Exam 2 Circulatory & Digestive Systems PDF

Summary

This document covers the circulatory and digestive systems, including details on different types of circulatory systems, the heart, blood vessels, microcirculation, oxygen transport, and the cardiac cycle. It also discusses the digestive system, various food types, and their building blocks. Examples of important biological processes, such as cellular operations and the nervous system, are detailed.

Full Transcript

# Exam 2 ## Circulatory System - **No circulatory:** aquatic invertebrates - **Closed:** vertebrates - Cephalopod annelids - **Diffusion through skin** - **Heart contractions** - **High blood pressure drives fluid movement** - **Muscular pump** - **Vessels connected** ## Systematic Heart - B...

# Exam 2 ## Circulatory System - **No circulatory:** aquatic invertebrates - **Closed:** vertebrates - Cephalopod annelids - **Diffusion through skin** - **Heart contractions** - **High blood pressure drives fluid movement** - **Muscular pump** - **Vessels connected** ## Systematic Heart - Blood to body tissue - Branchial heart → blood to lungs ## Arteries - Blood to heart - Blood away from heart ## Veins - **Difference:** - **Artery:** thicker endothelium, has elastic fibers (bc ABP), smoother - **Small vein:** valve (unidirectional flow) - Cells connected are thin for gas exchange ## Open - No blood vessels - Pumps into hemocoel (unoxygenated) - Sends blood to tissues, open space, bathes ## Vessel Dilation - Controlled by ANS - Changes lumen size, changes blood flow in areas - **(Vaso)constriction:** reduces blood flow - **Dilation:** increases blood flow ## Microcirculation - Through capillaries (vessel walls) - basal lamina/endothelium - **Supply:** - Changes amount of blood - WBCs, hormones, waste, nutrients - Thermoregulation, BP - Must carry blood - **Diffusion** - **Super small - susceptible to BP changes - bad when sick** - **Can obstruct blood flow** ## Oxygen Unloading - Hemoglobin releases oxygen around tissues w/ low O<sub>2</sub> partial pressure - Increases release as need increases ## Cardiac Cycle - Ventricles fill w/ blood - Atria contract (at end of ventricular diastole) - completes ventricular filling - Ventricles contract, atrioventricular close - pressure builds until aortic & pulmonary open - Blood pumped out of ventricles into aorta & pulmonary arteries - Ventricles relax, pressure in ventricles, pressure in aorta/pulmonary - So they close ## Series Circulatory Plan - **2-Chambered** - Gills → heart → systematic tissues - Oxygenated - **4-Chambered** - Lungs → left side of heart → systematic tissues - Right side of heart → right side - Right side moves deoxy to lungs - left side systematic tissues → right side - Unoxygenated ## Digestive System - Ingesting small organisms - **Suspension feeding:** brought into organism - broken down & digested - **Symbiosis:** food obtained from microbial symbionts - **Bulk feeder:** whole animal/chunks - **Deposit:** pick up food waste (worms) ## Foods w/ Building Blocks - **Calcium:** skeleton - **Amino acids:** proteins, energy - **Fatty acids:** membranes, energy - **Nucleic acids:** break chem bonds ## Essential Nutrients - **Calcium** - **Phosphorus:** ATP, nucleic acid formation, bone - **Sodium:** H<sub>2</sub>O balance, nervous & muscular function - **Potassium:** nervous & muscular function - Shifts w/ exercise ## BMR - Resting metabolic rate ## Macromolecules: Carbohydrates ## Proteins ## Fatty Lipids ## Nucleic ## Metabolic Rate - ↑ = more food consumption - Higher aerobic respiration = + BMR - **Birds:** large initial investment, & speed = ↑ energy - **Smaller animals:** need more food/gram of body weight - BMR lowest in big animals ## Division of Labor - Cells specialized for particular function ## Tissue - Similar Cells ## Organ - Or more tissues - defined func. ## Simple Epithelium - One-celled thin sheet - Enables solute movement - Lines digestive tract, absorbs nutrients to produces digestive enzymes ## Size of Epithelial Lining Lumen - Bigger = more flow, digestion/absorption ## Midgut - Gets partially digested food, receives enzymes continues digestion ## Peristalsis - Movement