Smooth muscle cells are found within organs and blood vessels. There are two main types - multi-unit smooth muscle composed of separate fibers, and unitary (visceral) smooth muscle with fibers joined by gap junctions. Smooth muscle contraction is activated by calcium ions and sustained through a latch mechanism using little ATP. Contraction can be stimulated by nerves releasing acetylcholine or norepinephrine, hormones, stretch of the muscle, or local chemical factors and pacemaker potentials in some muscles. Prolonged contraction is enabled through action potentials with plateaus or slow wave potentials.
Molecular basis of Skeletal Muscle ContractionArulSood2
The ppt aims to explain the molecular basis of skeletal muscle contraction and certain applied aspects of the same. Sources include Guyton and Hall's Textbook of Physiology (South-Asia edition, Vol. 2) and C.L. Ghai's Textbook for Practical Physiology.
Molecular basis of Skeletal Muscle ContractionArulSood2
The ppt aims to explain the molecular basis of skeletal muscle contraction and certain applied aspects of the same. Sources include Guyton and Hall's Textbook of Physiology (South-Asia edition, Vol. 2) and C.L. Ghai's Textbook for Practical Physiology.
Skeletal muscle is one of the three significant muscle tissues in the human body. Each skeletal muscle consists of thousands of muscle fibers wrapped together by connective tissue sheaths. The individual bundles of muscle fibers in a skeletal muscle are known as fasciculi.
Describes the overview of the skeletal muscles, its description, functons, and properties. It also inccludes the gross organization of the skeletal system.
The muscle are biological motors which convert chemical energy into force and mechanical work.
This biological machinery is composed of proteins – which is actomyosin and the fuel is ATP.
With the use of muscles we are able to act on our environment.
Muscle is one of the four primary tissue types of the body, and the body contains three types of muscle tissue: skeletal muscle, cardiac muscle, and smooth muscle.
Cardiac muscle (The Guyton and Hall Physiology)Maryam Fida
In the heart there is Atrial muscle and Ventricular muscle which are separated from each other by the fibrous AV Rings containing Valves.
ATRIAL MUSCLE: thin walled. There are two sheets, superficial and deep sheet. Superficial sheet is common over both atria. Deep sheet is separate for each atrium. Muscle fibers in the deep sheet are at right angle to the muscle fibers in the superficial sheet.
FUNCTIONS OF THE ATRIUM:
1. Receive venous blood from large veins. So atria act as reservoir.
2. Conduct the blood into the ventricles.
3. Atrial contraction is responsible for last 25 % of ventricular filling.
4. In the right atrium there is SA Node(Pace maker) and AV node.
5. In the wall of the atria, there are low pressure stretch receptors and these are involved in various reflexes like brain bridge reflex and left atrial reflex.
6. Atria also produce a hormone i.e. Atrial Natriuretic Hormone. Whenever NaCl increases in ECF, it causes release of ANH which causes natriuresis.
VENTRICULAR MUSCLE:
Much thicker than atrial muscle. Thickness of right ventricle wall is 3-4 mm and thickness of left ventricle is 8 – 12 mm.
1.Involuntary
2.Has cross striations
3.Each cardiac muscle fiber consists of a number of cardiac cells, united at ends in series. Where as in skeletal muscle each muscle fiber is individual cell.
4.Cardiac muscle cells are branching and interdigitate.
5.Single central nucleus in each cell.
6. Atrial muscle and ventricular muscle act as separate functional syncytium and impulses from atria are conducted to ventricles through the AV Node and AV Bundle.
7. Sarcoplasmic system is present. In skeletal muscle triad is at the junction of A and I bands. In cardiac muscle T Tubules are much large and thus in cardiac muscle if we take a section it may form a diad or a triad. And these diads and triads are present at the level of Z Disks.
8.Between adjacent cardiac cells there are side to side and end to end connections and these are the intercellular junctions. These junctions are Gap Junctions. Or intercalated discs
9.When one part of myocardium is excited the whole muscle is excited.
