The lungs are located within the thoracic cavity and are surrounded by the pleural membranes. Each lung has a conical shape with an apex and base. The right lung is divided into three lobes and the left lung into two lobes by fissures. Over 300 million alveoli within the lungs provide a vast surface area for gas exchange to occur between the air in the alveoli and blood in the pulmonary capillaries.
Ventilation and Perfusion in different zones of lungs.Gyaltsen Gurung
This powerpoint presentation will make you explore about the Perfusion and Ventilation in different zones of lungs with its co-relation with pulmonary tuberculosis.
Ventilation and Perfusion in different zones of lungs.Gyaltsen Gurung
This powerpoint presentation will make you explore about the Perfusion and Ventilation in different zones of lungs with its co-relation with pulmonary tuberculosis.
Gas exchange between the alveoli and the pulmonary capillary blood occurs by diffusion, as will be discussed in the next chapter. Diffusion of oxygen and carbon dioxide occurs passively, according to their concentration differences across the alveolar-capillary barrier. These concentration differences must be maintained by ventilation of the alveoli and perfusion of the pulmonary capillaries.
Alveolar ventilation brings oxygen into the lung and removes carbon dioxide from it. Similarly, the mixed venous blood brings carbon dioxide into the lung and takes up alveolar oxygen. The alveolar Image not available. and Image not available. are thus determined by the relationship between alveolar ventilation and pulmonary capillary perfusion. Alterations in the ratio of ventilation to perfusion, called the Image not available., will result in changes in the alveolar Image not available. and Image not available., as well as in gas delivery to or removal from the lung.
Alveolar ventilation is normally about 4 to 6 L/min and pulmonary blood flow (which is equal to cardiac output) has a similar range, and so the Image not available. for the whole lung is in the range of 0.8 to 1.2. Image not available. However, ventilation and perfusion must be matched on the alveolar-capillary level, and the Image not available. for the whole lung is really of interest only as an approximation of the situation in all the alveolar-capillary units of the lung. For instance, suppose that all 5 L/min of the cardiac output went to the left lung and all 5 L/min of alveolar ventilation went to the right lung. The whole lung Image not available. would be 1.0, but there would be no gas exchange because there could be no gas diffusion between the ventilated alveoli and the perfused pulmonary capillaries.
Oxygen is delivered to the alveolus by alveolar ventilation, is removed from the alveolus as it diffuses into the pulmonary capillary blood, and is carried away by blood flow. Similarly, carbon dioxide is delivered to the alveolus in the mixed venous blood and diffuses into the alveolus in the pulmonary capillary. The carbon dioxide is removed from the alveolus by alveolar ventilation. As will be discussed in Chapter 6, at resting cardiac outputs the diffusion of both oxygen and carbon dioxide is normally limited by pulmonary perfusion. Thus, the alveolar partial pressures of both oxygen and carbon dioxide are determined by the Image not available. If the Image not available. in an alveolar-capillary unit increases, the delivery of oxygen relative to its removal will increase, as will the removal ...
Slideshow is from the University of Michigan Medical School's M1 Cardiovascular / Respiratory sequence
View additional course materials on Open.Michigan:
openmi.ch/med-M1Cardio
Gas exchange between the alveoli and the pulmonary capillary blood occurs by diffusion, as will be discussed in the next chapter. Diffusion of oxygen and carbon dioxide occurs passively, according to their concentration differences across the alveolar-capillary barrier. These concentration differences must be maintained by ventilation of the alveoli and perfusion of the pulmonary capillaries.
Alveolar ventilation brings oxygen into the lung and removes carbon dioxide from it. Similarly, the mixed venous blood brings carbon dioxide into the lung and takes up alveolar oxygen. The alveolar Image not available. and Image not available. are thus determined by the relationship between alveolar ventilation and pulmonary capillary perfusion. Alterations in the ratio of ventilation to perfusion, called the Image not available., will result in changes in the alveolar Image not available. and Image not available., as well as in gas delivery to or removal from the lung.
