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An in-depth exploration of anatomical positions, languages, body cavities, and regions. It covers topics such as the human body's divisions, the thoracic and abdominal cavities, and the functions of various layers and membranes. Students will also learn about metabolism, homeostasis, and the endocrine system.
Typology: Study notes
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CBIO 2200 Study Guide
1/10/ Anatomy—Study of structure, answers “what is it?” Physiology—Study of function, answers “how does it work?”
Anatomical position: -Erect human body with feet flat on the floor -Palms facing forward/outward with hands down -Eyes facing forward -Arm is supinated (opposite is pronation)
Anatomical Language: Anterior=Front Posterior=Back Ex. Sternum is anterior to vertebral coloumn Superior=Above Inferior=Below Ex. Nose is superior to lips Medial=midline Lateral=away from midline Ex. Ear is lateral to nose (referencing the midline of the human body) Proximal=Near Distal=away Ex. Elbow is proximal to carpal (referencing the limbs to the major limb joints) Ipsilateral=Same side Contralateral=opposite sides Ex. The right ear is Ipsilateral to the right eye
Anatomical Planes: -Transverse Plane—Divides body into upper and lower portions -Coronal/Frontal Plane—Divides body into anterior and posterior portions -Sagittal Plane—Divides body into left and right portions -Midsagittal Plane—Divides straight in the middle at the midline
Dividing Body Regions: -The Abdomen can be divided into 4 quadrants and into 9 regions
Body Cavities
Cavities that are open to the exterior—Nasal, lined with mucous membrane
Cavities that are closed—do not open to the exterior
Anterior Body Cavity -Thoracic Cavity -2 Pleural cavities Houses the Lungs -Cardiac cavities Houses the Heart -Mediastinum Separates the pleural cavities and houses the thymus, trachea, esophagus and the large blood vessels -Abdomincalpelvic cavity -Abdominal cavity Houses the digestive organs -Pelvic cavity Houses urinary organs Posterior Body Cavity (filled with Cerebral Spinal Fluid CSF) -Cranial Cavity Houses the brain There are 3 layers that cover the cavity collective called the 3 meninges -Dura Mater (outer layer)--tough -Arachinoid membrane-looks like a web -Pia Mater (inner layer)--delicate -Vertebral cavity Houses the spinal cord
Anterior Body Cavity Make Up
Ex. What is Visceral Pericardium? Inner layer of the serosa membrane that covers the heart
What is Parietal Pleural? Outer layer of serosa membrane that lines the cavity in which the lungs are located Abdominal Pelvic Cavity Make Up -Housing all of the visceral of abdomen Ex. What is Vsiceral Peritoneum? Inner layer of the serosa membrane that lines the organs of the abdominal region What is Parietal peritoneum? Outer layer of the serosa membrane that lines the cavity in which the organs of the abdominal region are located
Mediastinum The partition that separates the 2 pleural cavities Contains the pericardial cavity, trachea, esophagus, thymus gland Thymus gland -The thymus gland is large in children and starts to shrink at the age of 7 to almost disappearing at the age of 100 -Secretes hormone called Thymosine -Used for maturation and differentiation of your T cells (T-lymphocytes) -Very important in immunity Serosa Membranes and Mesentery Double layers of the peritoneum that covers the abdominal region Posterior Mesentery -Continuation (infolding) of the serosa membrane -Attaches small intestines to posterior body wall Mesocolon -Mesentery that attaches(suspends) the large intestine (colon) Anterior Mesentery (used for organ suspensinon) -Infolding of mesentery turns fatty -Greater Omentum--hanging from the stomach and covering the small intestines -Lesser Omentum—attaches inferior region of liver to stomach Retroperitoneum Space in the abdominal cavity behind/posterior to(retro) the peritoneum. Organs that are retroperitoneal only have peritioneum on their anterior side Ex. Kidneys, Aorta, Pancreas