10.Whole myocardium obeys all or none law as a whole.
11.No spike potential but action potential with plateau.
12.Has got long refractory period.
Absolute refractory period in ventricular muscle is 250 – 300 milli sec.
In atrial muscle Absolute refractory period is 150 milli sec
Because of long refractory period cardiac muscle cannot be tetanized.
Skeletal muscle is one of the three significant muscle tissues in the human body. Each skeletal muscle consists of thousands of muscle fibers wrapped together by connective tissue sheaths. The individual bundles of muscle fibers in a skeletal muscle are known as fasciculi.
Describes the overview of the skeletal muscles, its description, functons, and properties. It also inccludes the gross organization of the skeletal system.
The muscle are biological motors which convert chemical energy into force and mechanical work.
This biological machinery is composed of proteins – which is actomyosin and the fuel is ATP.
With the use of muscles we are able to act on our environment.
Muscle is one of the four primary tissue types of the body, and the body contains three types of muscle tissue: skeletal muscle, cardiac muscle, and smooth muscle.
Cardiac muscle (The Guyton and Hall Physiology)Maryam Fida
In the heart there is Atrial muscle and Ventricular muscle which are separated from each other by the fibrous AV Rings containing Valves.
ATRIAL MUSCLE: thin walled. There are two sheets, superficial and deep sheet. Superficial sheet is common over both atria. Deep sheet is separate for each atrium. Muscle fibers in the deep sheet are at right angle to the muscle fibers in the superficial sheet.
FUNCTIONS OF THE ATRIUM:
1. Receive venous blood from large veins. So atria act as reservoir.
2. Conduct the blood into the ventricles.
3. Atrial contraction is responsible for last 25 % of ventricular filling.
4. In the right atrium there is SA Node(Pace maker) and AV node.
5. In the wall of the atria, there are low pressure stretch receptors and these are involved in various reflexes like brain bridge reflex and left atrial reflex.
6. Atria also produce a hormone i.e. Atrial Natriuretic Hormone. Whenever NaCl increases in ECF, it causes release of ANH which causes natriuresis.
VENTRICULAR MUSCLE:
Much thicker than atrial muscle. Thickness of right ventricle wall is 3-4 mm and thickness of left ventricle is 8 – 12 mm.
1.Involuntary
2.Has cross striations
3.Each cardiac muscle fiber consists of a number of cardiac cells, united at ends in series. Where as in skeletal muscle each muscle fiber is individual cell.
4.Cardiac muscle cells are branching and interdigitate.
5.Single central nucleus in each cell.
6. Atrial muscle and ventricular muscle act as separate functional syncytium and impulses from atria are conducted to ventricles through the AV Node and AV Bundle.
7. Sarcoplasmic system is present. In skeletal muscle triad is at the junction of A and I bands. In cardiac muscle T Tubules are much large and thus in cardiac muscle if we take a section it may form a diad or a triad. And these diads and triads are present at the level of Z Disks.
8.Between adjacent cardiac cells there are side to side and end to end connections and these are the intercellular junctions. These junctions are Gap Junctions. Or intercalated discs
9.When one part of myocardium is excited the whole muscle is excited.
10.Whole myocardium obeys all or none law as a whole.
11.No spike potential but action potential with plateau.
12.Has got long refractory period.
Absolute refractory period in ventricular muscle is 250 – 300 milli sec.
In atrial muscle Absolute refractory period is 150 milli sec
Because of long refractory period cardiac muscle cannot be tetanized.
skeletal, cardiac & smooth Muscles by Thiru Murugan.pptxthiru murugan
Unit III – The Muscular System - Anatomy
Types and structure of muscles
Muscle groups
Alterations in disease
Applications and implications in nursing
Muscle:
Muscle is a soft tissue and it is one of the 4 basic tissues, along with nervous tissue, epithelium, and connective tissue.