of tract to propel food thru ## Circulatory System Delivers - Nutrients to systematic tissues ## Herbivores - Long intestine for storage ## Vertebrates - Short intestine ## Gizzard - Less developed organisms, breaks up food ## Crop/Stomach - Digest & store - No vertebrae has enzymes to digest cellulose - Have microbes to ## Glucose Homeostasis - Alpha cells - glucagon - Beta cells - insulin - Negative feedback ## Neurons/Action Potential - **Nervous system** - **NS functions:** - **Sensory input:** receptors - **Integration:** thoughts, decisions, memories, sensations - **Motor output:** effector organs (activates via stimulation) - **Neuron structure:** - **Cell body:** organelles - **Dendrites:** receptive - **Axon:** variable size - **Axon terminals:** surface area - If dendrite gets strong enough excitement = generates action potential - **Axon terminals:** - Store neurotransmitters (in synaptic vesicles) - Vary in # - Are excitable - allow release - **Synaptic gap:** neurotransmitters diffuse across to reach excite ## Resting Membrane Potential - Ions - unevenly placed - separated by gradients - More K on inside than Na, vice versa for outside - Requires energy to separate (voltage) - Voltage determines open/close of channels - Ions flow down gradients, $ creates a current - Current → flow of ions, release of potential energy ## Na+ into cell = depolarized, Excited - K+ higher inside, high low (down gradient) - Nat high outside - **RMP:** negative potential? - 1. Na+ K+ pump - 3 Na+ enter - from inside - Releases Na outside - Energy comes, changes pump to open out - 2 K+ enter, Pi leaves & channel changes to open - Inside, K+ released inside (more K+ inside) - 2. Permeability - Leaky channels - allow ions to go where they want - K+ has most leak channels - always changing to - K+ goes outside (high low conc.) - Looses more K+, looses + charge = negative potential ## Member Gated Channels - **Ligand:** chemical messenger binds & opens gate - **Voltage:** current opens pumps/gate → AP ## Neurotransmitters = Lagand - **Na:** has activation gate - At rest this blocks channel, voltage unlocks - Inactivation gate - slowly closes, blocks channel. - Then switches so active is closed & inactive is open, cycle repeats. ## Charges Vary by Strength ## Graded Potentials - Generated by ligand-gated (stimulus) - Neurochemical messenger binds to (stimulus) - Gate opens it by other neuron - Na+ goes down gradient (in), looses - Strength, gets weaker as it moves - Fizzles out, needs enough to reach axon - (Multiple can happen at once) → creates AP ## Membrane Potential - All or Nothing - Changes → signals - **1. Grade:** activates action potential - **2. Action potential:** - Long distance signaling - Constant strength ## Action Potential - **Summation potential:** all graded - Lo if strong enough: changes in membrane potential - Doesn't weaken w/ distance - **1. Resting state** - **2. Depolarization:** makes more positive - All VG Na+ (channels) open - **3. Repolarization:** - VG Na+ channels inactivated - VG K+ channels open - flow out - **4. Hyperpolarization:** - K+ open longer than needed - Then Na+ K+ rest ## AP Propagation - **Myelinated fibers:** prevent Na+ from leaking - Separates ionic attraction across membrane - More gial = higher transduction - faster AP. - Increases conduction velocity - **Ca reacts w/ synaptic vesicles:** releases & diffuses into target cell ## Sensory Systems - Receptor cells transform stimuli into electric signals - **Transduction:** - Conversion of energy to one form or another - **Receptor cells:** - **1. Graded potential (receptor potential):** - Stimulated by light (into chemical energy) - Transduction - **2. Transmission** - Energy relayed to integrative parts of NS (brain, ganglia) - **Sensory receptors:** - More SA = more receptors/sensations - In/directly generates graded (receptor) potential - Different sensory proteins: - **1. Ionotropic:** receptor protein is ion channel - **2. Metabotropic:** receptor protein relays - Signal thru a protein to a channel - (A protein activates 2ndary & than open's) ## Stimulus Detection - Signals relayed to appropriate processing region - Neurons extend from receptor to processing ## Muscle Stretch - **Stretch receptors:** mechanoreceptors - Usually ionotropic - **Muscle spindles:** detect lengthening - Neurons transmit AP to NS. - Frequency dependent on degree of stretch. - Stimulates motor neurons to increase muscle contraction ## Olfaction - Metabotrophic receptor - **Odorants:** chemicals that can cause olfactory response - **Chemoreceptors:** - **Olfactory epithelium:** nasal cavity - mucus coated - Mucus surrounds dendrites - traps receptors - affects other chemicals - AP to olfactory bulb → olfactory nerve → brain ## Auditory - **Mechanoreceptors:** - **Sound waves → electric signals** - **Hearing organ:** thin membrane - makes w/ sound - High frequency = high pitch - Different pitches move diff points of basilar membrane to make - **Organ of Corti:** - Hair cells w/ sterocillia - move = neurotransmitters released - APA - AP → Cochlear nerve → brain ## Vision - **Photoreceptors:** sensitive to light - hyperpolarize neurons - **Opsin:** absorbs light (11-cis-retinal) - vitamin A - Opsin absorbs light → changes shape → activates G-protein → graded potential - Signal processing: light absorbed → cornea → pupil → lens → retina absorbs → processed by integrating neurons → goes to ganglion, AP axons send to brain - **Photoreceptors:** - **Rods:** light - **Cones:** color ## Humans can't use: - Electromagnetic wavelength 400-700 nm - Electric fields ## Nervous Systems - **Functions, neurons, organs, structures:** - **Centralization:** nerves cluster together to form CNS - **Cephalization:** sensory organs congregate at anterior → creates head region - **Evolution:** many sensory organs anterior, coordinated responses - **Neuron classes:** - **Sensory/afferent:** - **Interneurons:** receives & relays to motor - **Motor/efferent:** sends to structure - **Nerve net:** - Dorsal axons → brain, spinal, nerves - Simple NS → brain, ganglia - **Peripheral NS:** - **Afferent:** receives sensory - **Somatic:** Skin, skeletal muscles, joints - **Visceral** - **Efferent:** motor - activates muscles/glands - **Somatic system:** - Motor nerve fibers - Voluntary - **Autonomic:** - Smooth muscle, heart rate - Endocrine glands - Involuntary - Reproductive organs - **ANS (autonomic):** dilation of vessels - **Sympathic:** alertness, heart rate, BP - Exercise, stress, anger, fight or flight - **Parasympathic:** reduced energy usage RELAXES - Body maintenance, waste removal - Digestion - **Enteric:** digestive tract ## Neurons: - Sensory, motor, interneurons - **Polysynaptic:** multiple synapses - 1. Receptor - 2. Sensory neuron - 3. Integration center - 4. Motor neuron - 5. Effector response (goes to inter neuron) - **Monosynaptic:** - 1 synapse between - Motor & sensory - No interneuron ## Muscular System - **Sacromere:** makes contractions) - **Structures:** - Multinucleate - T-tubules - Sarcoplasmic reticulum - stores calcium - Myoglobin - transports O<sub>2</sub>, stores some for when needed - Glycosomes - stored energy, packets of glucose chains - Can break down & use ## Sarcomere - **Sz time** - Contains: **Actin (thin)** & **Myosin (thick)** - **Titin:** anchors myosin, elastic, connects to ends of thick - Pulls inward (shortens) when contacted. - **Excitation:** muscle cell excited AP generated - **Contraction:** electrical excitation leads to contraction - Coordinated by neuron ## Contractions - **1. Motor neuron stimulates AP** goes to axon terminal to **make vesicles** - **Vesicles released** & **diffuse** across synaptic gap - **Ach binds to channels** for Na+ to flow in (not at rest) - Ach **positives electric current** → **excites** (electrical signal) - **AP signal spreads:** spreads across membrane - **T-tubule allows travel** of AP deep into cell - **T-tubule protein excited** by AP, **releases Ca**, opens **channels for Ca to go into cytoplasm** ## Reflex Arc - Neurones: sensory, motor, interneurons - **Polysynaptic:** multiple synapses - 1. Receptor - 2. Sensory neuron - 3. Integration center (goes to inter neuron) - 4. Motor neuron (longer) - 5. Effector response - **Monosynaptic:** - 1 synapse between - Motor & sensory - No interneuron ## Muscular