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All about Physiology in paragraph form
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acid transmitters stimulate positive responses in post synaptic cell. They are modifications to readily available molecules to alter. They go from stimulatory to inhibitory such as stimulatory glutamine to gamma buric acid (GABA). Neuropeptides are small peptides that are stored in the synaptic vesicles Catecholamines start at tyrosine to L-dopa to dopamine to norepinephrine to epinephrine Mono amines are serotonin and histamine Neuromodulators are long time changes to neuroactivity such as learning. Neuromodulators change function of neurons by modifying activity within it by changing the products inside the cell. Neuroeffector communication gets immediate results through changing membrane voltage. By changing permeability. For example, bind to the channel pore so neurotransmitter opens pore and ions pass without fureewnt flow. Once action potential gets to axon terminal, calcium is responsible for snare proteins and neurotransmitters to diffuse thru the synaptic cleft and bind to the receptor which then changes the membrane voltage or we could use a second messenger system that could open the calcium channel by binding to some receptor on receptor origin to geta response Snare proteins are group of proteins that will cause synaptic vessels to move along the presynaptic projection to release a neurotransmitter to the synaptic cleft Receptors initiate any nervous activity and are sensitive to stimulus energy. Receptors let us know when something Is changing, nothing can occur if the receptor isn’t activated because they transfer energy into electrical energy of nervous system. Receptors work thru graded potential meaning a change in permeability means depolarize and release of ions to reach threshold and fire an action potential. They are influenced by the intensity of the stimulus, the rate of change of stimulus activity and summation for example spatial summation receptors increase information of stimulus Doctrine of specific nerve energies is design receptor to pick up particular types of energies to then perceive anything in that pathway as that specific energy Hormonal control The endocrine and nervous system regulate the body. Hormones change activity of target cells. Hormones can also be released in one part and stimulate another part. One characteristic about hormones is that they use blood instead of physical connection to get to its destination. The target will have receptors related to the hormone to not activate nontarget cells. Endocrine glands produce more than one hormone and can produce the same hormone in different places. The gland gets stimulation to release the hormone in the plasma. Hormones can be synthesized in 3 general classes: amine, thyroid and steroid hormones. Amine hormones are all derived from tyrosine can are subdivided into thyroid and adrenal medulla hormones. T can be stored as thyroglobulin when there is iodine and released by thyroid gland to convert to T3 before it becomes active. Thyroid can regulate metabolism and determine the BMR. Adrenal medulla hormones produce catecholamines and releases norepinephrine and epinephrine. Peptide hormones are synthesized from large precoruirse molecule. Peptide hormones depend on the receptor at the target tissue to determine what the activation pathway will be. Steroid hormones found in the adrenal cortex and gonads are built on cholesterol. Depending on which steroid you produce, that will determine on which enzyme is present. It begins as a cholesterol then gets modified on the enzyme present. The principle of complementarity says what you produce is based on the enzyme present in cells. Steroid hormones can be divided into adrenal cortex hormones and gonadal hormones. Adrenal cortex hormones are made up of the zona glomeerlosa, zona fasciculata, and zona reticularris from superficial to deep. Zona glomera makes mineralocorticoids and aldosterone, zona reticularis is made up of interconnecting layer of cells that form reticulated pattern. It specializes in using androgens such as androstenedione and dehydroepiandrosterone and not testosterone. Adrenal medulla hormones start with tyrosine to levodopa to dopamine then finally norepinephrine and epinephrine. Peptide hormones start with mRna in ribosome to preprohormone in the ER to the prohormone in the golgi then finally producing a hormone Gonadal hormones will produce testorone or estradiol
Steroid and thyroid hormones are lipid soluble so they bind to proteins that act as transport proteins. Free hormone and bound hormone determine the total concentration of hormone in solution. Only free hormones can interact with receptors and get a response. Steroid hormones and T4 can diffuse thru the cell membrane if there is a cytoplasmic or nuclear receptor for a particular hormone. If cytoplasmic, they bind to the cytoplasmic receptor to the hormone receptor to work its way to the nucleus. If nuclear, it just binds to the DNA hence already inside the nucleus. Catecholamines and peptide hormones change activity of the cell through second messager systems while steroid and thyroid hormones change the acitiy of the genome itself Rate of metabolism and excretion is dependent on how strong of a bond is with the transport molecule and how many are present. If hormones are bonded to transport protein the half-life is increased There are three ways to activate hormones. First by activating the target cell directly, or activating another form of the molecule to activate target cell such as releasingT4 because of its longer half-life and once its dissolved thru the membrane, T will be activated which can then bind to the receptor and get a response. Finally, we can activate other molecules How much hormone in the blood is determined by how much is secreted – excreted – amount of inactivated. If we secrete more the excretion stays the same and the concentration increases. If we decrease secretion everything else decreases. Activation of target cell Hormones whom can’t pass the cell membrane because they are not water soluble bind to a membrane bound receptor on the cell surface to trippeer a second messager system such as cyclic AMP Permissive effect is when one hormone will increase the effectiveness of another hormone. For example, FSH and estrogen have effect on LH to cause ovulation Inputs controlling hormone secretion Any gland can be influenced depending on the concentration of organic nutrients, neuronal control and hormonal control. For example, Insulin serving as a hormone will release when glucoses’ an organic nutrient, concentrations increase to let insulin penetrate the cell. Neuronal control will stimulate the release of hormone by activating the gland with the synapse Hormonal control is when the hormone regulates the release of another hormone, also named tropic hormones. Tropic hormones stimulate target to releasee another hormone Hypothalamus and pituitary control systems In the hypothalamus the supraoptic and paraventricular nucleus which will make antidiuretic hormone and oxytocin to send those hormones through the hypothalamic physio tract down to the neurohypophysis to then release the ADH and oxytocin. The ADH goes to the kidneys and causes reabsorption of water. Oxytocin will stimulate smooth muscle concentration. pituitary control system secretes 6 hormones The hypothalamus is the master endocrine system as it has a releasing and inhibiting factors for the hormones. It is made up of 2 groups of nuclei: supraoptic and paraventricular nucleus. Supraoptic nucleus produces antidiuretic hormone also known as vasopressin (suppressing urine). The paraventricular nucleus makes oxytocin. These two hormones work with the hypothalamic tract to the infundibulum in the cela turcica to the neurohypophysis to the pitatry to then produce ADH or oxytocin For the hypothalamus to communicatee with adenohypophysis they have to use the blood thru a special circulation called the pysioportal system to then two capillary networks as the adenohypophysis has a different embryological origin, it is epithelial not neural. There are releasing and inhibiting hormones in the hypothalamus that are then transferred to the hypo physio portal system to the adenohypophysis.