaz, Asif Ameen, Rong Zhang, Xueying Mo, Zhangying Wang
Summary: This study developed a high-throughput analysis method using near-infrared spectroscopy (NIRS) to determine the quality of sweet potato roots. It successfully established several optimal equations for various quality traits and demonstrated the feasibility of large-scale screening for elite germplasm in sweet potato breeding.
Article
Nutrition & Dietetics
Colleen S. Deane, Ushnah S. U. Din, Tanvir S. Sian, Ken Smith, Amanda Gates, Jonathan N. Lund, John P. Williams, Ricardo Rueda, Suzette L. Pereira, Philip J. Atherton, Bethan E. Phillips
Summary: Acute curcumin supplementation enhances the effect of oral nutritional supplement on microvascular blood flow in healthy older adults, without affecting muscle glucose uptake, vascular function, or blood flow.
Article
Agriculture, Multidisciplinary
Aoife C. Power, John Jones, Caoimhe NiNeil, Sive Geoghegan, Susan Warren, Sinead Currivan, Daniel Cozzolino
Summary: The study showed that NIR spectroscopy combined with PLS regression can classify whiskey samples and determine the level of adulteration. The potential of NIR with chemometric analysis as a rapid, portable, and non-destructive screening tool for quality control, traceability, and food/beverage adulteration for customs and regulatory agencies was highlighted.
JOURNAL OF THE SCIENCE OF FOOD AND AGRICULTURE
(2021)
Article
Plant Sciences
Zhou-Kang Li, Yu-Dong Chen, Jin-Long Wang, La-Mei Jiang, Yu-Xian Fan, Guang-Hui Lue
Summary: Through the study of the desert woody perennial plant Populus euphratica, it was found that female P. euphratica has a stronger capacity for water absorption and absorption speed compared to male P. euphratica, possibly due to differences in cell structure and osmotic regulatory substances in female leaves.
ENVIRONMENTAL AND EXPERIMENTAL BOTANY
(2023)
Article
Instruments & Instrumentation
Xiaoyun Chen, Kshitish A. Patankar, Matthew Larive
Summary: Polyurethane foams are widely used in various fields, and monitoring PU reactions with NIR HSI technology can effectively extract kinetics information. The advantages of NIR HSI over conventional FT-NIR systems include faster spectral acquisition time and higher spatial resolution.
APPLIED SPECTROSCOPY
(2021)
Article
Biochemistry & Molecular Biology
Yasukiyo Yoshioka, Ryunoshin Kono, Masaki Kuse, Yoko Yamashita, Hitoshi Ashida
Summary: This study investigated the active compounds in Myristica fragrans and their mechanism in promoting glucose uptake. The researchers found that myristicin, licarin B, ADDP, and ADTP were the active compounds that promoted GLUT4 translocation. Oral administration of Myristica fragrans extract suppressed post-prandial hyperglycemia in mice. Therefore, Myristica fragrans shows promise as a functional food for preventing post-prandial hyperglycemia and type 2 diabetes mellitus.
Article
Biochemistry & Molecular Biology
Ping Wu, Lin Chen, Jia Cheng, Yaxiong Pan, Xin Zhu, Lingsheng Bao, Wuying Chu, Jianshe Zhang
Summary: Fish skeletal muscles are composed of slow and fast muscles, which have differences in carbohydrate and lipid metabolism. Analysis of miRNAs revealed that more miRNAs inhibit the expression of target genes in slow muscles, which may contribute to the differences in glucose and lipid metabolism between muscles.
