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Physiology · Digestion

Digestion in the small intestine

Digestio in intestino tenui

Digestion in the small intestine is a key stage of nutrient breakdown, provided by the secretory activity of Lieberkühn glands. The process includes not only the release of liquid juice, but also a unique mechanism of cellular secretion associated with continuous shedding and renewal of the intestinal epithelium.

RenewalComplete replacement of small intestinal epithelial cells occurs on average within 3–6 days.
Medium pHThe mildly alkaline reaction of the intestinal juice is 7.2–7.5 (rising up to 8.6).
EnzymesThe secretion contains over 20 enzymes for breaking down all types of nutrients.
DesquamationAbout 250 grams of destroyed epithelial cells are shed into the intestinal lumen per day.
5 min readFor medical studentsUpdated 09/24/2026
Material prepared by WhiteCoat Pro editorial team based on platform study guidesReviewed by medical editor: Aulov A. A., general practitioner · 09/24/2026

Secretory apparatus and mucosal cells

The secretory function of the small intestine is carried out due to the work of Lieberkühn glands, or intestinal crypts. This complex process involves several specialized types of cellular elements, each performing its own task in ensuring normal food digestion.

  • Goblet cells are responsible for producing complex protective and digestive secretions. Their granular endoplasmic reticulum actively synthesizes protein components, while the Golgi apparatus (lamellar complex) produces mucopolysaccharides. The secretion they release possesses pronounced enzymatic activity, including proteolytic activity.
  • Enterocytes secrete fluid rich in hydrolytic enzymes, which are critically necessary for the final stages of nutrient breakdown.
  • Argentaffin cells, located predominantly deep within the crypts, assume endocrine functions, locally regulating motility and secretory processes.

The intestinal epithelium operates as a complex two-way filter. It not only secretes substances into the intestinal cavity (some of which are preliminarily derived from the bloodstream), but also carries out active and passive transport of digested products from the intestinal lumen and mucosal surface into the circulatory and lymphatic systems.

Physicochemical properties and composition of intestinal juice

Intestinal juice is a complex multicomponent biological fluid. The baseline pH level is 7.2–7.5, but at the peak of secretory activity, when digestion proceeds most intensively, alkalinity can rise to 8.6.

The chemical composition of the juice can be divided into two large groups of substances:

  1. Inorganic components: their concentration is maintained at around 10 g/L. This group includes vital electrolytes — chlorides, bicarbonates, and sodium, potassium, and calcium phosphates.
  2. Organic substances: the liquid fraction contains a large amount of mucus, proteins, amino acids, urea, and various products of cellular metabolism.

The most important organic component of the juice is mucus. It performs a crucial protective function, reliably preventing excessive mechanical damage and aggressive chemical action of acidic chyme on the delicate mucous membrane. In addition, mucus possesses enzymatic function, as it contains high activity of enzymes that hydrolyze nutrients directly near the surface of the wall.

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Morphokinetic secretion

One of the unique physiological features of the small intestine is the so-called morphokinetic (or morphonecrotic) secretion. Essentially, this mechanism represents a continuous cellular conveyor belt that operates throughout a person's life.

The life cycle of an intestinal epithelial cell is strictly programmed and includes three consecutive stages:

  • Continuous formation of new cells deep within the intestinal crypts.
  • Gradual migration of maturing epithelial cells along the body of the villi.
  • Sloughing (desquamation) of aged cells from the tips of the villi into the organ lumen.

The rate of this renewal is colossal. Complete replacement of the entire epithelial layer in an adult occurs on average within 3–6 days (in some cases, 1.4 days). The rate of shedding remains high — about 2% of cells are sloughed off per hour. As a result, about 250 grams of epithelial cells are dumped into the intestinal lumen per day. Breaking down in the lumen, these cells release their contents, becoming a powerful source of enzymes.

Enzymatic profile

The bulk of intestinal juice enzymes are synthesized directly in the mucous membrane of the small intestine, and only an insignificant fraction is excreted in transit from the blood. In total, intestinal juice contains over 20 different hydrolytic enzymes.

Key groups of intestinal juice enzymes:

  • Proteolytic: enterokinase (key activator of pancreatic trypsinogen), specific peptidases (dipeptidase, aminopolypeptidase), and duodenase.
  • Lipolytic: intestinal lipase and phospholipase.
  • Amylolytic and disaccharidases: amylase, lactase, maltase, sucrase, invertase.
  • Others: alkaline phosphatase and nucleases.

An important physiological regularity is the proximodistal gradient. It means that the concentration and functional activity of digestive enzymes are maximal in the initial (proximal) sections of the small intestine and naturally, gradually decrease toward the distal sections and the large intestine.

Briefly: answers to topical questions

What are the mechanisms of neural and humoral regulation of intestinal juice secretion?

Regulation of the functions of the small and large intestines is carried out predominantly through local mechanisms. Local mechanical and chemical irritation increases intestinal activity directly at the site of exposure.

Local mechanical and chemical stimuli act in two ways:

  • via peripheral reflexes;
  • through digestive tract hormones.

Chemical stimulators of nerve endings include acids, alkalis, and food nutrient hydrolysis products.

The humoral pathway consists in the fact that substances enter the blood, are delivered to the glands, and stimulate them directly or indirectly. Gastrointestinal hormones are produced by endocrine cells of the mucosa of the stomach, duodenum, jejunum, and pancreas; their effects include the regulation of water, electrolyte, and enzyme secretion.

According to G.F. Korotko, trigger and correcting mechanisms are distinguished; correcting mechanisms ensure the adaptation of the volume and composition of digestive juices to the quantity and quality of the contents of the stomach and intestines.

What is the precise mechanism of action of enterokinase?

The exact mechanism of action of enterokinase (enteropeptidase) consists in the activation of the inactive enzyme trypsinogen. This process includes the following stages:

  • Cleavage of a hexapeptide from the trypsinogen molecule.
  • Formation of active trypsin.

The activation process proceeds at an optimal pH of 6.8–8.0 and is additionally accelerated in the presence of calcium ions. Subsequently, the formed trypsin causes the subsequent activation of the remaining trypsinogen via autocatalysis.

How to memorize

To memorize the main carbohydrate-splitting enzymes, use the acronym "SALMI": Sucrase, Amylase, Lactase, Maltase, Invertase.

Class and exam questions

Where is the secretion of intestinal juice localized?

The primary site of intestinal secretion production is the Lieberkühn glands (intestinal crypts) located in the mucosa of the small intestine.

What is morphokinetic secretion?

This is a process of continuous epithelial renewal in which cells are formed in the crypts, gradually migrate along the villi, and slough off from their tips, enriching the intestinal juice with enzymes upon their destruction.

What is the essence of the proximodistal gradient?

The proximodistal gradient consists in a regular decrease in the content and activity of digestive enzymes along the course of the small intestine — from its initial sections toward the large intestine.

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What else to study on this topic

  • Mechanisms of neurohumoral regulation of intestinal secretion
  • Parietal (membrane) digestion and the role of the glycocalyx
  • Transport systems for amino acid and monosaccharide absorption
  • The role of bile acids in lipid emulsification and absorption
  • The relationship between villous blood supply and absorption intensity

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