Alveolar ventilation is normally about 4 to 6 L/min and pulmonary blood flow (which is equal to cardiac output) has a similar range, and so the Image not available. for the whole lung is in the range of 0.8 to 1.2. Image not available. However, ventilation and perfusion must be matched on the alveolar-capillary level, and the Image not available. for the whole lung is really of interest only as an approximation of the situation in all the alveolar-capillary units of the lung. For instance, suppose that all 5 L/min of the cardiac output went to the left lung and all 5 L/min of alveolar ventilation went to the right lung. The whole lung Image not available. would be 1.0, but there would be no gas exchange because there could be no gas diffusion between the ventilated alveoli and the perfused pulmonary capillaries.
Oxygen is delivered to the alveolus by alveolar ventilation, is removed from the alveolus as it diffuses into the pulmonary capillary blood, and is carried away by blood flow. Similarly, carbon dioxide is delivered to the alveolus in the mixed venous blood and diffuses into the alveolus in the pulmonary capillary. The carbon dioxide is removed from the alveolus by alveolar ventilation. As will be discussed in Chapter 6, at resting cardiac outputs the diffusion of both oxygen and carbon dioxide is normally limited by pulmonary perfusion. Thus, the alveolar partial pressures of both oxygen and carbon dioxide are determined by the Image not available. If the Image not available. in an alveolar-capillary unit increases, the delivery of oxygen relative to its removal will increase, as will the removal ...
Slideshow is from the University of Michigan Medical School's M1 Cardiovascular / Respiratory sequence
View additional course materials on Open.Michigan:
openmi.ch/med-M1Cardio
The above Presentation is related to the Lungs Histology for 1st year MBBS student. it covers the trachea, lungs, bronchi upto the level of Alveoli. Also, it will help students to learn that what different type of epithelium are present at which region.
These simplified slides by Dr. Sidra Arshad present an overview of the non-respiratory functions of the respiratory tract.
Learning objectives:
1. Enlist the non-respiratory functions of the respiratory tract
2. Briefly explain how these functions are carried out
3. Discuss the significance of dead space
4. Differentiate between minute ventilation and alveolar ventilation
5. Describe the cough and sneeze reflexes
Study Resources:
1. Chapter 39, Guyton and Hall Textbook of Medical Physiology, 14th edition
2. Chapter 34, Ganong’s Review of Medical Physiology, 26th edition
3. Chapter 17, Human Physiology by Lauralee Sherwood, 9th edition
4. Non-respiratory functions of the lungs https://academic.oup.com/bjaed/article/13/3/98/278874
micro teaching on communication m.sc nursing.pdfAnurag Sharma
Microteaching is a unique model of practice teaching. It is a viable instrument for the. desired change in the teaching behavior or the behavior potential which, in specified types of real. classroom situations, tends to facilitate the achievement of specified types of objectives.
CDSCO and Phamacovigilance {Regulatory body in India}NEHA GUPTA
The Central Drugs Standard Control Organization (CDSCO) is India's national regulatory body for pharmaceuticals and medical devices. Operating under the Directorate General of Health Services, Ministry of Health & Family Welfare, Government of India, the CDSCO is responsible for approving new drugs, conducting clinical trials, setting standards for drugs, controlling the quality of imported drugs, and coordinating the activities of State Drug Control Organizations by providing expert advice.
Pharmacovigilance, on the other hand, is the science and activities related to the detection, assessment, understanding, and prevention of adverse effects or any other drug-related problems. The primary aim of pharmacovigilance is to ensure the safety and efficacy of medicines, thereby protecting public health.
In India, pharmacovigilance activities are monitored by the Pharmacovigilance Programme of India (PvPI), which works closely with CDSCO to collect, analyze, and act upon data regarding adverse drug reactions (ADRs). Together, they play a critical role in ensuring that the benefits of drugs outweigh their risks, maintaining high standards of patient safety, and promoting the rational use of medicines.
