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Thorpe, D. W.

Publications and source records attributed to Thorpe, D. W..

3 recordsLinked to original sources

The mood stabilizer lithium alters behaviour and physiology via the gut brain axis.

Lithium, introduced 75 years ago by John Cade1, remains the most effective mood stabilizer for bipolar disorder2. Lithium is proposed to modulate an array of cellular pathways, many ubiquitous to all cells, with pleiotropic roles unlinked to bipolar disorder or lithium responsiveness in genome-wide association studies3,4. These mechanisms cannot explain lithiums specific effects on mood and behaviour. We demonstrate that lithiums primary action is in the periphery, not in the brain itself. Lithium acts in the gut to trigger behavioural and physiological changes, akin to those associated with a torpor-like state, that protect individuals from ingested toxins. Lithium activates gastrointestinal enterochromaffin (EC) cells via their Trpm2 cation channels to modulate afferent vagal and area postrema inputs to the brain. Eliminating these inputs by focal brain lesions eliminates lithiums effects, as does ablation of EC cells or their Trpm2 expression. Lithiums Trpm2-dependent activation of EC cells also occurs in human gut tissue, providing translational relevance for our discovery. These findings challenge the prevailing perception that lithium acts directly on the brain. Via a previously unsuspected gut-brain pathway, lithium engages brain circuitry that reduces arousal and interaction with the external world, therapeutic goals in the manic phase of bipolar disorder.

neuroscience↗

Irinotecan-induced mucositis is associated with variation in the expression of regulatory compounds associated with goblet cells

Alimentary mucositis (AM) is a common side effect of antineoplastic treatment and a key reason for cessation of treatment, compromising the chance of remission. Gastrointestinal mucin secretion is associated with regulatory compounds nitric oxide and its respective synthases inducible, epithelial and neural nitric oxide synthase (iNOS, eNOS and nNOS, respectively), vasoactive intestinal polypeptide (VIP), and prostaglandin E2 (PGE2). Changes in secretion during mucositis have been demonstrated in numerous studies, however no secretory regulatory signals have been associated in mucositis induced secretory change. The aim of this study is to investigate regulator factors in the gastrointestinal tract involved in mucin secretion, VIP, NOS, and PGE2, which are suspected of being involved in mucositis, specifically through alteration of neural or goblet cells. Tumour-bearing Dark Agouti rats received a single dose of 175 mg/kg of irinotecan (i.p.) and 0.01mg/kg atropine. (s.c.). Rats were killed post treatment at 6, 24, 48, 72, 96 and 120 hours. Samples were collected, immunohistochemistry and real time PCR were performed to analyse the expression of iNOS, eNOS, nNOS, VIP, and PGE2. Following irinotecan treatment, staining intensity for iNOS positive goblet cells in the crypts of the jejunum decreased significantly at 48 h (p < 0.05). VIP, and PGE2 positive goblet cell numbers showed no change. mRNA expression in iNOS, eNOS, and nNOS showed no change. Irinotecan-induced mucositis is associated with altered secretory regulatory compounds; this may affect mucin secretion increasing the severity of irinotecan induced mucositis.

pharmacology and toxicology↗

Different liposomal formulations of 5-Fluorouracil result in variations to gastrointestinal toxicities

5-Fluorouracil (5FU) treatment can induce severe mucositis, gastrointestinal toxicity. New formulations of 5-FU increase cancer cytotoxicity, such as neutral liposomes (NL), cationic liposomes (CL), and polyethylenimine copper (PEI-Cu) complexes. However, gastrointestinal toxicity for these new formulations remains unclear. We aim to determine if new formulations in 5FU reduce mucositis by reducing intestinal goblet cell and nerve integrity. Sprague Dawley rats were randomly assigned to groups: saline (n=6), 5FU (n=6 ), NL-5FU (n=5), CL-5FU (n=5), PEI-CU-5FU (n=6), NL-PEI-Cu-5FU (n=5) CL-PEI-Cu-5FU (n=5) (Formulations were equivalent to 10mg/kg 5FU in saline). Treatment was administered daily for 5 days. Rats where humanely killed 2 days after treatment. Haematoxylin and Eosin staining for histological change, Alcian Blue-PAS staining for mucin composition, and immunohistochemistry with S100 antibody for nerve integrity were performed. Statistical analysis using Kruskal-Wallis test with Dunns post-test and Mann Whitney U test d were performed. Effect size was determined using Cohens D test. In the jejunum, inflammatory infiltrate increased in PEI-Cu-5FU rats compared to 5-FU controls (p=0.0011). S100 positive nerve bundles increased in NL-5FU rats compared to saline control (p<0.05). S100 positive cells increased in CL-PEI-Cu-5FU rats compared to saline controls. PEI-Cu-5FU formulation was associated with increased inflammatory infiltrate potentially in response to damage in the jejunum. However, liposomal formulations increased S100 positive neural cells, which may offer protection through increased gastrointestinal motility and contraction. While these formulations of 5FU increase cancer cytotoxicity, the gastrointestinal toxicity remains similar. However, further close monitoring of 5FU formulations for gastrointestinal toxicity is warranted.

molecular biology↗