How to Regenerate Beta Cells Naturally

Article written and reviewed by Cyrus Khambatta, PhD
Published February 3, 2021

What Are Beta Cells?

Beta cells are cells in your pancreas that are responsible for the production of insulin, a master hormone that communicates with tissues throughout your body.

Beta cells are insulin-producing cells that are located in clusters of cells called Islets of Langerhans. Beta cells are the only cells in your body capable of producing insulin, which makes your beta cell health critical for normal metabolic function.

Without full beta cell function and normal insulin production, your blood glucose is likely to increase significantly. This lack of functional beta cells is the primary problem in both type 1 diabetes, type 1.5 diabetes, and insulin-dependent type 2 diabetes.

In this article, we’ll explore beta cells, how they can be damaged, and discuss some research being done in the field of beta cell regeneration.

Right now, this work is still in its early stages, but presents a possibility for reversing type 1 and insulin-dependent type 2 diabetes in the future.

Beta Cells And Diabetes

For someone living with any form of diabetes, it is essential to understand how beta cell damage occurs.

For those with type 1 and type 1.5 diabetes, beta cell dysfunction caused by an attack of their own immune system (autoimmunity) is the cause.

For those with prediabetes, type 2 diabetes, and gestational diabetes, beta cell damage does not occur at the initial stages of the disease process.

Beta cell damage only occurs after many months or years of insulin resistance, which then manifests in a “point of no return” where beta cells begin to die resulting mainly from producing excess insulin.

After this point of no return, lifestyle changes are still helpful, but have a reduced effect.

Type 1 Diabetes Beta Cell Regeneration

Type 1 diabetes is caused by a form of biological ‘friendly fire’, in which immune cells mistakenly target beta cells as foreign invaders and destroy them.

This results in an inability of your pancreas to produce insulin, which in turn requires people with type 1 diabetes to inject exogenous (external) insulin in order to manage their blood glucose.

No matter your health or lifestyle, type 1 diabetes is currently incurable, since the human body does not naturally regenerate new beta cells to a clinically relevant extent.

For people with type 1 diabetes, beta cell regeneration is one step towards an eventual cure for this condition, and an area of active scientific research.

Type 2 Diabetes Beta Cell Regeneration

Type 2 diabetes (along with prediabetes and gestational diabetes) is caused by insulin resistance. Insulin resistance results from the accumulation of excess dietary fat in cells that are not meant to store large quantities of fat, which inhibits the action of insulin.

In addition to the symptoms of type 2 diabetes, this accumulation of excess fat in muscle and liver presents a direct threat to beta cells. In an attempt to overcome insulin resistance, beta cells are forced to overproduce insulin, resulting in increased work over many months to years.

Over time, overproduction of insulin strains and eventually kills beta cells.

For people with type 2 diabetes, beta cell death represents a ‘point of no return’, after which they’ll likely require daily, exogenous (external) insulin even if they reverse insulin resistance.

For those with insulin-dependent stage type 2 diabetes, beta cell regeneration would offer a potential opportunity to reverse this ‘point of no return,’ and could lead to a full reversal if implemented alongside lifestyle changes.

What Is Beta Cell Regeneration?

As we mentioned above, there are two ways that beta cells can be damaged or destroyed:

  • Via an autoimmune reaction (which happens in type 1 and type 1.5 diabetes)
  • When beta cells are recruited to produce excess insulin (which happens in late-stage type 2 diabetes)

However, for both of these problems, you face the same hurdle: beta cells are produced almost immediately after birth and do not naturally regenerate, so once they are damaged or destroyed, they’re gone.

Currently, there are ways to successfully manage your health with damaged or destroyed beta cells. Exogenous insulin through a pen, pump, or syringe can supplement for endogenous insulin production to prevent high blood glucose.

Combined with lifestyle changes to become more insulin sensitive — like a plant-based diet, daily exercise, and intermittent fasting — it’s possible to live a long and healthy life after beta cell death.

However, researchers have been searching extensively for ways to stimulate the regrowth of pancreatic beta cells, as a strategy to completely reverse diabetes.

Stimulating the Regeneration of Beta Cells

Restoring beta cells is a complicated task that’s currently being researched from many different research teams around the world.