Recomendações da OMS sobre cuidados maternos e neonatais para uma experiência pós-natal positiva.
Em consonância com os ODS – Objetivos do Desenvolvimento Sustentável e a Estratégia Global para a Saúde das Mulheres, Crianças e Adolescentes, e aplicando uma abordagem baseada nos direitos humanos, os esforços de cuidados pós-natais devem expandir-se para além da cobertura e da simples sobrevivência, de modo a incluir cuidados de qualidade.
Estas diretrizes visam melhorar a qualidade dos cuidados pós-natais essenciais e de rotina prestados às mulheres e aos recém-nascidos, com o objetivo final de melhorar a saúde e o bem-estar materno e neonatal.
Uma “experiência pós-natal positiva” é um resultado importante para todas as mulheres que dão à luz e para os seus recém-nascidos, estabelecendo as bases para a melhoria da saúde e do bem-estar a curto e longo prazo. Uma experiência pós-natal positiva é definida como aquela em que as mulheres, pessoas que gestam, os recém-nascidos, os casais, os pais, os cuidadores e as famílias recebem informação consistente, garantia e apoio de profissionais de saúde motivados; e onde um sistema de saúde flexível e com recursos reconheça as necessidades das mulheres e dos bebês e respeite o seu contexto cultural.
Estas diretrizes consolidadas apresentam algumas recomendações novas e já bem fundamentadas sobre cuidados pós-natais de rotina para mulheres e neonatos que recebem cuidados no pós-parto em unidades de saúde ou na comunidade, independentemente dos recursos disponíveis.
É fornecido um conjunto abrangente de recomendações para cuidados durante o período puerperal, com ênfase nos cuidados essenciais que todas as mulheres e recém-nascidos devem receber, e com a devida atenção à qualidade dos cuidados; isto é, a entrega e a experiência do cuidado recebido. Estas diretrizes atualizam e ampliam as recomendações da OMS de 2014 sobre cuidados pós-natais da mãe e do recém-nascido e complementam as atuais diretrizes da OMS sobre a gestão de complicações pós-natais.
O estabelecimento da amamentação e o manejo das principais intercorrências é contemplada.
Recomendamos muito.
Vamos discutir essas recomendações no nosso curso de pós-graduação em Aleitamento no Instituto Ciclos.
Esta publicação só está disponível em inglês até o momento.
Prof. Marcus Renato de Carvalho
www.agostodourado.com
The Gram stain is a fundamental technique in microbiology used to classify bacteria based on their cell wall structure. It provides a quick and simple method to distinguish between Gram-positive and Gram-negative bacteria, which have different susceptibilities to antibiotics
Explore natural remedies for syphilis treatment in Singapore. Discover alternative therapies, herbal remedies, and lifestyle changes that may complement conventional treatments. Learn about holistic approaches to managing syphilis symptoms and supporting overall health.
Title: Sense of Taste
Presenter: Dr. Faiza, Assistant Professor of Physiology
Qualifications:
MBBS (Best Graduate, AIMC Lahore)
FCPS Physiology
ICMT, CHPE, DHPE (STMU)
MPH (GC University, Faisalabad)
MBA (Virtual University of Pakistan)
Learning Objectives:
Describe the structure and function of taste buds.
Describe the relationship between the taste threshold and taste index of common substances.
Explain the chemical basis and signal transduction of taste perception for each type of primary taste sensation.
Recognize different abnormalities of taste perception and their causes.