System - **Sacromere:** makes contractions) - Structures: - Multinucleate - T-tubules - Sarcoplasmic reticulum - stores calcium - Myoglobin - transports O<sub>2</sub>, stores some for when needed - Glycosomes - stored energy, packets of glucose chains - Can break down & use - **Sz time** - Contains: **Actin (thin)** & **Myosin (thick)** - **Titin:** anchors myosin, elastic, connects to ends of thick - Pulls inward (shortens) when contacted. - **Excitation:** muscle cell excited AP generated - **Contraction:** electrical excitation leads to contraction - Coordinated by neuron ## Contractions - **1. Motor neuron stimulates AP** goes to axon terminal to **make vesicles** - **Vesicles released** & **diffuse** across synaptic gap - **Ach binds to channels** for Na+ to flow in (not at rest) - Ach **positives electric current** → **excites** (electrical signal) - **AP signal spreads:** spreads across membrane - **T-tubule allows travel** of AP deep into cell - **T-tubule protein excited** by AP, **releases Ca**, opens **channels for Ca to go into cytoplasm** ## Check Book Marks ## Muscle Contraction - **Sliding filament:** - **Thick filaments** attach & pull **thin** (myosin) - To center - **1. Ca2+ released** by sarcoplasmic membrane - **2. Ca2+ binds to troponin** - changes shape - **Troponin untwists tropomyosin** - uncovers myosin binding sites - Allows cross bridge cycle - **Muscle contraction:** - **Cross bridge:** underlies sliding - Makes bond possible - **1. ATP binds to myosin** (myosin = low energy now) - **2. ATP hydrolysis** → ADP+Pi - **Myosin now activated conformation** (can bind to filament) - **3. Myosin binds to active site (cross bridge)** - **4. ADP+Pi removed, myosin changes** - Creates power stroke → **puts sacromere to middle, removes Pi** - **Shoots forward (squooshes along)** toward M-line - **Lo restarts cycle to end:** - **1. Neuron stops communicating w/ muscle cell** - **2. Ca2+ transported into SR** - **3. Troponin retwist tropomyosin** (hides bonding heads) - **4. Creates resting conformation** ## Exoskeleton - Pulls on interior surface - **Apodeme:** projects into body, muscles attach here - **Catch muscle:** structure closer to main body ## Hydrostatic Skeleton - Uses fluid from body cavity to move - **2 layers of muscle** - Contract at diff times to slide ## Contraction ATP - **Need for:** - Cross bridge movement - K+ & Na+ pump - Regulates charge - **Production:** - **Immediate:** creatine phosphate stored, when bond broken = ATP - **Glycolytic:** glycosis CC-30 - **Oxidative:** not sustained ## Skeletal Fiber Types - **Slow oxidative:** marathon, resist high endurance, thin - **Fast oxidative:** relay, moderate exercise, thick ## Fast Glycolytic - Powerlifting, sprinting, intense/powerful movements, few capillaries ## Endurance - Fast glycolytic/oxidative ## Skeletal System - **Endoskeleton:** bone, cartilage, bone cartilage bank - regulate calcium - **Exoskeleton:** - **Molting:** allows growth for exoskeleton - Vulnerable during molting ## Bone Cells - **Osteoblasts:** deposit new bone - **Osteocytes:** osteoblasts surrounded by bone - **Osteoclasts:** dissolve bone - Ca to ECF ## Bone - **Membranous:** forms on CT membrane - **Cartilage:** first cartilage thin, ossifies to bones - **Compact** - **Cancellous** - **Holes** - **Haversian canal** - for blood vessels - **Spongey** - no haversian ## Innate Immunity - **Innate:** - Genetically programmed - Nonspecific - *First line of defense* - Physical barriers, toxic molecules - Relatively quick response - **Inflammation** - Protection againts pathogens - **1. Recognition phase:** recognize pathogen - **2. Activation phase:** mobilization of cells/molecules to help - **3. Effector phase:** invader is destroyed - **Physical/chemical barriers:** - Thick epithelial - Sweat - can deter bacterial pathogens - **Amoebocytes:** cells for pathogen destroying - **Adaptive:** - Targets specific pathogens - Antibodies made - Slow, long lived - Evolved in vertebrates - Creates memory ## Innate Defenses - **Toll-like receptors:** - Mostly active during recognition/activation - Participate in innate defense (type of PRR) - **Vertebrates:** TLR