Muscles helps in movement, support and protection of internal organs.
Muscles can perform variety of functions
Muscles tissue is made up of cells called “MYOCYTES” or muscle fibers.
There are more than 600 muscles in the human body. A kind of elastic tissue makes up each muscle, which consists of thousands, or tens of thousands, of small muscle fibers.
Types of Muscles: There are 3 main types of muscles
Skeletal muscle
Cardiac muscle
Smooth muscle
Skeletal muscle:
These are having close relationship to the bone or skeleton, so called Skeletal muscles
It present in limbs and related body parts & It form about 40% of body weight.
Under microscope the skeletal muscles fibers shows prominent striations, so called “Striated Muscles” & It is also known as “Voluntary Muscles” (movements are under our control)
Structure of Skeletal muscle:
Muscle fibers shows transverse striations under light microscope so it is called “striated muscles”
The nucleus is located peripherally.
Each skeletal muscle is an organ that consists of numerous cells called muscle fibers.
Each muscle fibers surrounded by “ Endomysium”
Inside each skeletal muscle, muscle fibers are organized into bundles, called fascicles, each fascicle surrounded by perimysium.
The whole muscle is covered by “epimysium”
Each skeletal muscle has three layers: endomysium, perimysium and epimysium
Muscle fibers:
Muscle is composed of many long cylindrical-shaped elongated fibres called muscle fibers
Length varies according to the size and shape of the muscles.
The actual arrangement of the fibres depending on the function of the muscle.
Each muscle fibers covered by a membrane is called the sarcolemma.
The cytoplasm of a muscle fiber is called Sarcoplasm
In sarcoplasm there are many mitochondria and bundles of fine longitudinal thread like part is called “myofibrils”
Microscopic structure of myofibrils:
A myofibril (also known as a muscle fibril or sarcostyle) is a basic rod-like part of a muscle cell.
Muscles are composed of tubular cells called myocytes, known as muscle fibres in striated muscle, and these cells in turn contain many chains of myofibrils.
They are created during embryonic development in a process known as myogenesis.
Under light microscope each myofibril consist of 2 bands:
Light band or “I” Band and Dark band or “A” Band
The alternating pattern of these bands results in the striated appearance of skeletal muscle.
Light band or “I” Band:
The I-bands (isotropic in polarized light) appear light in color.
I band divided into 2 portions by a narrow dark line called “Z” line or “Z” Disc.
This “Z” line is formed by protein which does not permit the light.
The part in between 2 “Z” lines called “sarc
Learn about how our muscle functioning everyday. And check out the muscle roles!! Simple notes, Simple slides for the beginner person who's attracted to science.
2. Unit - 7-Muscles Anatomy, Thiru Murugan, Msc Professorthiru murugan
The Muscular System
By Thiru murugan. M
The Muscular system:
Types and structure of muscles
Muscle groups: muscles of the head, neck, thorax, abdomen, pelvis, upper limb and lower limbs
Principal muscles: deltoid, biceps, triceps, respiratory, abdominal, pelvic floor, pelvic floor muscles, gluteal muscles and vastus lateralis
Major muscles involved in nursing procedures
Muscle:
Muscle is a soft tissue and it is one of the 4 basic tissues, along with nervous tissue, epithelium, and connective tissue.
Muscles helps in movement, support and protection of internal organs.
Muscles can perform variety of functions
Muscles tissue is made up of cells called “MYOCYTES” or muscle fibers.
There are more than 600 muscles in the human body. A kind of elastic tissue makes up each muscle, which consists of thousands, or tens of thousands, of small muscle fibers.
Types of Muscles: There are 3 main types of muscles
Skeletal muscle
Cardiac muscle
Smooth muscle
Skeletal muscle:
These are having close relationship to the bone or skeleton, so called Skeletal muscles
It present in limbs and related body parts & It form about 40% of body weight.
