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Function of the autotransplanted pancreatic segment in the dog
The Journal of Cardiovascular Surgery
|January 1, 1978
Summary
Pancreatic autotransplantation in dogs showed that while grafts initially responded to secretin, severe autolysis occurred in most cases. Cellular damage and enzyme leakage were key factors in graft failure.
Area of Science:
- Surgical transplantation
- Gastroenterology
- Pancreatic physiology
Background:
- Autotransplantation of pancreatic tissue is a complex surgical procedure.
- Assessing immediate graft function post-transplantation is crucial for understanding viability.
- Limited data exists on the long-term viability and autolysis patterns of pancreatic grafts.
Purpose of the Study:
- To evaluate the functional capacity of autotransplanted pancreatic grafts in dogs.
- To investigate the role of cellular damage and enzyme leakage in graft autolysis.
- To examine pancreatic secretion and enzyme levels immediately following transplantation.
Main Methods:
- Autotransplantation of the left pancreatic lobe into neck vessels in 13 dogs.
- Functional examination of pancreatic secretion and arteriovenous enzyme differences.
- Postoperative monitoring for graft integrity and signs of autolysis.
- Stimulation with secretin to assess exocrine function.
Main Results:
- Grafts were intact in only 3 of 13 dogs by postoperative day 20.
- Severe autolysis of the graft and surrounding tissues occurred in 10 dogs within 4-6 days.
- Secretin stimulation elicited immediate graft secretion with normal amylase output.
- Significant arteriovenous differences for amylase and LDH were observed.
- Enzyme levels in graft vasculature increased markedly after exocrine stimulation.
Conclusions:
- Pancreatic autotransplantation in dogs is prone to rapid autolysis.
- Cellular damage and subsequent enzyme leakage are significant contributors to graft failure.
- Despite autolysis, remaining functional pancreatic tissue can respond to secretin stimulation.