binds to FER bacteria (recognition) - Protein kinase cascade - one activates another until defensive protein TF - Transcription factor changes - TF enters nucleus & binds to promoters - Genes encoding defensive proteins are created. - **Cell types WBC:** - **WBC/leukocytes:** - Large cells, ingest pathogens - Phagocytosis - adaptive/innate immunity → TB cells ## WBC = 2nd Line of Defense - **Basophiles** - release histamine & inflammation - **Eosinophiles** - kill antibody coded parasites - When WBC are activated (pathogen gets close to blood) ## Mammalian Defense - Lymphatic System - Lymphoid tissues - Blood plasma - Lymph - fluid derived - Fluid pushed out of capillaries bc of pressure - When leaving usually blood takes back up - Lymph nodes - have dead ends, circulate up to heart & then transports - Have dead ends, WBCs to detect pathogens & respond. ## First Line of Defense - External surfaces: PA, skin - Mucus membranes (secrete mucus) - **Defensins:** protein/peptide insert into pathogen cell - kills cell by disrupting gradient - Toxic to bacteria - Doesn't kill our own ## Bad Line - Activate WBCs. - **TLR is PRR.** - **TLR binds to PAMP:** recognizes PAMPS - Creates downstream signal transduction pathway - PAMP allows defense ## Inflammation - To isolate area & recruit WBCs P responders - **Helper responders:** - **Tumor necrosis factor** - **Prostaglandins:** help initiation of inflammatory response - **Histamine:** increases blood vessel permeability - More WBCs & molecules - **1. Damaged tissue recruits histamine (for diffusion) - Vessels** become leaky & dilated - **Blood plasma & phagocytes** move to infected tissues via vessels - **Phagocytes engulf bacteria** - **Histamine & signaling stop** - no more calling phagocytes - **Heal w/ WBCs** ## Humoral Immunity - **INNATE(complement)** - **EXTRA-cellular** - Antibodies specific to pathogen - B-cell circulate - **Natural active:** produce antibody, natural exposure - **Artificial active:** production of antibody via VACCINE - **Natural passive:** temporary immunity, antibodies from other person - **Artificial passive:** temporary, injection of immune serum - **Adaptive:** - **Specificity:** - **Diversity (lymphocytes):** memory - **Distinguish between self & itself** ## Specificity - **B cells:** produce antibodies (free-floating antigen binding) - **T cells:** B lymphocytes - WBCs, produce antibodies - **Antigenic determinants:** pattern on antigen immune system recognizes - **B-cell activated** by TH - **Binds to antigen binding site** (one open for B cell, another for antigen) - **B-cell receptor** ## Memory - **1. Primary immune response:** antibody & T-cell production - **2. Secondary immune response:** rapid response - Infection w/ previously encountered pathogen ## Memory - 1. Recognition - B-cell makes antibody to bind to antigen - 2. Activation - T-cell stimulates B-cell to divide a bunch - 3. Primary response - some time cells become plasma cells (effector) - Secrete sine antibody as parent cell - Potentially cells develop into non-secreting memory cells - Divide at slow rate, keeps a clone ## Recombination - Takes any combination of segments from a gene - Shown on mRNA & allows for recombination. - To get antibodies - Takes immunoglobulin genes ## Antibodies - **Con:** - **1. Activate Compliment System** - Antibodies become activated when binding antigens to pathogen surfaces. - Activates complement proteins. - Creates protein structure to attack & lyse a cell - All coded in antibodies. - **2. Activation of effector cells** - Attracts NK, phagocytes - Helps neutralize antigen ## 1. Humoral, Innate - Enhances phagocytes to clear microbes/damaged cells - **Func: inflammation:** - Cell membrane attack - Phagocytosis ## Pathway - **1. C-protein binds to pathogen (C3b)** - Phagocyte recognition - **2. A diff C-protein activates inflammation (C3b)** - Phagocytes attracted - **3. C-protein inserts in pathogen menibrane** - Creates holes & dies ## Adaptive - **Cell-Mediated Immunity** - Requires cell contact (for diffusion) - **T-cell:** - T-lymphocytes/T-cells - **T-cells have surface receptors** (like B-cells) - **T-cell receptors:** - Not immunoglobulins but glycoproteins - Similar to B: - Alpha chain - Beta chain - extends throughout membrane - **Constant region** & **variable region** - Only binds to **antigens when bound to MHC protein** ## MHC Proteins - **TH:** - T-helper cells - activates adaptive immune response - **TC:** - T-cytotoxic cells - death of all displaying antigen - **Which T-cell?