Transcutaneous Auricular Vagus Nerve Stimulation Alleviates Monobenzone-Induced Vitiligo in Mice.

Vitiligo is a complex skin disorder that involves oxidative stress and inflammatory responses and currently lacks a definitive cure. Transcutaneous auricular vagus nerve stimulation (taVNS) is a noninvasive method for targeting the auricular branch of the vagus nerve and has gained widespread attention for potential intervention in the autonomic nervous system. Although previous research has suggested that vagus nerve stimulation can potentially inhibit inflammatory responses, its specific role and mechanisms in vitiligo treatment remain unknown. This study aimed to explore the therapeutic effects of taVNS in a mouse model of vitiligo induced by monobenzone. Initially, a quantitative assessment of the treatment effects on vitiligo mice was conducted using a scoring system, revealing that taVNS significantly alleviated symptoms, particularly by reducing the depigmented areas. Subsequent immunohistochemical analysis revealed the impact of taVNS treatment on melanocyte granules, mitigating pigment loss in the skin of monobenzone-induced vitiligo mice. Further analysis indicated that taVNS exerted its therapeutic effects through multiple mechanisms, including the regulation of oxidative stress, enhancement of antioxidant capacity, promotion of tyrosine synthesis, and suppression of inflammatory responses. The conclusions of this study not only emphasize the potential value of taVNS in vitiligo therapy, but also lay a foundation for future research into the mechanisms and clinical applications of taVNS.

Drivers of phenotypic variation in cartilage: Circadian clock genes.

Endogenous homeostasis and peripheral tissue metabolism are disrupted by irregular fluctuations in activation, movement, feeding and temperature, which can accelerate negative biological processes and lead to immune reactions, such as rheumatoid arthritis (RA) and osteoarthritis (OA). This review summarizes abnormal phenotypes in articular joint components such as cartilage, bone and the synovium, attributed to the deletion or overexpression of clock genes in cartilage or chondrocytes. Understanding the functional mechanisms of different genes, the differentiation of mouse phenotypes and the prevention of joint ageing and disease will facilitate future research.

IGF-1 induces cellular senescence in rat articular chondrocytes via Akt pathway activation.

Cellular senescence decreases cell proliferation over time and is characterized by typical markers, including larger cell volume, a flattened morphology, irreversible cell cycle arrest, augmentation of senescence-associated ß-galactosidase (SA-ß-gal) activity and senescence-associated secretory phenotype. A variety of factors are implicated in the process of cellular aging, which mediates an organisms' lifespan. Insulin-like growth factor-1 (IGF-1) serves an essential role in regulating cell growth, division, proliferation and senescence. In the present study, the role of IGF-1 and the downstream Akt signaling pathway in rat articular chondrocyte senescence was assessed. The results of the current study demonstrated that IGF-1 promoted cellular senescence in rat articular chondrocytes via activation of SA-ß-gal and the upregulation of p53 and p21 mRNA and protein levels. IGF-1 enhanced Akt phosphorylation and treatment with Akt inhibitor, MK-2206, significantly suppressed the induction of these markers. Overall, the results indicated the involvement of IGF-1 and Akt in senescence exhibited by rat articular chondrocytes.

The potential role of senescence in limiting fibrosis caused by aging.

Fibrosis-related diseases carry with them a high mortality rate and their morbidity increases with age. Recent findings indicate that induced senescence in myofibroblasts can limit or reduce myocardial fibrosis, cirrhosis, and idiopathic pulmonary fibrosis, while also accelerating wound healing. However, more senescent cells are accumulated as organisms age, which exacerbates aging-related diseases. These two contradictory theories inspired us to summarize papers on the restrictive effect of senescence on fibrosis and to input the key findings into simple software that we developed to assist with data organization and presentation. In this review, we illustrate that senescent cells secrete more matrix metalloproteinases to solubilize excess collagen, while chemokines and cytokines activate immune cells to eliminate senescent cells. In the elderly, it is perhaps more effective to limit fibrosis by inducing myofibroblast senescence and then removing senescent cells that are not cleared via normal mechanisms by antisenescence therapies.