Metabolism The Sum of energy processes in the body Catabolism -Biochemical reactions that produce energy by degrading large molecules into smaller molecules Ex. Glucose + O2Co2+H2O (Makes 38ATP) Anabolism -Biochemical reactions that use energy to produce larger molecules Ex. Amino Acids +Energy large protein molecules Homeostasis -Homeo= home, stasis=constant
110= hyperglycemia
After a Big Meal Glucose level increases, stimulating the beta cells of the islets of langerhans (pancreas) to secrete Insulin, which reaches the liver. Liver converts glucose to Glycogen in the liver and muscles. Liver acts as a storage site for glucose in the form of glycogen
EatGlucose Increasesbeta cells of pancreas stimulatedsecretes insulininsulin reaches liver liver and muscle converts glucose to glycogenglycogen is stored in liver Insulin lowers Glucose level in Blood
Starvation Glucose levels dropalpha cells are stimulatedwhich secretes GlucagonGlucagon stimulates break down of Glycogen TO Glucose in liver Glucagon increase Glucose level in Blood
The Body Uses Feed Back Mechanism to Maintain Homeostasis
Negative Feed Back T3= Triiodothyronine, T4=Tetraiodothyronine Excess T3 and T4 inhibits the Hypothalamus and Anterior Pituitary TRH=Thyrotropin Releasing Hormone TSH=Thyroid Stimulating Hormone
Positive Feed Back Posterior Pituitary= Storage gland for Oxytocin (nonapeptide) OT=Love bonding hormone, memory, uterus contraction during labor
During labor, Cervis will send nerve impulses to hypothalamus where OT will be further secreted to cause more contractions
You can also get Positive Feed Back involving breast feeding
I. Proteins Amino acids-Building Blocks of Proteins Gly, Ala, Phe(Essential) -Phenylalanine cannot be synthesized on its own, essential amino acid, eat foods with Phe -Phenylalanine Hydroxilase (enzyme) which adds OH to make Tyrosine. -If Phe Hydroxilase does not work, a genetic disorder occurs. -The accumulation of Phenylalanine is converted into Phenyl Ketones instead of Tyrosine -Phenyl Ketones hurt the nervous system causing mental retardation -Recessive Genetic Disorder Produces NON FUNCTIONAL PAH, which causes PKU (PhenylKetonUria) -PKU= Phenylketones appear in urine -Babies with PKU will have strict diet that is almost free of phenylalanine. -Babies still needs small amounts of Phe
Sulfur Containing Amino Acids Cysteine- contributes to the stabilization of proteins using Disulfide Bonds (very strong covalent bonds)
Methionine—First Amino Acid to be assembled in Translation/Protein synthesis which takes place at the ribosome Ex. Met-AA-AA-AA-AA Disulfide bonds form when Sulfur groups are in close proximity
Lysozymes —Enzymatic proteins that have disulfide bonds Used for degrading cell walls of bacteria Present in Lacrimal secretion (tears) and saliva Function: Degradation of bacterial cell wall
Peptide Bonds Forms from dehydration/condensation reactions and produces water Peptides – Made up of Amino acids linked together by peptide bonds (covalent bonds)
Amino Acids
II. Carbohydrates -Macromolecule, complex polysaccharides, complex sugars
Gly(Glycine)
Ala (Alanine)
Phe (Phenylalanine)
Cys (Cysteine)
Met (Methionine)
Tyr (Tyrosine)
Ribose Deoxyribose C5H10O5 C5H11O
How to make Polysaccharides
-Condensation of 2 monosaccharidesDisaccharides
Ex. Glucose + Galactose Lactose (Milk sugar)
Polysaccharides are the most complex sugars which are made up of monosaccharides linked to together by Glycosidic Bonds
Glycoprotein= sugar + protein Ex. TSH = Thyroid Stimulating Hormone TSH reaches the follicular cells of the Thyroid Gland releasing T3 and T4.
III. Lipids Most lipids are made up of structural units called Fatty Acids.
Fatty Acids -Carboxyl group -Long chain of carbon and Hydrogen Fatty acids can be Saturated (no double bonds in tail) or Unsaturated (at least one double bond in tails)
Fatty Acids
Naturally occurring unsaturated FAs can be degraded quickly/easily
Trans FAs are resistant to degradation allowing for longer shelf life, but are not degraded as easily and are not good for health.