** - **MHC Class 1:** present on surface of all nucleated cells (nonspecific) - Display antigens/viral proteins stuck to MHC then T-cell - If replicated, as binding to APC release/perforin - Lyses cells - **MHC Class 2:** on B-cell surface, macrophages, dendritic cells - Present antigens to TH cells - **1. APC takes up antigen** via phagocytosis - **2. Cell breaks antigen** into fragments. - **3. Class 11 MHC protein** binds to antigen fragment - **4. MHC presents antigen** to TH - **More TH created** and all **release cyotkins:** - Communication w/ other cells - Stimulates: - NK - Macrophages - B-cells - **Myosin = thick** ## Regulatory T-cells - **Tregs** - Have special receptor - Helps determine self/nonself - Mediates tolerance to self antigens - Binds to self-antigens to tell TH or TC to not kill self - All, kill TC/TY instead on APC - **Recognize nonself antigens** - **HIV is symptoms of AIDs** ## AIDS - Kills TC/infects TH - Activates TH, infects TH & dying - TC kills TH (cause TH infected) - TH infected exponentially - Virus attacked, HIV +, low level remains TH is going down - Dormant stage - low TH levels - no tell to help, low virus levels - virus grows again ## Endocrine - **Why NS & endo?** - **NS:** fast, can end abruptly - Targets body region, uses neurons to signal - **Endo:** slow, broadcast, slower to end - Targets specific kinds of cells - More efficient - Uses hormones to signal ## NS & Endo Work Together to Maintain: - Homeostasis - Coordination - Response to signals ## Extra - **Ficks law:** rate of diffusion/ SA - Rate of diffusion is proportional to SA - Doesn't apply between gas mixture & aqueous. - **Endocrine system:** - **Autocrine signaling:** acts on signaling cell - **Paracrine signaling:** acts on nearby cells - **Endocrine signaling:** use circulatory system to transport ligands - **Pheromone:** chemicals that trigger behavioral response ## Endocrine Glands - Secretes into blood stream - No ducts - Intracellular affects (changes internal physiology) - High capillary density - Fenestrated (has holes for hormones to diffuse) - Cell to cell communication ## Exocrine Glands - **Ducts:** - Secretes onto epithelial surfaces (straight onto glands) - Extracellular effects (digestion) - Goes to all kinds of glands ## Endocrine Cells - Neurosecretory - behave like neurons, release hormone (not NT) - **Neurohemal organ:** neurons next to - Creates AP, from axon terminal - AP allows secretion into capillaries & then target cells - **Non-neural endocrine cells:** epithelial endocrine cells - All secretes directly into capillary ## Hormone Classes - **4-rings Steriods:** made from cholesterol - **Monoamines:** made from 1 or 2 AA (dopamine, adrenaline, TH) - **Linearish Peptides:** 3-200+ AA → hypothalamus inhibitors. - **Transport:** - **Monoamines/peptides:** diffuse directly across, travels through blood - **Steriods/TH:** uses transport proteins to circulate through blood - Creates stability & increases half-life ## Steriods - Hydrophobic - Can diffuse through membrane - Gene activation - Most go straight to nucleus - To find hormone receptor - **1. Find receptor** - **2. Stimulate mRNA** - **3. Transcribe new protein** - **4. Protein releases effects** ## Peptides - Hydrophobic - Cannot diffuse through membrane - Receptor on cell surface - Travels freely - Much faster - Uses air made proteins - **1. Hormone receptor** activates G-protein - **2. Activates adenylate cyclase** - **3. Adenylate cyclase make cAMP (from ATP)** - **4. cAMP activates protein kinase** - **5. Protein kinase phosphorylates enzymes** - Activates or deactivates - **6. Activated enzymes** catalyze metabolic reactions = wide range of effects. ## Target cells - Function can change over time - Function can be different in individuals - Certain receptors