The scientific community has been in a heated debate about xenotransplants (transplanting pig islets into humans). Although the procedures are showing to be effective - is the insulin secretion entirely pig? Some experts surmise that after the transplants, diabetic patients are actually able to produce some insulin on their own, after all.

The latest press release from Tissera, Inc (an Israeli-based company) made a statement that raises my hopes. It was, "By the fourth month after transplantation, the insulin dose needed to maintain near-normal blood sugar levels decreased by more than 90% in comparison with the insulin dose needed before transplantation, meaning that endogenous insulin production was predominantly responsible for blood sugar control."

The question of the origin of endogenous insulin was addressed by measurement of blood C-peptide. C-peptide splits from insulin and indicates the level of insulin secretion from the patient. C-peptide levels were measured both at baseline and in response to a sugar load, which brings about a rise in blood C-peptide. The measured C-peptide was shown to be predominantly of pig origin. So herein lies my question: is predominantly more than 50%? A type 1 diabetic has undetectable levels of C-peptide. Period. After the xenotransplant the C-peptide level is all of a sudden detectable? Could these islet transplants assist in regenerating the diabetics' own islets?

The Edmonton Protocol has been temporarily put on hold due to fears the human form of mad cow disease might infect patients.

The source of an enzyme used in transplants was reported to derive from cow brains. Transplants of these treated islets have been put on hold until a source for this enzyme can be found that doesn't use cow brains. Dr. James Shapiro, the surgeon who developed the Edmontol Protocol said, "we just decided to put the program on hold". Shapiro and his team transplant healthy islet cells into the pancreas of people with Type 1 diabetes. The healthy cells allow recipients to again begin producing insulin crucial to the body's ability to regulate sugar digestion.

The National Institutes of Health was creating a similar program in the United States when it discovered that one of the biomedical compounds that Shapiro's team has been using depends on cow brains. Roche Applied Sciences was selling the team an enzyme that allows doctors to extract healthy islet cells. But Roche was buying the bacteria that secretes the enzyme from a third company, which grew the bacteria using fat from cow brains. Roche spokeswoman Michele Beaubien said from Montreal that the enzyme is sold for research purposes only.

The more I learn these days about medicine and how it is applied to diabetes - the more I feel as though everything is for research purposes only. Don't you? As Yogi Berra said, "it ain't over till it's over". A big thanks to Dave of No Sugar Tonight for bringing this story to my attention.