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Research

Pancreatitis

Abnormal calcium signalling is a critical feature of pancreatitis:
Pancreatic acinar cells occupy the bulk of the pancreas, making and secreting digestive zymogens into the intestine to break down food for digestion and absorption. Normal signalling within pancreatic acinar cells by calcium causes these cells to secrete inactive enzymes that are activated by duodenal enterokinase, converting trypsinogen to tryspin, which triggers an activation cascade. Excessive cytosolic calcium induces premature digestive enzyme activation within acinar cells, the hallmark of acute pancreatitis. Recurrent attacks lead to the painful, debilitating condition chronic pancreatitis, which in turn confers a markedly increased risk of pancreatic carcinoma. Hereditary pancreatitis successively features all three conditions, caused by trypsinogen gene mutations that make trypsinogen more readily activated, or once activated, more resistant to degradative inactivation. We aim for a full understanding of signalling mechanisms in the pancreas and in other organs, to define the exact cellular triggers and consequences of premature digestive enzyme activation and the course of acute and chronic pancreatitis, as well as to identify and exploit novel therapeutic targets for these major human diseases.
Our discoveries:
We have discovered cytosolic calcium overload to be critical in pancreatitis. Toxins that induce pancreatitis elicit excessive calcium release from intracellular stores, inducing zymogen activation. We have identified alcohol-induced pancreatic injury by fatty acid ethyl esters, non-oxidative ethanol metabolites, which induce calcium overload via inositol trisphosphate receptors so causing mitochondrial injury, necrosis and pancreatitis. We demonstrated direct cholecystokinin stimulation of human pancreatic acinar cells, confirming human and murine parallels, so enhancing drug development. We found excessive pancreatic acinar cell reactive oxygen species promote apoptosis not necrosis, explaining negative clinical trials. We have discovered ed the efficacy of new drugs inhibiting calcium entry via Orai channels as well as drugs inhibiting formation of the mitochondrial permeability transition pore, and using preclinical testing we have demonstrated the importance of door of door to needle time. Phase II trials are currently underway testing calcium entry inhibition in acute pancreatitis. We are leading an open UK-wide phase II trial testing early administration of infliximab in acute pancreatitis, funded by the Efficacy and Mechanism Evaluation Programme (MRC/NIHR): RAPID-I: Randomised treatment of Acute Pancreatitis with Infliximab: Double- blind, placebo-controlled, multi-centre phase II trial.

Pancreatology

My further research includes optimal management of acute pancreatic necrosis; mechanisms of immune destruction of the exocrine pancreas; exocrine and endocrine pancreatic insufficiency and their management; improved selection of patients with chronic pancreatitis for surgery; and development of national and international consensus and guidelines in the optimal management of patients with acute pancreatitis, chronic pancreatitis, pancreatic exocrine insufficiency, pancreatic cancer, gastro-entero-pancreatic neuroendocrine tumours and portal hypertension.

Research grants

Research Capability Funding Open Call

ROYAL LIVERPOOL AND BROADGREEN UNIVERSITY HOSPITALS NHS TRUST (UK)

June 2018 - February 2019

Cypralis Liverpool Research Collaboration in Acute Pancreatitis

INNOVATE UK (UK)

January 2017 - December 2017

Isle of Man Anti-Cancer Association donation to assist with continuing research work at the Liverpool Pancreas Biomedical Research Unit (LPBRU)

ISLE OF MAN ANTI-CANCER ASSOCIATION (ISLE OF MAN)

May 2015 - January 2025

NIHR Senior Investigator Award

DEPARTMENT OF HEALTH & SOCIAL CARE (UK)

April 2016 - March 2024

Liverpool Health Genomics Laboratory

LIVERPOOL HEALTH PARTNERS (UK)

March 2015 - February 2018

The role of intracellular second messengers and premature intracellular enzyme activation in the pathogenesis of acute pancreatitis.

DIGESTIVE DISORDERS FOUNDATION

February 2006 - January 2007

The role of calcium and apoptosis in pancreatic oxidant injury: Intracellular two-photon imaging real time studies.

MEDICAL RESEARCH COUNCIL

March 2004 - August 2007

Role of NF-kappaB signalling in acute experimental pancreatitis

ROYAL LIVERPOOL AND BROADGREEN UNIVERSITY HOSPITALS NHS TRUST (UK)

March 2014 - February 2015

Liverpool Imaging Partnership: Molecular physiology and drug response

MEDICAL RESEARCH COUNCIL

February 2013 - February 2017

Application of high throughput genomic science technologies to NIHR research programmes

ROYAL LIVERPOOL AND BROADGREEN UNIVERSITY HOSPITALS NHS TRUST (UK)

September 2010 - September 2013

Bench fees in support of students within the Pancreas Biomedical Research Unit

WEST CHINA SCHOOL OF MEDICINE SICHUAN UNIVERSITY (CHINA) 🚩

April 2012 - October 2015

Visiting Chinese academic to Pancreas Biomedical Research Unit

CONSULATE GENERAL OF PEOPLE'S REPUBLIC OF CHINA IN MANCHESTER

January 2012 - December 2013

Role of intracellular calcium in the pathogenesis of acute pancreatitis.

MEDICAL RESEARCH COUNCIL

July 2002 - June 2005

Amelie Wareing Research Fellowship for R Mukherjee

DIGESTIVE DISORDERS FOUNDATION

August 2007 - July 2010

An open randomised comparison of the clinical effectiveness and costs of protocol driven opioid analgesia, celiac plexus block, or thoracoscopic splanchnicectomey for pain relief in patients with abdominal malignancy.

DEPARTMENT OF HEALTH & SOCIAL CARE (UK)

February 2001 - January 2004

Cellular biology of the gastrointestinal tract and pancreas in health and disease.

MEDICAL RESEARCH COUNCIL

January 2005 - December 2009

Liver research.

LIVER CANCER APPEAL (UK)

August 2000 - October 2003

Pancreatic acinar cellular mechanisms of injury that determine the severity of acute pancreatitis in rodent, porcine and human pancreas.

ROYAL COLLEGE OF SURGEONS OF ENGLAND(UK)

February 2007 - January 2008

Ca2+ Signalling, Organelle Dysfunction and Pancreatis

MEDICAL RESEARCH COUNCIL

November 2008 - October 2011

Calcium-dependent enzyme activation in acute pancreatitis.

ROYAL LIVERPOOL AND BROADGREEN UNIVERSITY HOSPITALS NHS TRUST (UK)

February 2006 - October 2008

Cyclophilin D Drug Discovery Project

ROYAL LIVERPOOL AND BROADGREEN UNIVERSITY HOSPITALS NHS TRUST (UK)

August 2012 - July 2015

Drug discovery for acute pancreatitis

ROYAL LIVERPOOL AND BROADGREEN UNIVERSITY HOSPITALS NHS TRUST (UK)

April 2012 - March 2013

Interaction of endocytic vacuoles with cellular organelles as a trigger for the cell damage in acute pancreatitis.

MEDICAL RESEARCH COUNCIL

February 2013 - April 2016