COMPARATIVE BIOCHEMISTRY AND PHYSIOLOGY A-MOLECULAR & INTEGRATIVE PHYSIOLOGY
(2021)
Article
Genetics & Heredity
Yoel Gofin, Laura Palmer Mackay, Keren Machol, Sundeep Keswani, Lorraine Potocki, Eleonora Di Gregorio, Valeria Giorgia Naretto, Alfredo Brusco, Andres Hernandez-Garcia, Daryl A. Scott
Summary: FGFRL1 encodes a transmembrane protein related to fibroblast growth factor receptors, inhibiting cell proliferation and promoting cell differentiation and adhesion. Deficiency in FGFRL1 may contribute to CDH development, but disruption of a single copy alone is insufficient to cause diaphragm defects.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
(2021)
Article
Genetics & Heredity
Tiana M. Scott, Ian M. Campbell, Andres Hernandez-Garcia, Seema R. Lalani, Pengfei Liu, Chad A. Shaw, Jill A. Rosenfeld, Daryl A. Scott
Summary: The diagnostic yield of clinical exome sequencing (ES) in CDH+ is 37%, supporting the use of ES in cases of suspected CDH+. These results also provide evidence for phenotypic expansions involving genes associated with ALG12-congenital disorder of glycosylation, Rubinstein-Taybi syndrome, Fanconi anaemia, Coffin-Siris syndrome, and FOXP1-related disorders in CDH development.
JOURNAL OF MEDICAL GENETICS
(2022)
Article
Genetics & Heredity
Francesca Clementina Radio, Kaifang Pang, Andrea Ciolfi, Michael A. Levy, Andres Hernandez-Garcia, Lucia Pedace, Francesca Pantaleoni, Zhandong Liu, Elke de Boer, Adam Jackson, Alessandro Bruselles, Haley McConkey, Emilia Stellacci, Stefania Lo Cicero, Marialetizia Motta, Rosalba Carrozzo, Maria Lisa Dentici, Kirsty McWalter, Megha Desai, Kristin G. Monaghan, Aida Telegrafi, Christophe Philippe, Antonio Vitobello, Margaret Au, Katheryn Grand, Pedro A. Sanchez-Lara, Joanne Baez, Kristin Lindstrom, Peggy Kulch, Jessica Sebastian, Suneeta Madan-Khetarpal, Chelsea Roadhouse, Jennifer J. MacKenzie, Berrin Monteleone, Carol J. Saunders, July K. Jean Cuevas, Laura Cross, Dihong Zhou, Taila Hartley, Sarah L. Sawyer, Fabiola Paoli Monteiro, Tania Vertemati Secches, Fernando Kok, Laura E. Schultz-Rogers, Erica L. Macke, Eva Morava, Eric W. Klee, Jennifer Kemppainen, Maria Iascone, Angelo Selicorni, Romano Tenconi, David J. Amor, Lynn Pais, Lyndon Gallacher, Peter D. Turnpenny, Karen Stals, Sian Ellard, Sara Cabet, Gaetan Lesca, Joset Pascal, Katharina Steindl, Sarit Ravid, Karin Weiss, Alison M. R. Castle, Melissa T. Carter, Louisa Kalsner, Bert B. A. de Vries, Bregje W. van Bon, Marijke R. Wevers, Rolph Pfundt, Alexander P. A. Stegmann, Bronwyn Kerr, Helen M. Kingston, Kate E. Chandler, Willow Sheehan, Abdallah F. Elias, Deepali N. Shinde, Meghan C. Towne, Nathaniel H. Robin, Dana Goodloe, Adeline Vanderver, Omar Sherbini, Krista Bluske, R. Tanner Hagelstrom, Caterina Zanus, Flavio Faletra, Luciana Musante, Evangeline C. Kurtz-Nelson, Rachel K. Earl, Britt-Marie Anderlid, Gilles Morin, Marjon van Slegtenhorst, Karin E. M. Diderich, Alice S. Brooks, Joost Gribnau, Ruben G. Boers, Teresa Robert Finestra, Lauren B. Carter, Anita Rauch, Paolo Gasparini, Kym M. Boycott, Tahsin Stefan Barakat, John M. Graham, Laurence Faivre, Siddharth Banka, Tianyun Wang, Evan E. Eichler, Manuela Priolo, Bruno Dallapiccola, Lisenka E. L. M. Vissers, Bekim Sadikovic, Daryl A. Scott, Jimmy Lloyd Holder, Marco Tartaglia
Summary: Deletion 1p36 (del1p36) syndrome is the most common human disorder caused by a terminal autosomal deletion, characterized by molecular and clinical heterogeneity. The loss of SPEN gene is associated with a neurodevelopmental disorder that significantly overlaps with features of del1p36 syndrome, including developmental delay, autism, anxiety, aggressive behavior, and more. SPEN haploinsufficiency is a major contributor to this disorder, with specific epigenetic effects on the X chromosome in affected females.