Under microscope the skeletal muscles fibers shows prominent striations, so called “Striated Muscles” & It is also known as “Voluntary Muscles” (movements are under our control)
Structure of Skeletal muscle:
Muscle fibers shows transverse striations under light microscope so it is called “striated muscles”
The nucleus is located peripherally.
Each skeletal muscle is an organ that consists of numerous cells called muscle fibers.
Each muscle fibers surrounded by “ Endomysium”
Inside each skeletal muscle, muscle fibers are organized into bundles, called fascicles, each fascicle surrounded by perimysium.
The whole muscle is covered by “epimysium”
Each skeletal muscle has three layers: endomysium, perimysium and epimysium
Muscle fibers:
Muscle is composed of many long cylindrical-shaped elongated fibres called muscle fibers
Length varies according to the size and shape of the muscles.
The actual arrangement of the fibres depending on the function of the muscle.
Each muscle fibers covered by a membrane is called the sarcolemma.
The cytoplasm of a muscle fiber is called Sarcoplasm
In sarcoplasm there are many mitochondria and bundles of fine longitudinal thread like part is called “myofibrils”
Microscopic structure of myofibrils:
A myofibril (also known as a muscle fibril or sarcostyle) is a basic rod-like part of a muscle cell.
Muscles are composed of tubular cells called myocytes, known as muscle fibres in striated muscle, and these cells in turn contain many chains of myofibrils.
They are created during embryonic development in a process known as myogenesis.
Under light microscope each myofibril consist of 2 bands:
Light band or “I” Band & Dark band or “A” Band
The alternating pattern of these bands results in the striated appearance of skeletal muscle.
Light band or “I” Band:
The I-bands (isotropic in polarize
Common medication used for anesthesia, there action; dosage; adverse effect; duration of action.
They Include {inhalation + Induction + Muscle relaxant + Anticholinergic + Analgesic + Resuscitation}
in this presentation lecture we gone take a hypo and hyper thyrodism that affect the human cell because both situation may increase or decrease the basal metabolic rate.
When the pituitary Gland it' s function is increased whether the cause are?
Both anterior and Posterior gland secretions are increased the most causes are ADENOMAS
in this presentation you will be learn the different drug form that all medical health workers prescribing the medication.
the medical student should have a good knowledge and keep in mind these drug forms based on medical administration the drugs are classified into invasive (injection and transdermal implantation) and non invasive (oral, inhalers, suppository)
Medical equipment and tools are crucial to saving a person's life or performing any procedure.
i presented here the most and commonly equipment used by medical student to improve their skills
This note paper is short notes of general physiology for medical students who which to understand the concept of the physiology, physiology is the mother of medicine.
A summary of skeletal muscle contraction and relaxationAyub Abdi
it consist for 4 pages and cover all the steps that occur during muscle contraction and relaxation, I does not take a time just 5 minute is enough to read. I hope it's interesting.
Title: Sense of Smell
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 primary categories of smells and the concept of odor blindness.
Explain the structure and location of the olfactory membrane and mucosa, including the types and roles of cells involved in olfaction.
Describe the pathway and mechanisms of olfactory signal transmission from the olfactory receptors to the brain.
Illustrate the biochemical cascade triggered by odorant binding to olfactory receptors, including the role of G-proteins and second messengers in generating an action potential.
Identify different types of olfactory disorders such as anosmia, hyposmia, hyperosmia, and dysosmia, including their potential causes.
Key Topics:
Olfactory Genes:
3% of the human genome accounts for olfactory genes.
400 genes for odorant receptors.
Olfactory Membrane:
Located in the superior part of the nasal cavity.
Medially: Folds downward along the superior septum.
Laterally: Folds over the superior turbinate and upper surface of the middle turbinate.
Total surface area: 5-10 square centimeters.
Olfactory Mucosa:
Olfactory Cells: Bipolar nerve cells derived from the CNS (100 million), with 4-25 olfactory cilia per cell.
