Alzheimer’s disease (AD) represents a major global health challenge, characterised by progressive neurodegeneration that leads to cognitive decline. Inflammation is a key factor in the pathogenesis of AD, affecting both neuroinflammation and systemic inflammation. In AD, neuroinflammation is marked by the activation of microglia and the release of pro-inflammatory cytokines, which exacerbate neuronal damage and cognitive deficits. Systemic inflammation further compromises the blood–brain barrier (BBB), increasing its permeability and permitting the entry of inflammatory molecules and immune cells into the brain, thereby advancing the disease’s hallmark features. Recent studies have elucidated the influence of gut microbiota dysbiosis on AD and inflammation. This imbalance is thought to be associated with alterations in the concentrations of short-chain fatty acids (SCFAs) and bile acids, which can modulate neuroinflammation and contribute to AD pathology. Additionally, imbalances in neurotransmitters resulting from gut microbiota dysbiosis can further disrupt brain function and facilitate AD progression. This review provides an overview of the hypothesis that systemic and central nervous system (CNS) inflammation, together with gut-microbiota dysbiosis, may interact to influence the development and progression of AD.

Hypophosphatemic rickets (HR) is a syndrome of hypophosphatemia and rickets that resembles vitamin D deficiency, which is caused by malfunction of renal tubules in phosphate reabsorption. Phosphate is an essential mineral, which is important for bone and tooth structure. It is regulated by parathyroid hormone, 1,25-dihydroxyvitamin D and fibroblast-growth-factor 23 (FGF23). X-linked hypophosphatemia (XLH), autosomal dominant HR (ADHR), and autosomal recessive HR (ARHR) are examples of hereditary forms of HR, which are mainly caused by mutations in the phosphate regulating endopeptidase homolog, X-linked (PHEX), FGF23, and, dentin matrix protein-1 (DMP1) and ecto-nucleotide pyro phosphatase/phosphodiesterase 1 (ENPP1) genes, respectively. Mutations in these genes are believed to cause elevation of circulating FGF23 protein. Increase in FGF23 disrupts phosphate homeostasis, leading to HR. This review aims to summarize phosphate homeostasis and focuses on the genes and mutations related to XLH, ADHR, and ARHR. A compilation of XLH mutation hotspots based on the PHEX gene database and mutations found in the FGF23, DMP1, and ENPP1 genes are also made available in this review.

Chronic relapsing inflammatory bowel disease is strongly linked to an increased risk of colitis-associated cancer (CAC). One of the well-known inflammatory carcinogenesis pathways, phosphatidylinositol 3-kinase (PI3K), was identified to be a crucial mechanism in long-standing ulcerative colitis (UC). The goal of this study was to identify somatic variants in the cytokine-induced PI3K-related genes in UC, colorectal cancer (CRC) and CAC. Thirty biopsies (n = 8 long-standing UC, n = 11 CRC, n = 8 paired normal colorectal mucosa and n = 3 CAC) were subjected to targeted sequencing on 13 PI3K-related genes using Illumina sequencing and the SureSelectXT Target Enrichment System. The Genome Analysis Toolkit was used to analyze variants, while ANNOVAR was employed to detect annotations. There were 5116 intronic, 355 exonic, 172 untranslated region (UTR) and 59 noncoding intronic variations detected across all samples. Apart from a very small number of frameshifts, the distribution of missense and synonymous variants was almost equal. We discovered changed levels of IL23R, IL12Rß1, IL12Rß2, TYK2, JAK2 and OSMR in more than 50% of the samples. The IL23R variant in the UTR region, rs10889677, was identified to be a possible variant that might potentially connect CAC with UC and CRC. Additional secondary structure prediction using RNAfold revealed that mutant structures were more unstable than wildtype structures. Further functional research on the potential variants is, therefore, highly recommended since it may provide insight on the relationship between inflammation and cancer risk in the cytokine-induced PI3K pathway.

Polychaetes possess the ability to regenerate anterior and posterior segments following injury or self-amputation, offering a tractable system for studying wound repair and tissue patterning. To support comparative and mechanistic studies in annelid regeneration, this study presents a protocol for inducing and characterizing anterior regeneration in Diopatra claparedii (D. claparedii). The protocol outlines steps for specimen handling, immobilisation, and precise amputation, followed by scheduled observational time points to document morphological progression throughout regeneration. D. claparedii were gently removed from their tubes using a blunt-ended stick and immobilised in 4% magnesium chloride to induce relaxation. Anterior amputation was performed at the 4th chaetiger under a stereomicroscope, and the regeneration process was monitored on days 1, 6, 15, 30, and 60 post-amputation. The procedure enables consistent induction of anterior regeneration and captures key morphological features across early wound closure, blastema formation, and segment re-establishment. By providing a reproducible workflow and morphological reference for D. claparedii, this protocol offers a practical foundation that supports future investigations that aim to relate morphological observations to underlying cellular or molecular processes in annelid regeneration.

Polychaetes possess the ability to regenerate anterior and posterior segments following injury or self-amputation, offering a tractable system for studying wound repair and tissue patterning. To support comparative and mechanistic studies in annelid regeneration, this study presents a protocol for inducing and characterizing anterior regeneration in Diopatra claparedii (D. claparedii). The protocol outlines steps for specimen handling, immobilisation, and precise amputation, followed by scheduled observational time points to document morphological progression throughout regeneration. D. claparedii were gently removed from their tubes using a blunt-ended stick and immobilised in 4% magnesium chloride to induce relaxation. Anterior amputation was performed at the 4th chaetiger under a stereomicroscope, and the regeneration process was monitored on days 1, 6, 15, 30, and 60 post-amputation. The procedure enables consistent induction of anterior regeneration and captures key morphological features across early wound closure, blastema formation, and segment re-establishment. By providing a reproducible workflow and morphological reference for D. claparedii, this protocol offers a practical foundation that supports future investigations that aim to relate morphological observations to underlying cellular or molecular processes in annelid regeneration.