Key Topics:
Significance of Taste Sensation:
Differentiation between pleasant and harmful food
Influence on behavior
Selection of food based on metabolic needs
Receptors of Taste:
Taste buds on the tongue
Influence of sense of smell, texture of food, and pain stimulation (e.g., by pepper)
Primary and Secondary Taste Sensations:
Primary taste sensations: Sweet, Sour, Salty, Bitter, Umami
Chemical basis and signal transduction mechanisms for each taste
Taste Threshold and Index:
Taste threshold values for Sweet (sucrose), Salty (NaCl), Sour (HCl), and Bitter (Quinine)
Taste index relationship: Inversely proportional to taste threshold
Taste Blindness:
Inability to taste certain substances, particularly thiourea compounds
Example: Phenylthiocarbamide
Structure and Function of Taste Buds:
Composition: Epithelial cells, Sustentacular/Supporting cells, Taste cells, Basal cells
Features: Taste pores, Taste hairs/microvilli, and Taste nerve fibers
Location of Taste Buds:
Found in papillae of the tongue (Fungiform, Circumvallate, Foliate)
Also present on the palate, tonsillar pillars, epiglottis, and proximal esophagus
Mechanism of Taste Stimulation:
Interaction of taste substances with receptors on microvilli
Signal transduction pathways for Umami, Sweet, Bitter, Sour, and Salty tastes
Taste Sensitivity and Adaptation:
Decrease in sensitivity with age
Rapid adaptation of taste sensation
Role of Saliva in Taste:
Dissolution of tastants to reach receptors
Washing away the stimulus
Taste Preferences and Aversions:
Mechanisms behind taste preference and aversion
Influence of receptors and neural pathways
Impact of Sensory Nerve Damage:
Degeneration of taste buds if the sensory nerve fiber is cut
Abnormalities of Taste Detection:
Conditions: Ageusia, Hypogeusia, Dysgeusia (parageusia)
Causes: Nerve damage, neurological disorders, infections, poor oral hygiene, adverse drug effects, deficiencies, aging, tobacco use, altered neurotransmitter levels
Neurotransmitters and Taste Threshold:
Effects of serotonin (5-HT) and norepinephrine (NE) on taste sensitivity
Supertasters:
25% of the population with heightened sensitivity to taste, especially bitterness
Increased number of fungiform papillae
Basavarajeeyam is an important text for ayurvedic physician belonging to andhra pradehs. It is a popular compendium in various parts of our country as well as in andhra pradesh. The content of the text was presented in sanskrit and telugu language (Bilingual). One of the most famous book in ayurvedic pharmaceutics and therapeutics. This book contains 25 chapters called as prakaranas. Many rasaoushadis were explained, pioneer of dhatu druti, nadi pareeksha, mutra pareeksha etc. Belongs to the period of 15-16 century. New diseases like upadamsha, phiranga rogas are explained.
Ozempic: Preoperative Management of Patients on GLP-1 Receptor Agonists Saeid Safari
Preoperative Management of Patients on GLP-1 Receptor Agonists like Ozempic and Semiglutide
ASA GUIDELINE
NYSORA Guideline
2 Case Reports of Gastric Ultrasound
- Video recording of this lecture in English language: https://youtu.be/lK81BzxMqdo
- Video recording of this lecture in Arabic language: https://youtu.be/Ve4P0COk9OI
- Link to download the book free: https://nephrotube.blogspot.com/p/nephrotube-nephrology-books.html
- Link to NephroTube website: www.NephroTube.com
- Link to NephroTube social media accounts: https://nephrotube.blogspot.com/p/join-nephrotube-on-social-media.html
Lung Cancer: Artificial Intelligence, Synergetics, Complex System Analysis, S...Oleg Kshivets
RESULTS: Overall life span (LS) was 2252.1±1742.5 days and cumulative 5-year survival (5YS) reached 73.2%, 10 years – 64.8%, 20 years – 42.5%. 513 LCP lived more than 5 years (LS=3124.6±1525.6 days), 148 LCP – more than 10 years (LS=5054.4±1504.1 days).199 LCP died because of LC (LS=562.7±374.5 days). 5YS of LCP after bi/lobectomies was significantly superior in comparison with LCP after pneumonectomies (78.1% vs.63.7%, P=0.00001 by log-rank test). AT significantly improved 5YS (66.3% vs. 34.8%) (P=0.00000 by log-rank test) only for LCP with N1-2. Cox modeling displayed that 5YS of LCP significantly depended on: phase transition (PT) early-invasive LC in terms of synergetics, PT N0—N12, cell ratio factors (ratio between cancer cells- CC and blood cells subpopulations), G1-3, histology, glucose, AT, blood cell circuit, prothrombin index, heparin tolerance, recalcification time (P=0.000-0.038). Neural networks, genetic algorithm selection and bootstrap simulation revealed relationships between 5YS and PT early-invasive LC (rank=1), PT N0—N12 (rank=2), thrombocytes/CC (3), erythrocytes/CC (4), eosinophils/CC (5), healthy cells/CC (6), lymphocytes/CC (7), segmented neutrophils/CC (8), stick neutrophils/CC (9), monocytes/CC (10); leucocytes/CC (11). Correct prediction of 5YS was 100% by neural networks computing (area under ROC curve=1.0; error=0.0).