Sustentacular Cells: Produce mucus and maintain ionic and molecular environment.
Basal Cells: Replace worn-out olfactory cells with an average lifespan of 1-2 months.
Bowman’s Gland: Secretes mucus.
Stimulation of Olfactory Cells:
Odorant dissolves in mucus and attaches to receptors on olfactory cilia.
Involves a cascade effect through G-proteins and second messengers, leading to depolarization and action potential generation in the olfactory nerve.
Quality of a Good Odorant:
Small (3-20 Carbon atoms), volatile, water-soluble, and lipid-soluble.
Facilitated by odorant-binding proteins in mucus.
Membrane Potential and Action Potential:
Resting membrane potential: -55mV.
Action potential frequency in the olfactory nerve increases with odorant strength.
Adaptation Towards the Sense of Smell:
Rapid adaptation within the first second, with further slow adaptation.
Psychological adaptation greater than receptor adaptation, involving feedback inhibition from the central nervous system.
Primary Sensations of Smell:
Camphoraceous, Musky, Floral, Pepperminty, Ethereal, Pungent, Putrid.
Odor Detection Threshold:
Examples: Hydrogen sulfide (0.0005 ppm), Methyl-mercaptan (0.002 ppm).
Some toxic substances are odorless at lethal concentrations.
Characteristics of Smell:
Odor blindness for single substances due to lack of appropriate receptor protein.
Behavioral and emotional influences of smell.
Transmission of Olfactory Signals:
From olfactory cells to glomeruli in the olfactory bulb, involving lateral inhibition.
Primitive, less old, and new olfactory systems with different path
Pulmonary Thromboembolism - etilogy, types, medical- Surgical and nursing man...VarunMahajani
Disruption of blood supply to lung alveoli due to blockage of one or more pulmonary blood vessels is called as Pulmonary thromboembolism. In this presentation we will discuss its causes, types and its management in depth.
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.
New Directions in Targeted Therapeutic Approaches for Older Adults With Mantl...i3 Health
i3 Health is pleased to make the speaker slides from this activity available for use as a non-accredited self-study or teaching resource.
This slide deck presented by Dr. Kami Maddocks, Professor-Clinical in the Division of Hematology and
Associate Division Director for Ambulatory Operations
The Ohio State University Comprehensive Cancer Center, will provide insight into new directions in targeted therapeutic approaches for older adults with mantle cell lymphoma.
STATEMENT OF NEED
Mantle cell lymphoma (MCL) is a rare, aggressive B-cell non-Hodgkin lymphoma (NHL) accounting for 5% to 7% of all lymphomas. Its prognosis ranges from indolent disease that does not require treatment for years to very aggressive disease, which is associated with poor survival (Silkenstedt et al, 2021). Typically, MCL is diagnosed at advanced stage and in older patients who cannot tolerate intensive therapy (NCCN, 2022). Although recent advances have slightly increased remission rates, recurrence and relapse remain very common, leading to a median overall survival between 3 and 6 years (LLS, 2021). Though there are several effective options, progress is still needed towards establishing an accepted frontline approach for MCL (Castellino et al, 2022). Treatment selection and management of MCL are complicated by the heterogeneity of prognosis, advanced age and comorbidities of patients, and lack of an established standard approach for treatment, making it vital that clinicians be familiar with the latest research and advances in this area. In this activity chaired by Michael Wang, MD, Professor in the Department of Lymphoma & Myeloma at MD Anderson Cancer Center, expert faculty will discuss prognostic factors informing treatment, the promising results of recent trials in new therapeutic approaches, and the implications of treatment resistance in therapeutic selection for MCL.
Target Audience
Hematology/oncology fellows, attending faculty, and other health care professionals involved in the treatment of patients with mantle cell lymphoma (MCL).