Trash to Treasure: Waste Eggshells as Chemical Reactors for the Synthesis of Amorphous Co(OH)2 Nanorod Arrays on Various Substrates for Applications in Rechargeable Alkaline Batteries and Electrocatalysis.

Bioinspired synthesis has been attracting much attention. Here, we demonstrate a novel approach to directly use waste eggshells as a reactor system for controlled synthesis of nanostructures formed on different substrates. This approach can recycle and transform the "trash" of waste eggshells into "treasure" of unique reactor systems for nanofabrication. The eggshell reactor system can provide unique conditions for the formation of nanostructures on various substrates. Using Co(OH)2 as a model, amorphous Co(OH)2 nanorod arrays, which cannot be synthesized conventionally by direct mixing of precursors, have been successfully formed on various substrates, including Ni foam, metal foil, and glass. To illustrate their potential applications, we use the as-fabricated amorphous Co(OH)2 nanorod arrays on Ni foam as (1) binder-free electrodes for rechargeable alkaline batteries, demonstrating impressively good electrochemical performances, and (2) electrocatalyst for oxygen evolution reaction, demonstrating improved electrocatalytic performances as compared to their crystalline counterpart. We believe the idea outlined here, using eggshell reactor system, can be further expanded to synthesize many different functional materials and precursors which can find additional applications, including self-cleaning, catalysis, sensor, electrochromic devices, etc.

Trash to Treasure: From Harmful Algal Blooms to High-Performance Electrodes for Sodium-Ion Batteries.

Harmful algal blooms (HABs) are frequently reported around the globe. HABs are typically caused by the so-called blue-green algae in eutrophic waters. These fast-growing HABs could be a good source for biomass. Unlike terrestrial plants, they need no land or soil. If HABs could be harvested on a large scale, it could not only possible to mitigate the issue of HABs but also provide a source of biomass. Herein, we demonstrate a facile procedure for converting the HABs into a promising high-performance negative-electrode material for sodium-ion batteries (SIBs). The carbon material derived from blue-green algae demonstrated promising electrochemical performance in reversible sodium storage. The algae used in this work was collected directly from Lake Erie during the algal blooms that affected 500 000 residents in Toledo in 2014. The carbon, derived from the freshly collected HABs by calcination in argon without any additional purification process, delivered a highly stable reversible specific capacity (∼230 mAh/g at a testing current of 20 mA/g) with nearly 100% Columbic efficiency in sodium storage. Impressive rate performance was achieved with a capacity of ∼135 mAh/g even after the testing current was increased fivefold. This proof of concept provides a promising route for mitigating the issue of HABs as "trash" and for generating high-capacity, low-cost electrodes for SIBs as "treasure".

Core-shell Ti@Si coaxial nanorod arrays formed directly on current collectors for lithium-ion batteries.

Silicon is a promising candidate to replace the dominantly used carbon as the anode material for lithium ion batteries (LIBs). Si has the highest theoretical capacity (4200 mA·h/g) and is one of the most abundant elements. Unfortunately, Si has the issues of huge volume variation upon dis/charge cycling and low conductivity, leading to poor cycling and rate performances. Designing special nanostructures and improving conductivity and integration of Si electrodes could dramatically enhance their performance. Here, we introduce a novel strategy to integrate the core-shell nanorod arrays of Ti@Si on Ti foil with good conductivity as an additive-free electrode. The Ti core functions as a stable metallic support for the Si shell and dramatically reduces the diffusion length. The as-prepared core-shell nanorod arrays of Ti@Si on Ti foil, without any postsynthesis treatment, as electrodes demonstrated reversible capacity of 1125 mA·h/g over at least 30 cycles with highly improved Coulombic efficiency.