CONCLUSIONS: 5YS of LCP after radical procedures significantly depended on: 1) PT early-invasive cancer; 2) PT N0--N12; 3) cell ratio factors; 4) blood cell circuit; 5) biochemical factors; 6) hemostasis system; 7) AT; 8) LC characteristics; 9) LC cell dynamics; 10) surgery type: lobectomy/pneumonectomy; 11) anthropometric data. Optimal diagnosis and treatment strategies for LC are: 1) screening and early detection of LC; 2) availability of experienced thoracic surgeons because of complexity of radical procedures; 3) aggressive en block surgery and adequate lymph node dissection for completeness; 4) precise prediction; 5) adjuvant chemoimmunoradiotherapy for LCP with unfavorable prognosis.
2. Lung is porous, highly elastic and
spongy
It crepitates on touch and floats on
water
Color :
-In new born it is rosy pink
-Becomes darker slat grey due to
deposition of carbonacious
particles
Lungs
3. Lungs
Conical in shape, apex, base, costal surface,
medial surface, hilus. Note various impressions
Right lung
Three lobes; superior, middle and inferior
Oblique and horizontal fissure
Left Lung
Two lobes; superior and inferior also Lingula and
Cardiac notch, oblique fissure
4. Lungs Located within the thoracic cavity,
surrounded by the double-layered pleural
membrane –
parietal pleura – lines cavity wall
visceral pleura – covers the lungs
5. Lungs- Anatomical Features
Apex – extends 1” above clavicle
Base – rests on diaphragm
Right
lung Left
lung
Superior
lobe
Middle lobe
Inferior
lobe
Horizontal
fissure
Oblique
fissure
Superior lobe
Inferior lobe
Oblique fissure
Cardiac notch
Hilum – at medial surface;
where primary bronchus,
pulmonary artery & veins
enter/exit lung
9. Each lung has a primary
bronchus entering at the
Hilus.
Each lobe of a lung has a
secondary (a.k.a. lobar)
bronchus
Lobes are functionally
divided into bronchopulmonary
segments & each segment has
a tertiary (segmental)
bronchus
Segments are functionally
divided into many lobules &
each lobule receives a terminal
bronchiole
Airways within Lungs
12. Terminal Bronchioles
16th to 19th generation
Average diameter is 0.5 mm
Cilia and mucous glands begin to
disappear totally
End of the conducting airway
Canals of Lambert-interconnect this
generation,provide collateral ventilation
15. Differences between Bronchi and
Bronchioles
Bronchioles
No glands
No cartilage
No goblet cells
Thick smooth muscle layer
Presence of Clara cells
Many elastic fibres
16. Respiratory Zone
Defined by the presence of alveoli; begins as
terminal bronchioles feed into Respiratory
bronchioles
Respiratory bronchioles lead to alveolar ducts,
then to terminal clusters of alveolar sacs composed
of alveoli
Approximately 300 million alveoli:
Account for most of the lungs’ volume
Provide tremendous surface area for gas exchange
20. Alveoli
200-300 million in a normal lung
Between 75 µ to 300 µ in diameter- Total area-
75 square meters
Most gas exchange takes place at alveolar-
capillary membrane
85-95% of alveoli covered by small pulmonary
capillaries
The cross-sectional area or surface area is
approximately 70m2
21. Alveoli are expanded
chambers of epithelial tissue
that are the exchange
surfaces of the lungs
Multiple alveoli usually share
a common alveolar duct,
creating “alveolar sacs”
22. Acinus or Lobule
Each acinus (unit) is approximately 3.5 mm
in diameter
Each contains about 2000 aveloli
Approximately 130,000 primary lobules in
the lung
25. Alveolar epithelium
Two principle cell types:
Type I cell, squamous pneumocyte
