Lunge

Lungene er det viktigaste organet for respirasjon hos luftpustande virveldyr. Den fremste funksjonen er å få oksygen frå jordas atmosfære inn i det kardiovaskulære systemet og få karbondioksid frå blodet til atmosfæra. Dett skjer med millionar av små luftsekkar med tynne veggar og små blodårer på utsida, kor sjølve gassutvekslinga skjer. Lungene har òg funksjonar i tillegg til respirasjonen.

Medisinske omgrep som gjeld lungene startar ofte med pulmo-, frå det latinske pulmonarius ("som gjeld lungene"), eller pleur- gresk pleumon ("lunge").

Respiratory function

Energy production from aerobic respiration often requires oxygen and produces carbon dioxide as a by-product, creating a need for an efficient means of oxygen delivery to cells and carbon dioxide excretion from cells. In smaller organisms, such as single-celled bacteria, this process of gas exchange can take place entirely by simple diffusion. In larger organisms, this is not possible; only a small proportion of cells are close enough to the surface for oxygen from the atmosphere to enter them through diffusion. Two major adaptations made it possible for organisms to attain great multicellularity: an efficient circulatory system that conveyed gases to and from the deepest tissues in the body, and a large, internalised respiratory system that centralized the task of obtaining oxygen from the atmosphere and bringing it into the body, whence it could rapidly be distributed to all tissues via the circulatory system.

In air-breathing vertebrates, respiration occurs in a series of steps. Air is brought into the animal via the airways — in reptiles, birds and mammals this often consists of the nose; the pharynx; the larynx; the trachea; the bronchi and bronchioles; and the terminal branches of the respiratory tree. The lungs of mammals are a rich lattice of alveoli, which provide an enormous surface area for gas exchange. A network of fine capillaries allows transport of blood over the surface of alveoli. Oxygen from the air inside the alveoli diffuses into the bloodstream, and carbon dioxide diffuses from the blood to the alveoli, both across the exceptionally thin alveolar membranes. The drawing and expulsion of air is driven by muscular action; in early tetrapods, air was driven into the lungs by the pharyngeal muscles, whereas in reptiles, birds and mammals a more complicated musculoskeletal system is used. In the mammal, a large muscle, the diaphragm (in addition to the internal intercostal muscles), drive ventilation by periodically altering the intra-thoracic volume and pressure; by increasing volume and thus decreasing pressure, air flows into the airways down a pressure gradient, and by reducing volume and increasing pressure, the reverse occurs. During normal breathing, expiration is passive and no muscles are contracted (the diaphragm relaxes).

Nonrespiratory functions

In addition to respiratory functions such as gas exchange and regulation of hydrogen ion concentration, the lungs also:

influence the concentration of biologically active substances and drugs used in medicine in arterial blood
filter out small blood clots formed in veins
serve as a physical layer of soft, shock-absorbent protection for the heart, which the lungs flank and nearly enclose.

Mammalian lungs

The lungs of mammals have a spongy texture and are honeycombed with epithelium having a much larger surface area in total than the outer surface area of the lung itself. The lungs of humans are typical of this type of lung. The environment of the lung is very moist, which makes it a hospitable environment for bacteria. Many respiratory illnesses are the result of bacterial or viral infection of the lungs.

Breathing is largely driven by the muscular diaphragm at the bottom of the thorax. Contraction of the diaphragm vertically expands the cavity in which the lung is enclosed. Relaxation of the diaphragm has the opposite effect. The rib cage itself is also able to expand and contract to some degree, through the action of other respiratory and accessory resipratory muscles. As a result, air is sucked into or expelled out of the lungs, always moving down its pressure gradient.

Air enters through the oral and nasal cavities; it flows through the larynx and into the trachea, which branches out into bronchi. In humans, it is the two main bronchi (produced by the bifurcation of the trachea) that enter the roots of the lungs. The bronchi continue to divide within the lung, and after multiple generations of divisions, give rise to bronchioles. Eventually the bronchial tree ends in alveolar sacs, composed of alveoli. Aveoli are essentially tiny sacs in close contact with blood filled capillaries. Here oxygen from the air diffuses into the blood, where it is carried by hemoglobin, and carried via pulmonary veins towards the heart.

Deoxygenated blood from the heart travels via pulmonary arteryto the lungs, for oxidation.

Anatomy

The lungs are located inside the thoracic cavity, protected by the bony structure of the rib cage. Each is enclosed by a double-layered sac called pleura. The inner layer of the sac (visceral pleura) adheres tightly to the lung and the outer layer (parietal pleura) is attached to the inner wall of the thoracic cavity. The two layers are separated by a thin space called the pleural cavity that is filled with pleural fluid; this allows the inner and outer layers to slide over each other, and prevents them from being separated easily. The left lung is smaller than the right one, to provide room for the heart.

The lungs attach to the heart and trachea through structures that are called the "roots of the lungs." The roots of the lungs are the bronchi, pulmonary vessels, bronchial vessels, lymphatic vessels, and nerves. These structures enter and leave at the hilus of the lung.