AMERICAN JOURNAL OF HUMAN GENETICS
(2021)
Article
Cell Biology
Ken Saida, Tokiko Fukuda, Daryl A. Scott, Toru Sengoku, Kazuhiro Ogata, Annarita Nicosia, Andres Hernandez-Garcia, Seema R. Lalani, Mahshid S. Azamian, Haley Streff, Pengfei Liu, Hongzheng Dai, Takeshi Mizuguchi, Satoko Miyatake, Miki Asahina, Tsutomu Ogata, Noriko Miyake, Naomichi Matsumoto
Summary: X-linked intellectual disability (XLID) is a common disorder with over 100 mutated genes reported. This study identified pathogenic OTUD5 variants in two families with developmental delay, showing features of LINKage-specific-deubiquitylation-deficiency-induced embryonic defects (LINKED) syndrome. Unlike previous reports of early lethality, the patients in this study have survived with a milder phenotype.
FRONTIERS IN CELL AND DEVELOPMENTAL BIOLOGY
(2021)
Letter
Physiology
Bhabuk Koirala, Alessandro Concas, Yi Sun, L. Bruce Gladden, Nicola Lai
JOURNAL OF APPLIED PHYSIOLOGY
(2022)
Article
Physics, Applied
Meimei Lai, Shutong Song, Edwin Oshin, Lucas Potter, Nicola Lai, Chunqi Jiang
Summary: The presence of biological materials can change the properties of plasma and affect the production of reactive oxygen and nitrogen species (RONS). Understanding these effects is important for the application of non-thermal atmospheric-pressure plasma jets in biomedical fields.
JOURNAL OF APPLIED PHYSICS
(2022)
Article
Genetics & Heredity
Amy Hardcastle, Aliska M. Berry, Ian M. Campbell, Xiaonan Zhao, Pengfei Liu, Amanda E. Gerard, Jill A. Rosenfeld, Saumya D. Sisoudiya, Andres Hernandez-Garcia, Sara Loddo, Silvia Di Tommaso, Antonio Novelli, Maria L. Dentici, Rossella Capolino, Maria C. Digilio, Ludovico Graziani, Cecilie F. Rustad, Katherine Neas, Giovanni B. Ferrero, Alfredo Brusco, Eleonora Di Gregorio, Diana Wellesley, Claire Beneteau, Madeleine Joubert, Kris Van den Bogaert, Anneleen Boogaerts, Dominic J. McMullan, John Dean, Maria G. Giuffrida, Laura Bernardini, Vinod Varghese, Nora L. Shannon, Rachel E. Harrison, Wayne W. K. Lam, Shane McKee, Peter D. Turnpenny, Trevor Cole, Jenny Morton, Jacqueline Eason, Marilyn C. Jones, Rebecca Hall, Michael Wright, Karen Horridge, Chad A. Shaw, Wendy K. Chung, Daryl A. Scott
Summary: This study utilized data from the DECIPHER database to identify the role of CREBBP, SMARCA4, UBA2, and USP9X genes in diaphragm development. It also discovered new phenotypic expansions.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
(2022)
Article
Biochemistry & Molecular Biology
Andres Hernandez-Garcia, Katherine E. Pendleton, Sangbae Kim, Yumei Li, Bum J. Kim, Hitisha P. Zaveri, Valerie K. Jordan, Aliska M. Berry, M. Cecilia Ljungberg, Rui Chen, Rainer B. Lanz, Daryl A. Scott
Summary: SOX7 is a gene encoding a transcription factor that is located in a region on chromosome 8p23.1, commonly deleted in individuals with ventricular septal defects (VSDs). The deficiency of SOX7 leads to hypocellular endocardial cushions and reduced endocardial-to-mesenchymal transition (EndMT). Furthermore, the interaction between SOX7 and Wnt4 plays a role in the development of VSDs through their additive effects on endocardial cushion development. The results provide additional evidence for the involvement of SOX7, Wnt4, and BMP2 in the pathogenesis of VSDs in humans.
HUMAN MOLECULAR GENETICS
(2023)
Article
Physiology
Bhabuk Koirala, Alessandro Concas, Yi Sun, L. Bruce Gladden, Nicola Lai
Summary: The relationship between skeletal muscle venous and NIRS signals suggests a main hemoglobin contribution, but computational evidence shows a significant contribution of myoglobin as well.