Type II cell, granular pneumocyte
26. Type I Cell (Pneumocytes)
95% of the alveolar surface is made up
of squamous pneumocyte cells
Between 0.1 µ and 0.5µ thick
Major site of gas exchange
Preventing leakage of blood from
capillaries to the alveolar lumen
Form Blood Air barrier
28. Type II Cell
5% of the surface of alveoli composed
of granular pneumocyte cells
Cuboidal in shape with microvilli
Primary source of pulmonary surfactant
Involved with reabsorption of fluids in
the dry, alveolar spaces
29.
30. Type II pneumocytes
Also known as Septal cells
Rounded or cuboidal secretory cells with microvilli
Secretory granules are made of several layers- Multilamellar
bodies.
Is constantly renewed.
Pulmonary Surfactant – is the fluid secreted that spreads
over the alveolar surface.
33. Synthesized by type II alveolar cells
Increase pulmonary compliance.
Reduces surface tension (prevents alveolar collapse during
expiration)
Decreases the force that is needed to inflate alveoli during
inspiration.
Prevent the lung from collapsing at the end of expiration.
Prevents bacterial invasion
Cleans alveoli surface
34. Composition
Lipids : Over 90% of the surfactant
Phosphatidylcholine: ~85% of the lipid in surfactant with
saturated acyl chains.
Phosphatidylglycerol (PG): 11% of the lipids in surfactant
with unsaturated fatty acid chains that fluidize the lipid
monolayer at the interface.
Neutral lipids and cholesterol are also present.
Proteins
10% of surfactant.
35.
36. Surface active agent in water = reduces surface tension
of water on the alveolar walls
Pure water (surface
pressure)
72 dynes/cm
Normal fluid lining alveoli
without surfactant
(surface pressure)
50 dynes/cm
Normal fluid lining alveoli
with surfactant
5-30
dynes/cm
37.
38. Lack of surfactant causes
respiratory distress syndromes
The effect of surfactant on compliance and
elasticity Increase compliance and decrease
elasticity
Premature infants: ordinarily a rise in levels of the
adrenal cortical hormone cortisol induces production
of surfactant before birth.
In some adults with lung trauma from smoke
inhalation or toxic gas, surfactant production is
impaired
39. Canals of Lambert/Pores of Kohn
Provide for collateral ventilation of
difference acinii or primary lobules
Additional ventilation of blocked units
May explain why diseases spread so quickly
at the lung tissue (paremchymal) level
40. Alveolar macrophages
So-called Type III cell
Remove bacteria and foreign particles
May originate as
Stem cells precursors in bone marro
Migrate as monocytes through the blood
and into the lungs
41. Intersitium/interstial space
Surround, supports, and shapes the
alveoli and capillaries
Composed of a gel like substance and
collagen fibers
Contains tight space and loose space
areas
42. Interstitium
Water content in loose space can increase
by 30% before there is a significant change
in pulmonary capillary pressure
Lymphatic drainage easily exceeded
Collagen limits alveolar distensibility
43. Respiratory Membrane
Respiratory membrane
Alveolar wall – type I and type II alveolar cells
Epithelial basement membrane
Capillary basement membrane
Capillary endothelium
Very thin – only 0.5 µm thick to allow rapid diffusion of
gases
Permit gas exchange by simple diffusion
47. Blood Air Barrier
Consist of a thin layer of surfactant
Basement membrane of Pneumocytes I
Basement membrane of capillary endothelial cell
It exists to prevent air bubbles form forming in the blood,
and from blood entering alveoli
48.