Learning Objectives
1.) Identify clinical and biological prognostic factors that can guide treatment decision making for older adults with MCL
2.) Evaluate emerging data on targeted therapeutic approaches for treatment-naive and relapsed/refractory MCL and their applicability to older adults
3.) Assess mechanisms of resistance to targeted therapies for MCL and their implications for treatment selection
ARTIFICIAL INTELLIGENCE IN HEALTHCARE.pdfAnujkumaranit
Artificial intelligence (AI) refers to the simulation of human intelligence processes by machines, especially computer systems. It encompasses tasks such as learning, reasoning, problem-solving, perception, and language understanding. AI technologies are revolutionizing various fields, from healthcare to finance, by enabling machines to perform tasks that typically require human intelligence.
Ethanol (CH3CH2OH), or beverage alcohol, is a two-carbon alcohol
that is rapidly distributed in the body and brain. Ethanol alters many
neurochemical systems and has rewarding and addictive properties. It
is the oldest recreational drug and likely contributes to more morbidity,
mortality, and public health costs than all illicit drugs combined. The
5th edition of the Diagnostic and Statistical Manual of Mental Disorders
(DSM-5) integrates alcohol abuse and alcohol dependence into a single
disorder called alcohol use disorder (AUD), with mild, moderate,
and severe subclassifications (American Psychiatric Association, 2013).
In the DSM-5, all types of substance abuse and dependence have been
combined into a single substance use disorder (SUD) on a continuum
from mild to severe. A diagnosis of AUD requires that at least two of
the 11 DSM-5 behaviors be present within a 12-month period (mild
AUD: 2–3 criteria; moderate AUD: 4–5 criteria; severe AUD: 6–11 criteria).
The four main behavioral effects of AUD are impaired control over
drinking, negative social consequences, risky use, and altered physiological
effects (tolerance, withdrawal). This chapter presents an overview
of the prevalence and harmful consequences of AUD in the U.S.,
the systemic nature of the disease, neurocircuitry and stages of AUD,
comorbidities, fetal alcohol spectrum disorders, genetic risk factors, and
pharmacotherapies for AUD.
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
2. Smooth Muscle Cell:
• 1 to 5 micrometers in
diameter and only 20 to
500 micrometers in
length.
• The same attractive
forces between myosin
and actin filaments.
• The internal physical
arrangement of smooth
muscle fibers is different.
3. TYPES OF SMOOTH MUSCLE:
• The smooth muscle of each organ is distinctive from
that of most other organs in several ways:
(1) Physical dimensions.
(2) Organization into bundles or sheets.
(3) Response to different types of stimuli.
(4) Characteristics of innervation.
(5) Function.
• Smooth muscle can generally be divided into two
major types:
A. multi-unit smooth muscle.
B. unitary (or single-unit) smooth muscle.
4.
5. A. Multi-Unit Smooth Muscle:
• Composed of discrete, separate smooth muscle fibers.
• Operates independently of the others.
• Is innervated by a single nerve ending.
• Covered by outer surface of fiber covered by a thin layer of
basement membrane–like substance, a mixture of fine
collagen and glycoprotein that helps insulate the separate
fibers from one another.
• Some examples of multi-unit smooth muscle are:
A. Ciliary muscle of the eye.
B. The iris muscle of the eye.
C. The piloerector muscles that cause erection of the hairs.
6. B. Unitary Smooth Muscle:
• Also called syncytial smooth muscle or visceral smooth
muscle.
• A mass of hundreds to thousands of smooth muscle fibers
that contract together as a single unit.
• The fibers usually are arranged in sheets or bundles.
• The cell membranes are joined by many gap junctions.
• It is found in the walls of most viscera of the body,
including:
A. Gastrointestinal tract,
B. Bile ducts,
C. Ureters,
D. Uterus,
E. Many blood vessels.
7. CONTRACTILE MECHANISM
IN SMOOTH MUSCLE:
a) Smooth muscle
contains both actin
and myosin filaments.
b) It does not contain the
troponin complex.
c) the contractile process
is activated by
calcium ions, and
adenosine
triphosphate (ATP) –
ADP.
