Neural Mechanisms of Nonauditory Effects of Noise Exposure on Special Populations.

Due to the abnormal structure and function of brain neural networks in special populations, such as children, elderly individuals, and individuals with mental disorders, noise exposure is more likely to have negative psychological and cognitive nonauditory effects on these individuals. There are unique and complex neural mechanisms underlying this phenomenon. For individuals with mental disorders, there are anomalies such as structural atrophy and decreased functional activation in brain regions involved in emotion and cognitive processing, such as the prefrontal cortex (PFC). Noise exposure can worsen these abnormalities in relevant brain regions, further damaging neural plasticity and disrupting normal connections and the transmission of information between the PFC and other brain areas by causing neurotransmitter imbalances. In the case of children, in a noisy environment, brain regions such as the left inferior frontal gyrus and PFC, which are involved in growth and development, are more susceptible to structural and functional changes, leading to neurodegenerative alterations. Furthermore, noise exposure can interrupt auditory processing neural pathways or impair inhibitory functions, thus hindering children's ability to map sound to meaning in neural processes. For elderly people, age-related shrinkage of brain regions such as the PFC, as well as deficiencies in hormone, neurotransmitter, and nutrient levels, weakens their ability to cope with noise. Currently, it is feasible to propose and apply coping strategies to improve the nonauditory effects of noise exposure on special populations based on the plasticity of the human brain.

The mechanism of phonetic information in voice identity discrimination: a comparative study based on sighted and blind people.

Purpose: The purpose of this study is to examine whether phonetic information functions and how phonetic information affects voice identity processing in blind people. Method: To address the first inquiry, 25 normal sighted participants and 30 blind participants discriminated voice identity, when listening forward speech and backward speech from their own native language and another unfamiliar language. To address the second inquiry, combining articulatory suppression paradigm, 26 normal sighted participants and 26 blind participants discriminated voice identity, when listening forward speech from their own native language and another unfamiliar language. Results: In Experiment 1, not only in the voice identity discrimination task with forward speech, but also in the discrimination task with backward speech, both the sighted and blind groups showed the superiority of the native language. This finding supports the view that backward speech still retains some phonetic information, and indicates that phonetic information can affect voice identity processing in sighted and blind people. In addition, only the superiority of the native language of sighted people was regulated by the speech manner, which is related to articulatory rehearsal. In Experiment 2, only the superiority of the native language of sighted people was regulated by articulatory suppression. This indicates that phonetic information may act in different ways on voice identity processing in sighted and blind people. Conclusion: The heightened dependence on voice source information in blind people appears not to undermine the function of phonetic information, but it appears to change the functional mechanism of phonetic information. These findings suggest that the present phonetic familiarity model needs to be improved with respect to the mechanism of phonetic information.

Cognitive and neural mechanisms of voluntary versus forced language switching in Chinese-English bilinguals: an fMRI study.

The ecological validity of bilingual code-switching has garnered increasing attention in recent years. Contrary to traditional studies that have focused on forced language switching, emerging theories posit that voluntary switching may not incur such a cost. To test these claims and understand differences between forced and voluntary switching, the present study conducted a systematic comparison through both behavioral and neural perspectives. Utilizing fMRI alongside picture-naming tasks, our findings diverge from prior work. Voluntary language switching not only demonstrated switching costs at the behavioral level but also significantly activated brain regions associated with inhibitory control. Direct comparisons of voluntary and forced language switching revealed no significant behavioral differences in switching costs, and both shared several common brain regions that were activated. On the other hand, a nuanced difference between the two types of language switching was revealed by whole-brain analysis: voluntary switching engaged fewer language control regions than forced switching. These findings offer a comprehensive view of the neural and behavioral dynamics involved in bilingual language switching, challenging prior claims that voluntary switching imposes no behavioral or neural costs, and thus providing behavioral and neuroimaging evidence for the involvement of inhibitory control in voluntary language switching.

16p11.2 CNV gene Doc2α functions in neurodevelopment and social behaviors through interaction with Secretagogin.

Copy-number variations (CNVs) of the human 16p11.2 genetic locus are associated with neurodevelopmental disorders, including autism spectrum disorders (ASDs) and schizophrenia. However, it remains largely unclear how this locus is involved in the disease pathogenesis. Doc2α is localized within this locus. Here, using in vivo and ex vivo electrophysiological and morphological approaches, we show that Doc2α-deficient mice have neuronal morphological abnormalities and defects in neural activity. Moreover, the Doc2α-deficient mice exhibit social and repetitive behavioral deficits. Furthermore, we demonstrate that Doc2α functions in behavioral and neural phenotypes through interaction with Secretagogin (SCGN). Finally, we demonstrate that SCGN functions in social/repetitive behaviors, glutamate release, and neuronal morphology of the mice through its Doc2α-interacting activity. Therefore, Doc2α likely contributes to neurodevelopmental disorders through its interaction with SCGN.