49. Nutrition of the lung
The lung gets nutrition from two sources:
1. Conducting part up to the beginning of respiratory
bronchiole is supplied by Bronchial artery
2. Respiratory part is supplied by pulmonary artery via
Pulmonary capillary plexus
• Primary purpose is to deliver blood to lungs for gas
exchange
• Right lung has one bronchial artery and left lung has two
Bronchial artery
50. Bronchial arteries
Also nourish
Mediastinal lymph nodes
Pulmonary nerves
Some muscular pulmonary arteries and
veins
Portions of the esophagus
Visceral pleura
51. Bronchial venous system
1/3 blood returns to right heart
Azygous
Hemiazygous
Intercostal veins
This blood comes form the first two or
three generations of bronchi
52. Bronchial venous return
2/3 of blood flowing to terminal bronchioles drains
into pulmonary circulation via “bronchopulmonary
anastomoses”
Then flows to left atrium via pulmonary veins
Contributes to “venous admixture” or “anatomic
shunt” (ca. 5% of C.O.)
53.
54. Pulmonary Capillaries
Walls are les than 0.1µ thick
Total external thickness is about 10µ
Selective permeability to water,
electrolytes, sugars
Produce and destroy biologically active
substances
55. Lymphatic System
Lymphatic vessels remove
fluids and protein
molecules that leak out of
the pulmonary capillaries
Transfer fluids back into
the circulatory system
56. Lymphatics
Lymphatic vessels arise within loose spaces of
connective tissue, not in the walls of the alveoli.
Vessels then follow bronchial airways,
pulmonary airways, pulmonary arteries and
veins to the hilum
Vessels end in pulmonary and
bronchopulmonary lymph nodes within and
outside of lung parenchyma
57. 57
Pleurae
Serous membrane that covers the lung
parenchyma, mediastinum, diaphragm
and the rib cage
Parietal pleura
Covers the thoracic wall and superior face
of the diaphragm
Continues around heart and between lungs
58. Pleurae
Visceral, or pulmonary, pleura
Covers the external lung surface
Divides the thoracic cavity into three chambers
The central mediastinum
Two lateral compartments, each containing a lung
58
60. Histology
• Grossly: Normal pleura is a smooth, glistening,
semitransparent membrane.
• Light microscopy, pleural consist of five layers :
Mesothalial layer
Connective tissue layer
Superficial elastic layer
Loose subpleural connective tissue layer (rich in
vessels, nerves and lymphatics)
Deep fibroelastic layer (in continuity with the
parenchymal structures of lung, diaphragm or the
thorax)
61. Pleural Fluid
Fluid present between the parietal and visceral pleura, in
space called Pleural fluid.
Fluid act as lubricant and allows the visceral pleura
covering the lung to slide along the parietal pleura lining
the thoracic cavity during respiratory movements.
Volume :
Mean amount of fluid in right pleural space in normal
individual is 8.4 +/- 4.3 ml.
Normally the volume of fluid in right and left pleural
space is equal.
63. Physiochemical factors :
• Protein – Pleural fluid is similar to that of serum except
that low molecular weight protein such as albumin present
in relatively greater quantities in plural fluid.
• Ions :
Bicarbonates : increase by 20-25% to that in plasma.
Sodium : reduce by 3-5% to that in plasma
Chloride : reduce by 6-9% to that in plasma
Potassium : nearly identical to that in plasma
• Glucose : similar to that in plasma- Less than 60 mg/dl .
• Pco2 : same as the plasma Pco2
• pH : due to elevated pleural fluid bicarbonate the pleural
fluid is alkaline with respect to plasma pH.
64.
65.
66. Question
Outline the principal anatomical features of
the diaphragm that are important to its
function.