Polyunsaturated FAs Ex. Arachidonic Acid = C Common component of phospholipid molecules found in plasma membrane of many cells
Phospholipid Molecules (Amphibolic) Phosphatidylinositol-4,5-Bisphosphate
Contains: -Glycerol Backbone (3 carbon alcohol) -2 Fatty Acid tails -Phosphate group -Polar Molecule There can be Mono, Di, and Tri-glycerides Phosphatidylcholine
Cholesterol It is a steroid Ex. Testosterone, Estrogen, Aldosterone, Vitamin D
IV Nucleic Acids DNA=Deoxyribonucleic Acid (missing – OH at C2) RNA=Ribonucleic Acid Nucleic acids are made up of Nucleotides
Each nucleotide consists of: -Nitrogen Base -Sugar (pentose) -Phosphate group
DNA is linked by Phosphodiester Bonds
Nitrogen Bases A, G, C, T A, G, C, U Sugar Deoxyribose Ribose Role Replication, Transcription Translation Place Nucleus Out of Nucleus using ribosomes
Ex. ATP= Adenosine triphosphate AMP= Adenosine monophosphate UDP= Uridine diphoshphate
Nucleic Acids Nucleotides Nucleosides Nitrogen Bases Many nucleotides linked together by phosphodiester bonds
Nitrogen Base + Sugar+ Phosphate
Nitrogen base + sugar Adenosine Adenine Gaunosine Guanine Cytidine Cytosine Thymidine Thymine Uridine Uracil
The Cell The Cytoskeleton has 3 different fibers Microfilaments, Microtubules, Intermediate Filaments
Cell Structures
Microvillus: Increases absorbing space. “Drinks” for the cell. Cilium: Moves extracellular fluid. Has a 9+2 system. Flagellum: 9+2 system also. o Basal Bodies: 9+0 system, direct formation of microtubules with flagellum and cilia. o Centrioles: 9+0 system, direct formation of microtubules of spindle fibers during cell division Mitochondria: Site for ATP production (cellular respiration), 34 ATP are produced. o Formula: Glucose + O 2 CO 2 + H 2 O 38 ATP Ribosomes: Site for protein synthesis o Transcribed in nucleus Exits through nuclear pores o Translated in ribosomes
Endoplasmic Reticulum (ER): Initial processing of proteins
Golgi Body: Final processing and packaging of proteins
Lysosomes: Contains digestive enzymes
Peroxisomes: Contains catalase
Plasma Membrane: Phospholipid BiLayer
o Glycolipid + Glycoprotein = Glycocalyx Plays a role in cell adhesions and recognition
o Other Functions of Plasma Membrane Proteins: Act as transporters 1.) Channels: Passive transport (no ATP or cellular respiration required) Symport
2.) Pumps: Active transport (Needs ATP or cellular respiration)
Antiport
Transport Across Plasma Membrane
Small molecules/ions
Passive Transport- Does not require ATP
o Filtration-Filters thru pores/slits in plasma membrane Ex: Filtration in kidneys; rate: 180L/day
o Diffusion Simple- Does not require protein carriers Ex: CO 2 -O 2 exchange: O 2 diffuses thru capillary with CO 2 to create a gas exchange (external respiration)
Facilitated- Requires protein carriers Ex: Aquaporin
Active Transport- Requires ATP
o Symport: Glucose-Sodium Channel (secondary active transport) o Antiport: Sodium-Potassium Pump (primary active transport) o Uniport: 1 type of substance transports in 1 direction Ex: Cl-^ pump in trachea Cl-^ is pumped actively Na+^ follows as a result of electrical charge H 2 O molecules follow by osmosis which creates water mucus molecules which allow movement of cilia
Disfunctional Chloride Pump: mucus that is not secreted and builds up. This thick mucus causes infection from the buildup of bacteria accumulated from the mucus. (Cystic Fibrosis Transmembrane Regulator) CFTR
Receptor-Mediated Endocytosis
Coated Pit Coated Vesicle
Familial Hypercholesterolemia (FH) o Genetic disorder of high cholesterol. Disfunctional receptor protein.
Different functions of Plasma Membrane Proteins
o Enzymes: ATPase ex: Na+^ - K+^ pump o Adenylate Cyclase: Converts ATP to cyclic AMP and PPi
ATP (Adenosine TriPhosphate) Cyclic AMP (Acts as 2nd^ messenger) + PPi (Pyrophospate)
Receptors/Recognition sites/Adhesion sites: Glucagon
Events at Neuromuscular Junction
ACh Acetate + Choline (taken by neurons for synthesis of new Ach molecules)
AChE