Ketogenesis is a catabolic pathway of metabolism. In this process, fatty acids and certain ketogenic amino acids are weakened to derive energy by alternative means. Ketone bodies are produced in the ketogenesis process.
Our body continuously produces ketone bodies in low amounts but in certain cases like starving, when carbohydrates are present in less amount in diet, ketogenesis is preferred to compensate for the energy requirements.
Ketoacidosis is a condition in which an excess amount of ketone bodies gets accumulated in the body. This condition may also be fatal.
Fatty acids undergo 𝛽-oxidation in the liver mitochondria to generate a high amount of energy and form three compounds, that are known as “ketone bodies”. These ketone bodies are water-soluble and do not require lipoproteins for transportation across the membrane. Ketone bodies are lipid molecules having a carbonyl group attached to two -R groups.
The Three Ketone Bodies Formed are:
Our body normally derives energy from stored carbohydrate by the process of glycogenolysis (glycogen → glucose) or from non-carbohydrate sources such as lactate by the process of gluconeogenesis.
Ketogenesis is a process that takes place in a healthy individual continuously, but under certain conditions and they are - when there is increased concentration of fatty acid or carbohydrate reserves are minimized, ketogenesis takes place at a higher rate:
Under low blood glucose level, e.g. during fasting or starvation
On exhaustion of carbohydrate reserve, e.g. glycogen
When there is insufficient insulin, e.g. Type-1 diabetes
All the main body parts such as the brain, skeletal muscles, heart, etc. can utilise the energy formed by ketogenesis.
When there is Insufficient gluconeogenesis in the body, hypoglycemia takes place and excessive production of ketone bodies results in a fatal condition that is called Ketoacidosis.
Liver cell is the main part where the Ketogenesis process occurs primarily. Following are the steps in the process of ketogenesis:
Fatty acids transfer in mitochondria by carnitine palmitoyltransferase CPT-1
𝛽-oxidation of fatty acid to form acetyl CoA
Acetoacetyl-CoA formation: 2 acetyl CoA form acetoacetyl CoA. The reaction is catalyzed by the enzyme thiolase
Synthesis of 3-hydroxy-3-methylglutaryl-CoA (HMG-CoA): the step is catalyzed by HMG-CoA synthase
Acetoacetate formation: HMG-CoA is broken down to acetoacetate and acetyl-CoA by the action of HMG-CoA lyase
Acetoacetate thus produced forms other ketone bodies, acetone by decarboxylation and D-3-hydroxybutyrate by reduction
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Liver produces ketone bodies primarily in the mitochondria but the amazing fact is, it cannot utilise it due to lack of an enzyme 𝛽-keto-acyl-CoA transferase.
Acetoacetate and D-3-hydroxybutyrate are used by the body to get energy. These ketone bodies are circulated out of the liver cell.
In the Extrahepatic Tissues, the following reactions occur:
D-3-hydroxybutyrate is converted back to acetoacetate by 𝛽-hydroxybutyrate dehydrogenase.
Acetoacetate is again brought back to acetyl-CoA by 𝛽-keto-acyl-CoA transferase by converting it.
Acetyl-CoA enters the citric acid cycle (TCA or Kreb’s cycle) and produces 22 ATP molecules.
Acetone is excreted out.
The Ketogenesis process is regulated by Insulin. Hormones such as glucagon, thyroid hormones, catecholamines, cortisol increase the ketogenesis rate by monitoring the breakdown of free fatty acids.
Ketogenesis is employed to ooze out energy by the brain, heart and skeletal muscles under fasting condition
The ketogenic diet (low-carb, fat-rich diet) is used these days to lose weight. The idea is to use the excess fat stored in the body to get energy but excess ketone bodies production can lead to various complications and ketoacidosis
In ketoacidosis condition, the kidneys excrete extra ketone bodies with the water resulting in fluid loss
Ketoacidosis affects the diabetic patients the most because insulin hormone is the main regulator of the process
Symptoms of ketoacidosis include frequent urination, breath smelling like fruits or acetone, nausea, shortness of breath, fatigue, excessive thirst, etc.
Level of ketone bodies present in the body can be tested by blood serum or urine sample analysis
Q1. What is Ketogenesis?
Ans. Ketogenesis is a catabolic pathway of metabolism. In this process, fatty acids and certain ketogenic amino acids are weakened to derive energy by alternative means. Ketone bodies are produced in the ketogenesis process. Our body continuously produces ketone bodies in low amounts but in certain cases like starving, when carbohydrates are present in less amount in diet, ketogenesis is preferred to compensate for the energy requirements. Ketoacidosis is a condition in which an excess amount of ketone bodies gets accumulated in the body. This condition may also be fatal.
Q2. Mention the difference between Ketosis And Ketogenesis?
Ans. Ketosis is the state wherein our body tends to supply ketones at detectable levels, ketogenesis on the opposite hand may be a chemical phenomena which generates those ketones that are produced. Therefore, ketosis is caused as a results of ketogenesis while ketogenesis is initiated from a scarcity of glucose.
Q3. Where does Ketogenesis Occur?
Ans. The process of ketogenesis mainly takes place within the mitochondria of cells of the liver. In this the fatty acids are supplied to mitochondria through carnitine palmitoyltransferase and disintegrated into acetyl CoA via beta-oxidation.