Human Insulin

Earn CME/CE in your profession:


Continuing Education Activity

The management of type 1 diabetes mellitus entails replacing the actions of the beta cells of the pancreatic islet to detect the need for insulin and to have insulin administered according to the requirements of the patient's body. This activity reviews the indications for the use of insulin, its mechanism of action, routes of administration, contraindications, adverse effects, monitoring its blood concentrations, and toxicity. It also describes in detail how insulin leads to shifts of electrolytes between the intracellular and extracellular compartments. Also, this activity summarizes the cellular production of insulin and its function via its receptor and the numerous effects on carbohydrate, protein, and fat metabolism.

Objectives:

  • Describe the action of insulin on glucose metabolism.
  • Review the synthesis of insulin in pancreatic beta cells.
  • Outline the relationship between insulin and potassium and its importance in the management of patients with diabetic ketoacidosis.
  • Summarize interprofessional team strategies for improving care coordination and communication about the use of insulin to enhance outcomes for patients affected by diabetes mellitus.

Indications

The management of type 1 diabetes mellitus entails replacing the actions of the beta cells of the pancreatic islet to detect the need for insulin and to have insulin administered according to the needs of the patient's body. Insulin is a natural hormone, and it is an essential medication for a multitude of disease states. One of the most critical uses of insulin is in type 1 diabetes mellitus and type 2 diabetes mellitus.[1][2] Insulin is one of the few medications indicated for use in the management of gestational diabetes.[3] Due to its effects of driving potassium into the intracellular compartment, it has utility in managing hyperkalemia.[4] Insulin is a component in the management of complications of diabetes mellitus, including diabetic ketoacidosis as well as the hyperosmolar hyperglycemic state.[5]

There is a proven clinical benefit in using insulin in critical illnesses to prevent or treat hyperglycemia-related toxicity.[6] Commonly, treatment of hypertriglyceridemia includes dietary modifications and medical management with the use of fibrates, fish oil, and niacin, amongst others. One of the other very important applications of insulin is in the treatment of severe hypertriglyceridemia as well as hypertriglyceridemia-induced pancreatitis. Insulin lowers the triglycerides by upregulating the formation of lipoprotein lipase, which works by hydrolyzing the triglycerides. Insulin infusion can help patients with severe hypertriglyceridemia by quickly reducing the blood concentrations of triglycerides to less than 1000 mg/dl.[7]

Mechanism of Action

Insulin’s significant actions focus on storing excess energy in a fed state. Insulin promotes glycogen synthesis, lipid synthesis, protein synthesis, DNA synthesis, and cellular growth and differentiation. Once glucose gets absorbed from a meal, it enters the blood, and then the pancreas releases insulin. Insulin synthesis occurs in the beta cells of the pancreas initially as preproinsulin. Preproinsulin then converts to proinsulin, which then transforms into a single peptide with A, B, and C peptide units. The A and B peptides are joined by disulfide bonds to make insulin and are secreted into the bloodstream. Insulin binds to its cellular receptor. The insulin receptor is composed of alpha subunits, beta subunits, and a tyrosine kinase enzyme. When insulin binds to the alpha subunit, this triggers phosphorylation and activation of the target proteins intracellularly by the tyrosine kinase leading to many effects on cellular metabolism. Activation of the insulin receptor also leads to increased expression of GLUT (a glucose transporter) to the membrane surface and promotes the entry of glucose to the intracellular compartment and then undergoes cellular metabolism. Insulin signals glucose conversion to glycogen for storage and the formation of acetyl coenzyme A and triacylglycerol, which get stored in adipose tissue. Also, insulin directs amino acids for protein synthesis.[3]

In patients with diabetes mellitus, to reach the goal of normal 24-hour insulin activity like in healthy adults without diabetes mellitus, one single insulin formulation with a defined onset, peak, and duration of action is not helpful. Hence there is a need for different kinds of insulin that have different pharmacokinetics. Based on the mode of action, there are four different types of insulin analogs as follows[8]:

Insulin Type Onset Peak activity Duration Notes
Rapid Acting Less than 15 minutes 0.5 to 3 hours 3 to 5 hours
  • Agents include insulin lispro, insulin aspart, and insulin glulisine
  • Onset may vary between products for each patient
  • If mixing with NPH, draw the rapid-acting insulin into the syringe first; give the mixture immediately to avoid effects on peak action
  • Help to achieve post-prandial glycemic control
Short-acting (regular) insulin 0.5 to 1 hour 2 to 4 hours 4 to 8 hours
  • May be mixed with NPH in one syringe. Regular insulin (clear) should be drawn into the syringe first, then the NPH (cloudy) - "clear before cloudy."
  • Administer approximately 30 minutes before meals for the greatest effectiveness.
Intermediate-acting (NPH) insulin 2 to 4 hours 4 to 10 hours 10 to 18 hours
  • Can be administered via a dosing pen or from a vial with a syringe
  • Insulin Lente and insulin Hagedorn are in this category
Long-acting insulin and ultra-long-acting 2 to 3 hours or 4 to 6 hours, depending on the product 6 to 8 hours Up to 24 hours (some products can exceed 24 hours)
  • Cannot be mixed in the same syringe with other insulins
  • Available in pen and vial
  • Duration of action can be dose-dependant
  • Agents include insulin glargine and insulin detemir
70% NPH + 30% regular insulin 0.5 to 1 hour 2 to 10 hours 10 to 18 hours
  • Action has 2 peaks; one from each individual formulation
  • 70% aspart protamine + 30% aspart
  • 75% lispro protamine + 25% lispro
  • 50% lispro protamine + 25% lispro
Less than 15 minutes 1 to 2 hours 10 to 18 hours
  • Action has 2 peaks; one from each individual formulation.

