Intestines(movements and secretions of small and large intestines ) The Guyto...Maryam Fida
Intestines(movements and secretions of small and large intestines)
Distended Portion of small intestine with chyme stretching concentric contractions at intervals lasting a fraction of a minute These contraction causes “Segmentation” of the small intestine ---forms spaced segments new points every time chopping chyme 2-3 times/min mixing with intestinal secretions maximum frequencyof segmentation contraction depends on frequency of BER (Basic electrical rhythm) i.e. In duodenum and proximal jejunum is 12/min and in terminal ileum is 8-9/min.
Atropine blocks the segmentation
law of gut
The peristaltic reflex +anal direction of movement of the peristalsis is called “LAW OF GUT”
Intestines(movements and secretions of small and large intestines ) The Guyto...Maryam Fida
Intestines(movements and secretions of small and large intestines)
Distended Portion of small intestine with chyme stretching concentric contractions at intervals lasting a fraction of a minute These contraction causes “Segmentation” of the small intestine ---forms spaced segments new points every time chopping chyme 2-3 times/min mixing with intestinal secretions maximum frequencyof segmentation contraction depends on frequency of BER (Basic electrical rhythm) i.e. In duodenum and proximal jejunum is 12/min and in terminal ileum is 8-9/min.
Atropine blocks the segmentation
law of gut
The peristaltic reflex +anal direction of movement of the peristalsis is called “LAW OF GUT”
anatomy of large intestine, its section, ceacum, ascending colon, transverse colon, descending colon, sigmoid colon, functions of large intestine , relations of each components of large intestine, carddinal siggns of large intestine, iliocecal junstion, difference between large and small intestine. abdominal angina, superior mesenteric and inferior mesenteric artery, lymphatic drainage, colonoscophy,
THIS PRESENTATION INCLUDES DETAILED INFORMATION ABOUT ACCESSORY ORGANS OF DIGESTIVE SYSTEM..i,e TEETH, TONGUE, SALIVARY GLANDS, PANCREAS, LIVER AND GALL BLADDER
anatomy of large intestine, its section, ceacum, ascending colon, transverse colon, descending colon, sigmoid colon, functions of large intestine , relations of each components of large intestine, carddinal siggns of large intestine, iliocecal junstion, difference between large and small intestine. abdominal angina, superior mesenteric and inferior mesenteric artery, lymphatic drainage, colonoscophy,
THIS PRESENTATION INCLUDES DETAILED INFORMATION ABOUT ACCESSORY ORGANS OF DIGESTIVE SYSTEM..i,e TEETH, TONGUE, SALIVARY GLANDS, PANCREAS, LIVER AND GALL BLADDER
FUNCTIONAL ANATOMY
INTESTINAL VILLI AND GLANDS
PROPERTIES AND COMPOSITION OF SUCCUS ENTERICUS
FUNCTIONS OF SUCCUS ENTERICUS
FUNCTIONS OF SMALL INTESTINE
REGULATION OF SECRETION OF SUCCUS ENTERICUS
METHODS OF COLLECTION OF SUCCUS ENTERICUS
APPLIED PHYSIOLOGY
Experiment 10 –Enzymes
Enzymes are proteins that act as catalysts for biological reactions. Enzymes, like
all catalysts, speed up reactions without being used up themselves. They do this by
lowering the activation energy of a reaction. All biochemical reactions are catalyzed by
enzymes. Since enzymes are proteins, they can be denatured in a variety of ways, so they
are most active under mild conditions. Most enzymes have optimum activity at a neutral
pH and at body temperature.
Enzymes are also very specific –they only act on one substrate or one class of
related substrate molecules. The reason for this is that the active site of the enzyme is
complementary to the shape and polarity of the substrate. Typically, only one kind of
substrate will “fit” into the active site.
In this experiment, we will work with the enzyme amylase. This enzyme is
responsible for hydrolyzing starch. In the presence of amylase, a sample of starch will be
hydrolyzed to shorter polysaccharides, dextrins, maltose, and glucose. The extent of the
hydrolysis depends on how long it is allowed to react –if the starch is hydrolyzed
completely, the resulting product is glucose.
You will test for the presence or absence of starch in the solutions using iodine
(I2). Iodine forms a blue to black complex with starch, but does not react with glucose. If
iodine is added to a glucose solution, the only color seen is the red or yellow color of the
iodine. Therefore, the faster the blue color of starch is lost, the faster the enzyme amylase
is working. If the amylase is inactivated, it can no longer hydrolyze starch, so the blue
color of the starch-iodine complex will persist.
You will also test for the presence of glucose in the samples using Benedict’s
reagent. When a blue solution of Benedict’s reagent is added to a glucose solution, the
color will change to green (at low glucose concentrations) or reddish-orange (at higher
glucose concentrations). Starch will not react with Benedict’s reagent, so the solution will
remain blue.
Professional air quality monitoring systems provide immediate, on-site data for analysis, compliance, and decision-making.
Monitor common gases, weather parameters, particulates.