8. Comparison of Smooth Muscle Contraction
and Skeletal Muscle Contraction:
• Most skeletal muscles contract and relax rapidly, most smooth muscle
contraction is prolonged tonic contraction, sometimes lasting hours or
even days.
1. Slow Cycling of the Myosin Cross-Bridges (Actin - myosin).
2. Low Energy Requirement to Sustain Smooth Muscle Contraction (ATP).
3. Slowness of Onset of Contraction and Relaxation of the Total Smooth
Muscle Tissue.
4. The Maximum Force of Contraction Is Often Greater in Smooth
Muscle Than in Skeletal Muscle.
5. The “Latch” Mechanism Facilitates Prolonged Holding of Contractions
of Smooth Muscle (maintain prolonged tonic contraction in smooth
muscle for hours with little use of energy).
6. Stress-Relaxation of Smooth Muscle (maintain about the same amount
of pressure inside its lumen despite sustained, large changes in
volume.).
9. Activation and subsequent contraction occur in
the following sequence:
1. Calcium concentration in the cytosolic fluid of the smooth muscle
increases as a result of the influx of calcium from the extracellular fluid
through calcium channels and/or release of calcium from the
sarcoplasmic reticulum.
2. The calcium ions bind reversibly with calmodulin.
3. The calmodulin-calcium complex then joins with and activates myosin
light chain kinase, a phosphorylating enzyme.
4. One of the light chains of each myosin head, called the regulatory chain,
becomes phosphorylated in response to this myosin kinase.
When this chain is not phosphorylated, the attachment-detachment cycling
of the myosin head with the actin filament does not occur.
However, when the regulatory chain is phosphorylated, the head has the
capability of binding repetitively with the actin filament and proceeding
through the entire cycling process of intermittent “pulls”
12. A Calcium Pump Is Required to
Cause Smooth Muscle Relaxation.
Myosin Phosphatase Is Important
in Cessation of Contraction.
13. NERVOUS AND HORMONAL CONTROL
OF SMOOTH MUSCLE CONTRACTION
• Smooth muscle can be stimulated to contract by:
1. Nervous signals.
2. Hormonal stimulation.
3. Stretch of the muscle.
4. Several other ways.
• The smooth muscle membrane contains many types:
A. Receptor proteins that can initiate the contractile
process.
B. Still other receptor proteins inhibit smooth muscle
contraction.
14. NEUROMUSCULAR JUNCTIONS
OF SMOOTH MUSCLE:
the vesicles of the autonomic nerve
fiber endings contain acetylcholine
in some fibers and norepinephrine in
others, and occasionally other
substances as well.
Contact junctions
Diffuse junctions
the rapidity of contraction of these
smooth muscle fibers is considerably
faster than that of fibers stimulated
by the diffuse junctions.
Acetylcholine is an excitatory transmitter
substance for smooth muscle fibers in
some organs but an inhibitory transmitter
for smooth muscle in other organs. When
acetylcholine excites a muscle fiber,
norepinephrine ordinarily inhibits it.
Conversely, when acetylcholine inhibits a
fiber, norepinephrine usually excites it.
15. MEMBRANE POTENTIALS AND ACTION
POTENTIALS IN SMOOTH MUSCLE
• In the normal resting state, the intracellular
potential is usually about −50 to −60 millivolts.
• Action Potentials in Unitary Smooth Muscle:
• Same way that they occur in skeletal muscle.
• Not normally occur in most multi-unit types of
smooth muscle.
• The action potentials of visceral smooth muscle
occur in one of two forms:
(1) Spike potentials.
(2) Action potentials with plateaus.
16. Spike Potentials:
• The duration of this type of action potential is 10 to 50
milliseconds.
• In Unitary Smooth muscle
• Action potentials can be elicited in many ways:
1. Elicited by electrical stimulation:
2. Action of hormones.
3. Action of transmitter substances from nerve
fibers.