JOURNAL OF APPLIED PHYSIOLOGY
(2023)
Review
Chemistry, Medicinal
Agnieszka Sidorowicz, Giacomo Fais, Mattia Casula, Massimiliano Borselli, Giuseppe Giannaccare, Antonio Mario Locci, Nicola Lai, Roberto Orru, Giacomo Cao, Alessandro Concas
Summary: Microalgae have been used as a source of useful compounds for food and dietary supplements, as well as for the synthesis of nanoparticles through environmentally friendly routes. The occurrence of global health threats has brought attention to the application of microalgae in medicine. This review discusses the influence of secondary metabolites from microalgae on nanoparticle synthesis as therapeutics, as well as the use of isolated compounds on nanoparticles to combat diseases. However, further research is needed to fully understand the role of microalgae in the human body and translate lab-based research into clinical trials.
Article
Pediatrics
Katherine E. Pendleton, Andres Hernandez-Garcia, Jennifer M. Lyu, Ian M. Campbell, Chad A. Shaw, Julie Vogt, Frances A. High, Patricia K. Donahoe, Wendy K. Chung, Daryl A. Scott
Summary: FOXP1 encodes a transcription factor involved in tissue regulation and cell-type-specific functions. Haploinsufficiency of FOXP1 is associated with a neurodevelopmental disorder and structural birth defects. FOXP4 variants have also been shown to contribute to the development of congenital diaphragmatic hernia. FOXP proteins may function together or independently to regulate gene expression during diaphragm development. The development of CDH is influenced by a combination of FOXP1 and other factors.
JOURNAL OF PEDIATRIC GENETICS
(2023)
Article
Genetics & Heredity
Christina Y. Miyake, Saad A. Ehsan, Lilei Zhang, Samuel J. Mackenzie, Mahshid S. Azamian, Daryl A. Scott, Andres Hernandez-Garcia, Seema R. Lalani
Summary: TDD is caused by pathogenic biallelic variants in the TANGO2 gene, leading to delayed development, cognitive impairment, language deficits, and gait abnormalities. There is phenotypic variability among affected individuals, and early B-complex vitamin supplementation may play a role in preventing metabolic crises and improving neurologic outcomes in TDD.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A
(2023)
Article
Biochemistry & Molecular Biology
Ivy K. N. Chiang, David Humphrey, Richard J. Mills, Peter Kaltzis, Shikha Pachauri, Matthew Graus, Diptarka Saha, Zhijian Wu, Paul Young, Choon Boon Sim, Tara Davidson, Andres Hernandez-Garcia, Chad A. Shaw, Alexander Renwick, Daryl A. Scott, Enzo R. Porrello, Emily S. Wong, James E. Hudson, Kristy Red-Horse, Gonzalo del Monte-Nieto, Mathias Francois
Summary: The Sox7 transcription factor plays a critical role in instructing cardiac endothelium identity during ventricular chamber development. Loss of Sox7 function in mice results in cardiac ventricular defects and abnormal coronary artery formation. Sox7 maintains cardiac endothelial cell identity, which is crucial for ventricular compaction and coronary artery development.
Article
Biochemistry & Molecular Biology
Kamal Asadipour, Maisoun Bani Hani, Lucas Potter, Brittney L. Ruedlinger, Nicola Lai, Stephen J. Beebe
Summary: This study demonstrates that nanosecond pulsed electric fields (nsPEFs) can modulate cellular redox functions and metabolism by regulating trans-plasma membrane electron transport and mitochondrial electron transport system. The effects of nsPEFs on cells are dose-dependent, with low levels being beneficial and high levels causing damage.
BIOELECTROCHEMISTRY
(2024)
Meeting Abstract
Endocrinology & Metabolism
Yoel Gofin, Laura Palmer Mackay, Keren Machol, Sundeep Keswani, Lorraine Potocki, Eleonora Di Gregorio, Valeria Naretto, Alfredo Brusco, Andres Hernandez-Garcia, Daryl Scott
MOLECULAR GENETICS AND METABOLISM
(2021)