Slide 1: Title Slide
Extrachromosomal Inheritance
Slide 2: Introduction to Extrachromosomal Inheritance
Definition: Extrachromosomal inheritance refers to the transmission of genetic material that is not found within the nucleus.
Key Components: Involves genes located in mitochondria, chloroplasts, and plasmids.
Slide 3: Mitochondrial Inheritance
Mitochondria: Organelles responsible for energy production.
Mitochondrial DNA (mtDNA): Circular DNA molecule found in mitochondria.
Inheritance Pattern: Maternally inherited, meaning it is passed from mothers to all their offspring.
Diseases: Examples include Leber’s hereditary optic neuropathy (LHON) and mitochondrial myopathy.
Slide 4: Chloroplast Inheritance
Chloroplasts: Organelles responsible for photosynthesis in plants.
Chloroplast DNA (cpDNA): Circular DNA molecule found in chloroplasts.
Inheritance Pattern: Often maternally inherited in most plants, but can vary in some species.
Examples: Variegation in plants, where leaf color patterns are determined by chloroplast DNA.
Slide 5: Plasmid Inheritance
Plasmids: Small, circular DNA molecules found in bacteria and some eukaryotes.
Features: Can carry antibiotic resistance genes and can be transferred between cells through processes like conjugation.
Significance: Important in biotechnology for gene cloning and genetic engineering.
Slide 6: Mechanisms of Extrachromosomal Inheritance
Non-Mendelian Patterns: Do not follow Mendel’s laws of inheritance.
Cytoplasmic Segregation: During cell division, organelles like mitochondria and chloroplasts are randomly distributed to daughter cells.
Heteroplasmy: Presence of more than one type of organellar genome within a cell, leading to variation in expression.
Slide 7: Examples of Extrachromosomal Inheritance
Four O’clock Plant (Mirabilis jalapa): Shows variegated leaves due to different cpDNA in leaf cells.
Petite Mutants in Yeast: Result from mutations in mitochondrial DNA affecting respiration.
Slide 8: Importance of Extrachromosomal Inheritance
Evolution: Provides insight into the evolution of eukaryotic cells.
Medicine: Understanding mitochondrial inheritance helps in diagnosing and treating mitochondrial diseases.
Agriculture: Chloroplast inheritance can be used in plant breeding and genetic modification.
Slide 9: Recent Research and Advances
Gene Editing: Techniques like CRISPR-Cas9 are being used to edit mitochondrial and chloroplast DNA.
Therapies: Development of mitochondrial replacement therapy (MRT) for preventing mitochondrial diseases.
Slide 10: Conclusion
Summary: Extrachromosomal inheritance involves the transmission of genetic material outside the nucleus and plays a crucial role in genetics, medicine, and biotechnology.
Future Directions: Continued research and technological advancements hold promise for new treatments and applications.
Slide 11: Questions and Discussion
Invite Audience: Open the floor for any questions or further discussion on the topic.
Richard's aventures in two entangled wonderlandsRichard Gill
Since the loophole-free Bell experiments of 2020 and the Nobel prizes in physics of 2022, critics of Bell's work have retreated to the fortress of super-determinism. Now, super-determinism is a derogatory word - it just means "determinism". Palmer, Hance and Hossenfelder argue that quantum mechanics and determinism are not incompatible, using a sophisticated mathematical construction based on a subtle thinning of allowed states and measurements in quantum mechanics, such that what is left appears to make Bell's argument fail, without altering the empirical predictions of quantum mechanics. I think however that it is a smoke screen, and the slogan "lost in math" comes to my mind. I will discuss some other recent disproofs of Bell's theorem using the language of causality based on causal graphs. Causal thinking is also central to law and justice. I will mention surprising connections to my work on serial killer nurse cases, in particular the Dutch case of Lucia de Berk and the current UK case of Lucy Letby.
Multi-source connectivity as the driver of solar wind variability in the heli...Sérgio Sacani
The ambient solar wind that flls the heliosphere originates from multiple
sources in the solar corona and is highly structured. It is often described
as high-speed, relatively homogeneous, plasma streams from coronal
holes and slow-speed, highly variable, streams whose source regions are
under debate. A key goal of ESA/NASA’s Solar Orbiter mission is to identify
solar wind sources and understand what drives the complexity seen in the
heliosphere. By combining magnetic feld modelling and spectroscopic
techniques with high-resolution observations and measurements, we show
that the solar wind variability detected in situ by Solar Orbiter in March
2022 is driven by spatio-temporal changes in the magnetic connectivity to
multiple sources in the solar atmosphere. The magnetic feld footpoints
connected to the spacecraft moved from the boundaries of a coronal hole
to one active region (12961) and then across to another region (12957). This
is refected in the in situ measurements, which show the transition from fast
to highly Alfvénic then to slow solar wind that is disrupted by the arrival of
a coronal mass ejection. Our results describe solar wind variability at 0.5 au
but are applicable to near-Earth observatories.