Administration

There are multiple routes of administration of insulin. Insulin is most commonly injected using an insulin syringe. These are plastic disposable syringes available in sizes that hold 30, 50, and 100 units of insulin. They come equipped with a fine gauge needle (up to 31 gauge) with short needle lengths of 3/16 inch for infants up o 1/2 inch or greater for adults. The most frequent administration method is a subcutaneous injection. In rare instances, insulin may be injected into a muscle, but this should only be under close medical supervision, as in a hospital or other facility.

Because of their convenience, insulin pens have gained greater popularity in recent years; these can be disposable or re-usable, the latter utilizing disposable insulin cartridges. Another option is continuous subcutaneous insulin infusion (CSII) devices or insulin pumps. These small computerized devices are programmed to deliver subcutaneous insulin.[9]

Regular insulin and rapid-acting insulins can also be delivered intravenously, but this is only possible under close medical supervision in a clinical setting.[10]

Administration can be as a bolus as an intravenous injection or as a continuous intravenous infusion. Typically, glycemic control is achieved by using basal and prandial insulin administration or by continuous subcutaneous insulin infusion. Recently, the inhalational route for the administration of insulin is available for clinical use.[2][11] Transplantation of the islet cells of the pancreas or pancreatic transplantation is an investigational procedure that can mimic natural insulin synthesis and functionality.[12] Administration of insulin via oral and transdermal routes is being evaluated and may be available shortly for everyday use.[11]

Adverse Effects

As with any other medication, there are clinically significant side effects associated with the use of insulin. Insulin administration can lead to local hypersensitivity reactions such as erythema, pruritus, swelling, and pain at the injection site. Local dermal lipo-dystrophic reactions can occur. An inappropriately excessive dose of insulin or incoordination with meals/missing meals hypoglycemia can occur, which can be life-threatening. Untreated hypoglycemia can cause seizures, coma as well as death, which makes it especially important in elderly patients who are more susceptible. Long-term use of insulin can lead to the production of antibodies against it with the possible development of insulin resistance. As mentioned earlier, insulin can cause the potassium to shift to the intracellular compartment and lead to hypokalemia. Hypokalemia can manifest as cardiac arrhythmias, muscle cramping, gastrointestinal upset, confusion, weakness, and lethargy.[11]

Contraindications

There are a few contraindications to the use of insulin. A patient history of allergic reactions to insulin, its reuse is contraindicated. In patients with insulinoma, where there is excessive endogenous insulin production, the use of exogenous insulin is contraindicated. There is a relative contraindication to using insulin in the setting of hypokalemia. The potassium concentrations must be corrected before administering insulin, as insulin has a known effect of causing hypokalemia.

Monitoring

It is paramount to monitor the blood glucose concentrations while using insulin for optimal glycemic control without causing hypoglycemia (or hyperglycemia). This monitoring is commonly done with regular blood glucose checking with finger prick glucose testing using a glucometer. There are novel techniques now available for continuous glucose monitoring that work via a sensing device inserted subcutaneously. The device measures the glucose concentration in the interstitial fluid between the cells and transmits this information to a monitoring device. The glucose concentrations can be tracked consistently during the day as well as at night with this device. Also, long-term glycemic control can be monitored by using glycated hemoglobin, also known as hemoglobin A1C.

Toxicity

Insulin overdose can cause toxicity by causing hypoglycemia and many additional effects, including arrhythmias, coma, seizures, hypotension, amongst other symptoms. Long-term insulin use may lead to dermal toxicity by causing lipodystrophy. The patient can mitigate this adverse effect by rotating subcutaneous injection sites. Insulin can also cause hypokalemia and related complications, as mentioned earlier in this article.

Enhancing Healthcare Team Outcomes

To enhance patient health outcomes by the healthcare teams, medical education and dissemination of information regarding diabetes mellitus, its complications, and management options are crucial for patient care. All interprofessional healthcare team members (clinicians, pharmacists, nurses) must be mindful of the potential complications as well as how to manage hypoglycemia, hypokalemia, and other complications of insulin pharmacotherapy.