Constitutive Analysis and Microstructure Characteristics of As-Homogenized 2198 Al-Li Alloy under Different Hot Compression Deformation Conditions.

The 2198 Al-Li alloy has unique superiority in mechanical performance and has been extensively used in the aerospace field. In this study, the hot deformation behavior of the 2198 Al-Li alloy was investigated on a Gleeble-1500 thermomechanical simulator with a strain rate of 0.01-10 s-1 in the temperature range of 330-510 °C. The Arrhenius constitutive equation of the alloy was established based on the true stress-strain curves to describe the rheology behaviors during the deformation of the alloy. The processing maps under the strain of 0.2-0.8 were constructed, which indicates the efficiency of power dissipation and instability of the deformed alloy. It was found that the instability domains are more likely to occur in the regions of low deformation temperature and high strain rate, corresponding to the high Zener-Hollomon (Z) parameter. The microstructure evolution of the studied alloy with different Z parameters was characterized. Then, the dynamic recrystallization (DRX) behavior was studied by electron backscatter diffraction, and the misorientation angle of deformed specimens was analyzed. The effect of different deformation temperatures and strain rates on the microstructure of the alloy and the behavior of dislocations and precipitations were investigated by transmission electron microscopy. The results demonstrate that continuous dynamic recrystallization (CDRX) and geomatic dynamic recrystallization (GDRX) mainly occur at the deformation conditions of a low Z value, and discontinuous dynamic recrystallization (DDRX) is likely to occur with increasing Z values.

Identification of key pharmacological components and targets for Aidi injection in the treatment of pancreatic cancer by UPLC-MS, network pharmacology, and in vivo experiments.

BACKGROUND: Pancreatic cancer is one of the most lethal cancers worldwide. Aidi injection (ADI) is a representative antitumor medication based on Chinese herbal injection, but its antitumor mechanisms are still poorly understood. MATERIALS AND METHODS: In this work, the subcutaneous xenograft model of human pancreatic cancer cell line Panc-1 was established in nude mice to investigate the anticancer effect of ADI in vivo. We then determined the components of ADI using ultra-performance liquid chromatography-tandem mass spectrometry (UPLC-MS) and explored the possible molecular mechanisms against pancreatic cancer using network pharmacology. RESULTS: In vivo experiments, the volume, weight, and degree of histological abnormalities of implanted tumors were significantly lower in the medium and high concentration ADI injection groups than in the control group. Network pharmacology analysis identified four active components of ADI and seven key targets, TNF, VEGFA, HSP90AA1, MAPK14, CASP3, P53 and JUN. Molecular docking also revealed high affinity between the active components and the target proteins, including Astragaloside IV to P53 and VEGFA, Ginsenoside Rb1 to CASP3 and Formononetin to JUN. CONCLUSION: ADI could reduce the growth rate of tumor tissue and alleviate the structural abnormalities in tumor tissue. ADI is predicted to act on VEGFA, P53, CASP3, and JUN in ADI-mediated treatment of pancreatic cancer.

Core-Shell-Structured Particle Reinforced A356 Matrix Composite Prepared by Powder-Thixoforming: Effect of Reheating Temperature.

A novel core-shell-structured Ti-(Al-Si-Ti) particle (Ti-(Al-Si-Ti)p) reinforced A356 matrix composite was fabricated by a new method, powder thixoforming, which combines the merits of both powder metallurgy and semisolid thixoforming. The effects of reheating temperature on the microstructure and tensile properties of the resulting composite were investigated. The results indicated that the thickening of the Al-Si-Ti compound shells, with rising the reheating temperature, significantly enhanced the strengthening role, but the fracture and peeling of the shells, at higher than 600 °C, impaired the strengthening effect. The composite formed at 600 °C had a favorable tensile elongation of 8.3% besides high tensile strengths. During tensile testing, the Ti@(Al-Si-Ti)p frequently fractured across the Ti cores and occasionally cracked around the Ti cores, but preferentially fractured between the outer cracked shells and the inner cores for the composites thixoformed at higher than 600 °C. The delayed formation of cracks in the Ti-(Al-Si-Ti)p and the small size of the cracks contributed to ductility improvement. The MSL model, modified according to the Ti@(Al-Si-Ti)p characteristics, was essentially suitable for predicting the yield strength of such composites. The largest contribution to the strength was resulted from solid solution strengthening of Ti element, but the strengthening role from geometrically necessary dislocations was significantly improved as the reheating temperature rose from 590 °C to 600 °C.