The increased availability of biomedical data, particularly in the public domain, offers the opportunity to better understand human health and to develop effective therapeutics for a wide range of unmet medical needs. However, data scientists remain stymied by the fact that data remain hard to find and to productively reuse because data and their metadata i) are wholly inaccessible, ii) are in non-standard or incompatible representations, iii) do not conform to community standards, and iv) have unclear or highly restricted terms and conditions that preclude legitimate reuse. These limitations require a rethink on data can be made machine and AI-ready - the key motivation behind the FAIR Guiding Principles. Concurrently, while recent efforts have explored the use of deep learning to fuse disparate data into predictive models for a wide range of biomedical applications, these models often fail even when the correct answer is already known, and fail to explain individual predictions in terms that data scientists can appreciate. These limitations suggest that new methods to produce practical artificial intelligence are still needed.
In this talk, I will discuss our work in (1) building an integrative knowledge infrastructure to prepare FAIR and "AI-ready" data and services along with (2) neurosymbolic AI methods to improve the quality of predictions and to generate plausible explanations. Attention is given to standards, platforms, and methods to wrangle knowledge into simple, but effective semantic and latent representations, and to make these available into standards-compliant and discoverable interfaces that can be used in model building, validation, and explanation. Our work, and those of others in the field, creates a baseline for building trustworthy and easy to deploy AI models in biomedicine.
Bio
Dr. Michel Dumontier is the Distinguished Professor of Data Science at Maastricht University, founder and executive director of the Institute of Data Science, and co-founder of the FAIR (Findable, Accessible, Interoperable and Reusable) data principles. His research explores socio-technological approaches for responsible discovery science, which includes collaborative multi-modal knowledge graphs, privacy-preserving distributed data mining, and AI methods for drug discovery and personalized medicine. His work is supported through the Dutch National Research Agenda, the Netherlands Organisation for Scientific Research, Horizon Europe, the European Open Science Cloud, the US National Institutes of Health, and a Marie-Curie Innovative Training Network. He is the editor-in-chief for the journal Data Science and is internationally recognized for his contributions in bioinformatics, biomedical informatics, and semantic technologies including ontologies and linked data.
3. There are two types movements of small intestine
1. MIXING CONTRACTIONS
(SEGMENTATION
CONTRATIONS)
2. PROPULSIVE CONTRACTIONS
4. Segmentation movements
Distension of small intestine with chyme stretches the intestinal
wall and initiates segmentation movements
There are localized concentric contractions (about 1-2 cm in
length) spaced at intervals along the intestine. They divide the
intestine into spaced segments.
As one set of segmentation contractions relaxes, a new set often
begins, but the contractions this time occur mainly at new points
between the previous contractions.
5. the segmentation contractions “chop” the chyme two to three times per
minute, in this way promoting progressive mixing of the food with secretions of
the small intestine.
The maximum frequency of the segmentation contractions in the small
intestine is determined by the frequency of electrical slow waves
Maximum frequency is present in duodenum and proximal jejunum is
(12/min) In terminal ileum it is 8 to 9/min
6. The segmentation contractions become exceedingly weak when the
excitatory activity of the enteric nervous
system is blocked by the drug atropine.
even though it is the slow waves in the smooth muscle itself that cause
the segmentation contractions, these contractions are not effective
without background excitation mainly from the myenteric nerve plexus.
7.
8. Propulsive Movements
Peristalsis in the Small intestine
Chyme is propelled through the small intestine by peristaltic waves.
These can occur in any part of the small intestine
they move toward the anus at a velocity of 0.5 to 2.0 cm/ sec,
faster in the proximal intestine and slower in the terminal
intestine.
They are normally weak and usually die out after traveling only 3 to 5
centimeters, rarely farther than 10 centimeters,
so forward movement of the chyme is very slow, so slow that net
movement along the small intestine normally averages only 1 cm/min.
This means that 3 to 5 hours are required for passage of chyme from
the pylorus to the ileocecal valve.
9. Control of Peristalsis by Nervous and Hormonal Signals.
Control of Peristalsis of Small Intestine Nervous Factors
1. Entry of meal in duodenum
• Stretch
2. Gastroenteric reflex
• Distension of stomach
• Myenteric plexus
11. The ileocecal valve is a sphincter muscle situated at the
junction of the ileum (last portion of your small intestine) and
the colon (first portion of your large intestine). Its function is
to allow digested food materials to pass from the small intestine
into your large intestine.
12. On reaching the ileocecal valve, the chyme issometimes blocked for several
hours until the person eats another meal; at that time, a gastroileal reflex
intensifies peristalsis in the ileum and forces the remaining chyme through the
ileocecal valve into the cecum of the large intestine.
13. Peristaltic Rush.
Although peristalsis in the small intestine is normally weak, intense
irritation of the intestinal mucosa, as occurs in some severe cases of
infectious diarrhea, can cause both powerful and rapid peristalsis,
called the peristaltic rush
This is initiated partly by nervous reflexes that involve the autonomic
nervous system and brain stem and partly by intrinsic enhancement of
the myenteric plexus reflexes within the gut wall itself.
The powerful peristaltic contractions travel long distances in the small
intestine within minutes, sweeping the contents of the intestine into the
colon and thereby relieving the small intestine of irritative chyme and
excessive
distention.