It’s been theorized that transplantation of beta cells could help, but there are exceptionally few donors, and autoimmune rejection of new cells means that patients often require immunosuppressive drugs for the rest of their life.

As a result, modern research has instead focused on how to regenerate beta cells. It’s a field with many pieces of fascinating research that are in the process of coming together.

The key is understanding what causes beta cells to regenerate, if anything. For example, some studies have attempted to incite other pancreatic islets to propagate into new beta cells, attempting to create beta cells from other nearby cells.

This is a promising area of research, where researchers are isolating the differences of pancreatic cells. In doing so, they hope to find a strategy to produce new beta cells capable of secreting insulin in response to blood glucose.

Another area of promise has come from the use of stem cells, which researchers hope to be able to stimulate to produce new beta cells. However, this area of research is complicated, as the exact way to promote beta cell regeneration remains elusive.

Promise, But Still A Long Way to Go

There are still areas left to explore with this research, but for now, models are limited to in vitro (cellular) results, and some promising trials were done on mice.

In the case of type 1 and type 1.5 diabetes, effective treatment must directly stop the autoimmune process. Because the immune system is what initially attacked the beta cells, any attempt to regenerate beta cells comes secondary to stopping the autoimmune process.

Some research is being done into “reprogramming” the immune system to allow for this beta cell regeneration, but for the moment this is another area with limited success.

To sum up the state of beta cell regeneration in the words of one study, for now, a cure lays out of reach, but promising scientific research could lead to exciting discoveries in the near future.

The Beta Cell Regeneration Diet

It’s important to understand that the search for a dietary approach to regenerate beta cell mass is happening but extremely challenging to investigate.

Promising research from the laboratory of Dr. Valter Longo at the University of Southern California has shown that diabetic mice who were put on the Fasting Mimicking Diet (FMD) underwent a process of “reprogramming” in their pancreatic islet cells, and showed a noticeable increase in insulin production.

Intermittent Fasting and Beta Cell Health

Intermittent fasting — observing strategic daily or weekly periods of calorie restriction — has a strong basis in promoting insulin sensitivity (among many other benefits).

In obese individuals with insulin resistance, intermittent fasting was proven to help preserve beta cell mass, and early research has shown a possible connection between intermittent fasting and production of new beta cells.

Again, these studies are still in the area of promise. There have yet been no conclusive human trials, and the road ahead is still long, but this dietary strategy represents an interesting area of research.

The Good News: You Don’t Have to Wait

Medically induced procedures to spike beta cell regeneration are still in their early phases, just like studies of fasting and a plant-based diet, with further studies and clinical trials needed to confirm these areas of promise.

However, there is one benefit to the dietary approach: you can start it right now, and you’ll experience impressive benefits for your diabetes health and your health overall.

Currently the evidence points to intermittent fasting and a low-fat, plant-based, whole-food diet as the solution to lower your blood glucose, increase your insulin sensitivity, and even reverse type 2 diabetes.

In essence, by following this dietary plan at best you might be protecting your existing beta cell population, while at worst you have a slew of other evidence-based health benefits.

The Final Word

Fortunately, the best plans for reversing diabetes, lowering insulin resistance, having more energy, losing weight, and giving your body the best chance to regenerate insulin cells are all exactly the same.

The blueprint? A low-fat, plant-based, whole-food diet, complemented by daily movement and intermittent fasting. It’s a strategy that’s simple to say, but harder to master.

That’s why we started the Mastering Diabetes Method that you can learn about in this Masterclass. You can take advantage of a vast library of resources and research, work with coaches who are experts in diabetes care, and connect with thousands of other people improving their diabetes health.

Whether you’re working on prevention, helping a family member, or looking to master your own diabetes, we want to help. Let us know how!