determine for different hormones on target cells. - Diff cells have diff receptors, leading to varied cellular responses when bound ## Hormone Release - **Peptides/AA:** fast, stored in vesicles - **Steriods:** slow, most synthesize - Transport protein ## Hormone Removal - **Target cells can degrade** - **Half-life** - **Liver/Kidney can degrade** - **Can be excreted** ## Portal System - Veins Start & End In Capillaries - One bed to another ## No Major Endocrine Control - **Hypothalamus:** - Involuntary - neurosecretory - Hunger, thirst, sex drive, stress response - **Pituitary:** - Connected to hypothalamus - Infundibulum - Connects hypo & pituitary ## Anterior Pituitary - **Circulatory Connection** to hypothalamus - Neurosecretory neurons. - Capillaries only in infundibulum, communication between neurons & neurosecretory. - Flow: neurosecretory from hypo secretes in 1st capillary bed, moves to 2nd capillary bed - **Hypophyseal Portal System** - Anterior has endocrine cells - If receptor present, then secretes into blood to find target cells ## Control: Hypothalamus Signaling - **Release hormones:** travel from hypo to tell pit to release - **Inhibiting hormone:** silence target cells in pituitary (doesn't release) - **Stimulation** in waves - **Tropins:** control other glands endocrine glands - **Hormones:** ACTH, TSH, FSH, LH - **Act on non-endocrine:** GH (growth hormone) PRL (prolactin) ## Posterior Pituitary - **Made of nervous tissue, not a true gland** - **Neuroendocrine cells** - Neurosecretory cells in hypo have axons extending to posterior - Axon is transporter (not blood) - Hormones stored in nerve endings - When stimulated, releases - **Hormones:** ADH, Oxytocin ## Negative Feedback - **Hypothalamus:** - GnRH - CRH/FSH - Thyroid → - **Ant:** - GH - ACTH - Cortisol ## Gland - **Pineal gland:** melatonin, sleep cycle - **Hypothalamus** - **Thyroid** - **Parathyroid:** 4 parathyroid - **Thymus:** T-cell - **Adrenal cortex** - **Pancreas** ## TH Helps w/ Bone Regulation ## Thyroid Gland - Endocrine gland - vascular tissue for transportations - **Brain regulates BMR:** - TRH released by hypothalamus → anterior TSH → thyroid TH - ↓ reduces BMR - **More TH = more slowed down BMR** - **Follicles:** follicular cells - Filled w/ colloid - Secretes TH - Regulates BMR - Single larger of cells - **Receives TSH:** stimulates release of TH - Before release: - 1. Stimulate follicular - 2. Take in colloid - 3. Chop colloid into 2 AA - If 3 iodines attached = T3 ## Colloid: Storage - Contains T<sub>4</sub> & iodine ## Parafollicular Endocrine Cells - Secretes calcitonin (increases bone formation) ## Disorders: Hypothyroidism - **Goiter:** super inflamed lymph node - Usually by: - No iodine - No TH - More TSH = more TG - No iodine → no TH → more TSH → overstimulation of follicular - More storage space - Colloid increases # Insect Development - Development in steps - Growth by molting, shape change ## Development Hormones: - **1. PPTIH:** prothoracicotropic hormone - Stored in neurosecretory cells - Target prothoracic glands - Allows ecdysone release - **2. Ecdysone:** - Protein that allows exoskeleton molting - Loosen connection/adhesion - **3. Juvenile hormone (JH):** - Non-neural cells (steroids) - Released at each molting - Decreases w/ molting, most mature stage after no JH - Allows pupa (resting state) - Becomes adult ## PPTH Stays Constant ## JH Decrease ## Interneurons - Bridge between sensing & motor ## Sacromere - **Actin:** thin filament - **Myosin:** thick - **Z-line:** separation between sacromeres (constant) - **A-band:** thick filaments (stays constant) - **H-zone:** only thick - **I-band:** thin filaments only - **M-line:** center of sacromere # Where Murin Meets Muscle Fibers - Fluid w/ Ach - That breaks down Ach (stops continuous stimulation - Into synaptic cleft (initiates impulse) - To end plate - Ach finds receptors - Sarcolemma, goes down T-tubules - Sarcoplasmic reticulum to release calcium - Calcium, myosin head binding, activates - Mylion (cluster outside of CNS) - Muscle/gland ## Produces Interferons - **Interferon recognition & response**

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