effects of aging
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2022 ◽  
Vol 296 ◽  
pp. 118784
Author(s):  
Yang Yang ◽  
Yemian Peng ◽  
Yibing Ma ◽  
Guojun Chen ◽  
Fangbai Li ◽  
...  

2022 ◽  
Vol 140 ◽  
pp. 106343
Author(s):  
Juhwan Kim ◽  
Donggeon Kwak ◽  
Jungjae Park ◽  
Takayuki Kubota ◽  
Taesung Kim

2022 ◽  
Vol 89 (S1) ◽  
pp. S23-S28
Author(s):  
Daniela Frasca ◽  
Suresh Pallikkuth ◽  
Savita Pahwa

Materials ◽  
2022 ◽  
Vol 15 (2) ◽  
pp. 620
Author(s):  
Yousef Jiries ◽  
Tamar Brosh ◽  
Shlomo Matalon ◽  
Vladimir Perlis ◽  
Zeev Ormianer

Aim: We assess the accuracy of torque controllers after several aging processes and the bacterial leakage on Implant-Abutment complexes (IAC).Methods: A total of 12 spring-type and 12 friction-type torque controllers and 48 IAC (24 conical and 24 hexagonal connections) were evaluated. Chemical, mechanical, temperature, and pressure-aging methods were applied individually to replicate clinical use. Torque controller accuracy was analyzed before and after aging using a calibrated gauge. To assess bacterial leakage, the IAC were suspended in a bacterial medium for 24 h. Direct Contact Test (DCT) and Polymerase Chain Reaction Test (RT-PCR) analyzed the infiltration of F. nucleatum and P. gingivalis into the IAC micro-gap. Results: A significant decrease in torque after 10 days of aging was found. The spring-type torque controller was affected the most, regardless of the aging method (P < 0.05). PCR results indicated that all groups exhibited significantly more bacterial leakage, regardless of the method used (P < 0.05). The conical IAC demonstrated more bacterial leakage of P. gingivalis compared with the hexagonal IAC (P = 0.07). DCT found bacterial growth in the IAC only before aging and was not identified after aging. Conclusion: Aging affects torque accuracy. A reduction in force was noticed after 10 days. The conical IAC exhibits more bacterial leakage, although this was not statistically significant.


2022 ◽  
Author(s):  
Sarah Anne Sauvé ◽  
Jeremy Marozeau ◽  
Benjamin Zendel

Auditory stream segregation, or separating sounds into their respective sources, and tracking them over time is a fundamental auditory ability. Previous research has separately explored the impacts of aging and musicianship on the ability to separate and follow auditory streams. The current study evaluated the simultaneous effects of age and musicianship on auditory streaming induced by three physical features: intensity, spectral envelope and temporal envelope. In the first study, older and younger musicians and non-musicians with normal hearing identified deviants in a four-note melody interleaved with distractors that were more or less similar to the melody in terms of intensity, spectral envelope and temporal envelope. In the second study, older and younger musicians and non-musicians participated in a dissimilarity rating paradigm with pairs of melodies that differed along the same three features. Results suggested that auditory streaming skills are maintained in older adults but that older adults rely on intensity more than younger adults while musicianship is associated with increased sensitivity to spectral and temporal envelope, acoustic features that are typically less effective for stream segregation, particularly in older adults.


2022 ◽  
Vol 12 ◽  
Author(s):  
Hiroshi Nishiura ◽  
Mai Imasaka ◽  
Koji Yamanegi ◽  
Jiro Fujimoto ◽  
Masaki Ohmuraya

Almost all mature cells that undergo apoptosis in an age-dependent or an accidental manner are completely recovered in tissue-specific microenvironments without any physiological changes. After peripheral blood leukocytes are released into the local region, fibroblast cells and new blood vessels commonly proliferate during wound healing. Inducible repair tools mainly supplied from blood vessels are cleared by peripheral blood phagocytic macrophages. Finally, hematopoietic stem cell (HSC)-derived precursor cells migrate from bone marrow (BM) to the microenvironment to rebuild damaged tissues (the mature immune system). In contrast to the mature immune system, the effects of aging on HSCs (long-term HSCs) and peripheral blood lymphocytes (long-term PBLs) are not clearly understood in the BM and thymus niches with tissue-specific microenvironments with some physiological changes (the aged BM niche) for incomplete rebuilding of damaged tissues (the aged immune system). In this review, the roles of the aged immune system in both a delay of acute inflammation and the development of chronic inflammation or fibrosis are discussed.


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