The lungs are divided into lobes by the horizontal and oblique fissures. The right lung has three lobes and the left lung has two. A unique feature of the left lung is the cardiac notch, which helps create the lingula (Latin for "tongue") of the left lung.

The lungs are connected to the upper airway by the trachea and bronchi. The trachea runs down the neck and divides into left and right bronchi behind the sternal angle ( at the level of the fourth thoracic vertebra T4). The right main bronchus is shorter, wider and runs more vertically than the left. For this reason, it is more common to aspirate foreign objects into the right lung.

The right bronchus gives rise to the superior lobe bronchus before entering the hilum and dividing into the middle and inferior lobe bronchus. The left bronchus enters the hilum and gives rise to the superior and inferior lobe bronchi.

The bronchi enter the lung and branch out to form the bronchial tree. The bronchi divide into smaller bronchioles, which terminate into alveoli. An alveolus is composed of respiratory tissue and is the site of gas exchange in the lung. The inner walls of the alveoli are covered in surfactant, a fluid which reduces the surface tension of the alveoli, allowing them to expand and recoil with inspiration and expiration and preventing them from collapsing.

The blood supply to the lungs is from two sources: the pulmonary vessels and the bronchial vessels. The bronchial vessels support the nonrespiratory tissue and the pulmonary vessels provide support to the respiratory tissue.

The pulmonary arteries carry deoxygenated blood, which has returned to the heart from the systemic venous system, to the lungs to be reoxygenated. The pulmonary veins carry oxygenated blood back to the heart to go to the systemic arterial system. The right and left pulmonary arteries arise from the pulmonary trunk and carry deoxygenated blood to their respective lungs. The pulmonary veins, two on each side, carry oxygenated blood to the left atrium of the heart.

The bronchial arteries that supply the nonrespiratory tissue of the lung arise from different sources. The left bronchial arteries come off of the thoracic aorta, however, the right bronchial artery has a variable source.

Avian lungs

Birds have a complex but highly efficient crosscurrent exchange system in their lungs, accompanied by air sacs to control the flow of gas through it. See bird respiration for a detailed account of this system.

The lungs of birds differ significantly from those of mammals. In addition to the lungs themselves, birds have posterior and anterior air sacs (typically nine) which control air flow through the lungs, but do not play a direct role in gas exchange. They have a flow-through respiration system.

When a bird inhales, air flows in through the trachea to the posterior air sacs, while air currently within the lungs flows into the anterior air sacs. When the bird exhales, the fresh air now contained within the posterior air sacs is driven into the lungs, and the stale air now contained within the anterior air sacs is expelled through the trachea and into the atmosphere. Two complete cycles of inhalation and exhalation are, therefore, required for one breath of air to make its way through the avian respiratory system.

Avian lungs do not have alveoli, as mammalian lungs do, but instead contain millions of tiny passages known as parabronchi, connected at either ends by the dorsobronchi and ventrobronchi. Air flows through the honeycombed walls of the parabronchi and into air capillaries, where oxygen and carbon dioxide are traded with cross-flowing blood capillaries by diffusion, a process of crosscurrent exchange.

The purpose of this complex system of air sacs is to ensure that the airflow through the avian lung is always traveling in the same direction - posterior to anterior. This is in contrast to the mammalian system, in which the direction of airflow in the lung is tidal, reversing between inhalation and exhalation. By utilizing a unidirectional flow of air, avian lungs are able to extract a greater concentration of oxygen from inhaled air. Birds are thus equipped to fly at altitudes at which mammals would succumb to hypoxia.

Reptilian lungs

Reptilian lungs are typically ventilated by a combination of expansion and contraction of the ribs via axial muscles and buccal pumping. Crocodilians also rely on the hepatic piston method, in which the liver is pulled back by a muscle anchored to the pubic bone (part of the pelvis), which in turn pulls the bottom of the lungs backward, expanding them.

Amphibian lungs

The lungs of most frogs and other amphibians are simple balloon-like structures, with gas exchange limited to the outer surface area of the lung. This is not a very efficient arrangement, but amphibians have low metabolic demands and also frequently supplement their oxygen supply by diffusion across the moist outer skin of their bodies.

Arachnid lungs

Spiders have structures called "book lungs", which are not evolutionarily related to vertebrate lungs but serve a similar respiratory purpose.

Crustacean lungs

The Coconut crab uses structures called branchiostegal lungs to breathe air, and indeed will drown in water.

Origins

The first lungs, simple sacs that allowed the organism to gulp air under oxygen-poor conditions, evolved into the lungs of today's terrestrial vertebrates and into the gas bladders of today's fish. The lungs of vertebrates are homologous to the gas bladders of fish (but not to their gills). The evolutionary origin of both are thought to be outpocketings of the upper intestines. This is reflected by the fact that the lungs of a fetus also develop from an outpocketing of the upper intestines and in the case of gas bladders, this connection to the gut continues to exist as the pneumatic duct in more "primitive" teleosts, and is lost in the higher orders. (This is an instance of correlation between ontogeny and phylogeny.) There are no animals which have both lungs and a gas bladder.

External links

respirasjonssystemet | pulmologi

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