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About the author 

Cyrus Khambatta, PhD

Cyrus Khambatta, PhD is a New York Times bestselling co-author of Mastering Diabetes: The Revolutionary Method to Reverse Insulin Resistance Permanently in Type 1, Type 1.5, Type 2, Prediabetes, and Gestational Diabetes. He is the co-founder of Mastering Diabetes and Amla Green, and is an internationally recognized nutrition and fitness coach who has been living with type 1 diabetes since 2002. He co-created the Mastering Diabetes Method to reverse insulin resistance in all forms of diabetes, and has helped more than 10,000 people improve their metabolic health using low-fat, plant-based, whole-food nutrition, intermittent fasting, and exercise. Cyrus earned a Bachelor of Science in Mechanical Engineering from Stanford University in 2003, then earned a PhD in Nutritional Biochemistry from the University of California at Berkeley in 2012. He is the co-author of many peer-reviewed scientific publications. He is the co-host of the annual Mastering Diabetes Online Summit, a featured speaker at the Plant-Based Nutrition and Healthcare Conference (PBNHC), the American College of Lifestyle Medicine Conference (ACLM), Plant Stock, the Torrance Memorial Medical Center, and has been featured on The Doctors, NPR, KQED, Forks Over Knives, Healthline, Fast Company, Diet Fiction, and the wildly popular podcasts the Rich Roll Podcast, Plant Proof, MindBodyGreen, and Nutrition Rounds. Scientific Publications: Sarver, Jordan, Cyrus Khambatta, Robby Barbaro, Bhakti Chavan, and David Drozek. “Retrospective Evaluation of an Online Diabetes Health Coaching Program: A Pilot Study.” American Journal of Lifestyle Medicine, October 15, 2019, 1559827619879106. https://doi.org/10.1177/1559827619879106 Shrivastav, Maneesh, William Gibson, Rajendra Shrivastav, Katie Elzea, Cyrus Khambatta, Rohan Sonawane, Joseph A. Sierra, and Robert Vigersky. “Type 2 Diabetes Management in Primary Care: The Role of Retrospective, Professional Continuous Glucose Monitoring.” Diabetes Spectrum: A Publication of the American Diabetes Association 31, no. 3 (August 2018): 279–87. https://doi.org/10.2337/ds17-0024 Thompson, Airlia C. S., Matthew D. Bruss, John C. Price, Cyrus F. Khambatta, William E. Holmes, Marc Colangelo, Marcy Dalidd, et al. “Reduced in Vivo Hepatic Proteome Replacement Rates but Not Cell Proliferation Rates Predict Maximum Lifespan Extension in Mice.” Aging Cell 15, no. 1 (February 2016): 118–27. https://doi.org/10.1111/acel.12414 Roohk, Donald J., Smita Mascharak, Cyrus Khambatta, Ho Leung, Marc Hellerstein, and Charles Harris. “Dexamethasone-Mediated Changes in Adipose Triacylglycerol Metabolism Are Exaggerated, Not Diminished, in the Absence of a Functional GR Dimerization Domain.” Endocrinology 154, no. 4 (April 2013): 1528–39. https://doi.org/10.1210/en.2011-1047 Price, John C., Cyrus F. Khambatta, Kelvin W. Li, Matthew D. Bruss, Mahalakshmi Shankaran, Marcy Dalidd, Nicholas A. Floreani, et al. “The Effect of Long Term Calorie Restriction on in Vivo Hepatic Proteostatis: A Novel Combination of Dynamic and Quantitative Proteomics.” Molecular & Cellular Proteomics: MCP 11, no. 12 (December 2012): 1801–14. https://doi.org/10.1074/mcp.M112.021204 Bruss, Matthew D., Airlia C. S. Thompson, Ishita Aggarwal, Cyrus F. Khambatta, and Marc K. Hellerstein. “The Effects of Physiological Adaptations to Calorie Restriction on Global Cell Proliferation Rates.” American Journal of Physiology. Endocrinology and Metabolism 300, no. 4 (April 2011): E735-745. https://doi.org/10.1152/ajpendo.00661.2010 Bruss, Matthew D., Cyrus F. Khambatta, Maxwell A. Ruby, Ishita Aggarwal, and Marc K. Hellerstein. “Calorie Restriction Increases Fatty Acid Synthesis and Whole Body Fat Oxidation Rates.” American Journal of Physiology. Endocrinology and Metabolism 298, no. 1 (January 2010): E108-116. https://doi.org/10.1152/ajpendo.00524.2009