All interprofessional team members should assist in educating the patient and family about the importance of safe insulin dosing. Demonstrations and educational workshops would go a long way toward achieving these goals. It is also crucial to educate the patient to recognize the early signs of hypoglycemia and how to manage diabetes mellitus with insulin and other glycemic control medications. This approach allows the patient to become an integral member of the healthcare team, i.e., its number one focus, and to help in improving overall outcomes by close collaboration. Nursing should ensure proper administration, adherence, and verify monitoring. Pharmacists need to verify dosing, perform medication reconciliation, and instruct patients on administration and how to use their glucose monitor properly. If there are concerns, they should work with the clinician to improve the safe administration of the drug. Monitoring of the blood glucose concentrations, adjusting the dose of insulin as necessary, and lifestyle modifications to prevent chronic complications of diabetes mellitus are significant goals to enhance the patient health outcomes by the healthcare team. [Level 5]


Details

Updated:

8/28/2023 9:45:50 PM

References


[1]

Mathieu C, Gillard P, Benhalima K. Insulin analogues in type 1 diabetes mellitus: getting better all the time. Nature reviews. Endocrinology. 2017 Jul:13(7):385-399. doi: 10.1038/nrendo.2017.39. Epub 2017 Apr 21     [PubMed PMID: 28429780]


[2]

Wallia A, Molitch ME. Insulin therapy for type 2 diabetes mellitus. JAMA. 2014 Jun 11:311(22):2315-25. doi: 10.1001/jama.2014.5951. Epub     [PubMed PMID: 24915263]


[3]

Coustan DR. Gestational diabetes mellitus. Clinical chemistry. 2013 Sep:59(9):1310-21. doi: 10.1373/clinchem.2013.203331. Epub 2013 Mar 27     [PubMed PMID: 23536513]


[4]

Harel Z, Kamel KS. Optimal Dose and Method of Administration of Intravenous Insulin in the Management of Emergency Hyperkalemia: A Systematic Review. PloS one. 2016:11(5):e0154963. doi: 10.1371/journal.pone.0154963. Epub 2016 May 5     [PubMed PMID: 27148740]

Level 1 (high-level) evidence

[5]

Dhatariya KK, Vellanki P. Treatment of Diabetic Ketoacidosis (DKA)/Hyperglycemic Hyperosmolar State (HHS): Novel Advances in the Management of Hyperglycemic Crises (UK Versus USA). Current diabetes reports. 2017 May:17(5):33. doi: 10.1007/s11892-017-0857-4. Epub     [PubMed PMID: 28364357]

Level 3 (low-level) evidence

[6]

Vanhorebeek I, Langouche L, Van den Berghe G. Glycemic and nonglycemic effects of insulin: how do they contribute to a better outcome of critical illness? Current opinion in critical care. 2005 Aug:11(4):304-11     [PubMed PMID: 16015107]

Level 3 (low-level) evidence

[7]

Poonuru S, Pathak SR, Vats HS, Pathak RD. Rapid reduction of severely elevated serum triglycerides with insulin infusion, gemfibrozil and niacin. Clinical medicine & research. 2011 Mar:9(1):38-41. doi: 10.3121/cmr.2010.898. Epub 2010 Sep 17     [PubMed PMID: 20852089]


[8]

Ahmad K. Insulin sources and types: a review of insulin in terms of its mode on diabetes mellitus. Journal of traditional Chinese medicine = Chung i tsa chih ying wen pan. 2014 Apr:34(2):234-7     [PubMed PMID: 24783939]


[9]

Thomas MG, Avari P, Godsland IF, Lett AM, Reddy M, Oliver N. Optimizing type 1 diabetes after multiple daily injections and capillary blood monitoring: Pump or sensor first? A meta-analysis using pooled differences in outcome measures. Diabetes, obesity & metabolism. 2021 Nov:23(11):2521-2528. doi: 10.1111/dom.14498. Epub 2021 Aug 12     [PubMed PMID: 34286892]

Level 1 (high-level) evidence

[10]

Aschner P. Insulin Therapy in Type 2 Diabetes. American journal of therapeutics. 2020 Jan/Feb:27(1):e79-e90. doi: 10.1097/MJT.0000000000001088. Epub     [PubMed PMID: 31567175]


[11]

Matteucci E, Giampietro O, Covolan V, Giustarini D, Fanti P, Rossi R. Insulin administration: present strategies and future directions for a noninvasive (possibly more physiological) delivery. Drug design, development and therapy. 2015:9():3109-18. doi: 10.2147/DDDT.S79322. Epub 2015 Jun 17     [PubMed PMID: 26124635]

Level 3 (low-level) evidence

[12]

Gangemi A, Salehi P, Hatipoglu B, Martellotto J, Barbaro B, Kuechle JB, Qi M, Wang Y, Pallan P, Owens C, Bui J, West D, Kaplan B, Benedetti E, Oberholzer J. Islet transplantation for brittle type 1 diabetes: the UIC protocol. American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons. 2008 Jun:8(6):1250-61. doi: 10.1111/j.1600-6143.2008.02234.x. Epub 2008 Apr 29     [PubMed PMID: 18444920]

Level 2 (mid-level) evidence