4. By stretch.
5. Spontaneous generation in the muscle fiber
itself
17. Action Potentials with
Plateaus:
• Similar to that of the typical spike potential.
• The repolarization is delayed for several hundred to
as much as 1000 milliseconds (1 second).
• The importance of the plateau is that it can account
for the prolonged contraction that occurs in some
types of smooth muscle:
A. Ureter.
B. The uterus under some conditions.
C. certain types of vascular smooth muscle.
D. Also seen in cardiac muscle fibers that have a
prolonged period of contraction.
18. Slow Wave Potentials in Unitary Smooth
Muscle Can Lead to Spontaneous
Generation of Action Potentials
• Some smooth muscle is self-excitatory
(Pacemaker)—that is, action potentials arise within
the smooth muscle cells without an extrinsic
stimulus.
• This activity is often associated with a basic slow
wave rhythm of the membrane potential.
• The slow wave itself is not the action potential.
• It is a local property of the smooth muscle fibers that
make up the muscle mass.
• The slow waves are caused by waxing and waning of
the pumping of positive ions (presumably sodium
ions) outward through the muscle fiber membrane.
19. Continueeeeeeeeee.
• The conductances of the ion channels increase and
decrease rhythmically.
• The slow waves is that, when they are strong enough,
they can initiate action potentials.
• The slow waves themselves cannot cause muscle
contraction.
• When the peak of the negative slow wave potential
inside the cell membrane rises in the positive direction
from −60 to about −35 millivolts an action potential
develops and spreads over the muscle mass and
contraction occurs.
• The slow waves are called pacemaker waves.
20. Excitation of Visceral Smooth
Muscle by Muscle Stretch:
• When visceral (unitary) smooth muscle is
stretched sufficiently, spontaneous action
potentials are usually generated.
• They result from a combination of
(1) The normal slow wave potentials
(2) A decrease in overall negativity of the
membrane potential caused by the stretch.
• This response to stretch allows the gut wall, when
excessively stretched, to contract automatically
and rhythmically.
22. • The smooth muscle fibers of multi-unit smooth muscle
normally contract mainly in response to nerve stimuli.
• The transmitter substances cause depolarization of the
smooth muscle membrane, and this depolarization in turn
elicits contraction.
• Action potentials usually do not develop because the fibers
are too small to generate an action potential.
• Yet in small smooth muscle cells, even without an action
potential, the local depolarization (called the junctional
potential) caused by the nerve transmitter substance itself
spreads “electrotonically” over the entire fiber and is all
that is necessary to cause muscle contraction.
23. • Approximately half of all smooth muscle
contraction is likely initiated by stimulatory
factors acting directly on the smooth muscle
contractile machinery and without action
potentials.
• Two types of non-nervous and non - action
potential stimulating factors often involved are:
(1) local tissue chemical factors (humoral)
(2) various hormones.
24. Smooth Muscle Contraction in Response to
Local Tissue Chemical Factors
• Some of the specific control factors are as follows:
1. Lack of oxygen in the local tissues causes smooth muscle
relaxation and, therefore, vasodilation.
2. Excess carbon dioxide causes vasodilation.
3. Increased hydrogen ion concentration causes vasodilation.
4. Adenosine, lactic acid, increased potassium ions,
diminished calcium ion concentration, and increased body
temperature can all cause local vasodilation.
5. Decreased blood pressure, by causing decreased stretch of
the vascular smooth muscle, also causes these small blood
vessels to dilate.
6. Nitric oxide (NO), the endothelium-derived relaxing factor
(EDRF).
25. Effects of Hormones on
Smooth Muscle Contraction:
1. Norepinephrine,
2. Epinephrine,
3. Acetylcholine
4. Angiotensin II,
5. Endothelin,
6. Vasopressin,
7. Oxytocin,
8. Serotonin,
9. Histamine.