After our test over the CNS, the lecture consisted of learning about the remaining cranial nerves and then an introduction into the peripheral nervous system. 3 important terms that pertain to our senses include: smell=olfaction, hearing=auditory, taste=gustation. The cranial nerves are ordered by roman numerals from the anterior to the posterior part of the base of the brain. They include: I olfactory, II optic, III oculomotor, IV trochlear, V Trigeminal, VI Abducens, VII Facial, VIII Vestibulocochlear, IX Glossopharyngeal, X Vagus, XI Accessory, XII Hypoglossal. We learnt the entry and exit points of each nerve through the skull, as well as the function of the nerve. It is important to note that sensory nerves are afferent nerves (toward the brain) and motor nerves are efferent (away from the brain). There are also mixed cranial nerves that have sensory, motor, and/or autonomic functions. If cranial nerves are mixed and have autonomic fibers, they are always parasympathetic axons. Our brief introduction to the Autonomic Nervous System described the parts of the neuron that lead from the CNS to the target. (Nerves from the ventral horns of the spinal cord deal with motor impulses.) Between the CNS and the target there are always TWO NEURONS. There is a ganglion (bundle of fibers) that stretches to the target cell. The first neuron is the preganglionic neuron and the second is the postganglionic neuron. The parasympathetic system has 3 types of targets: smooth muscle, cardiac muscle, and glands. There are also two types of receptors on the dendrites of the neurons. 1) nicotinic receptors: which increase the level of activity, cause target to be excited, and 2)muscarinic: cause an inhibatory effect on target. The first neuron from the CNS always releases the excitatory neurotransmitter acetylcholine ACh, therefore the dendrites on the postganglionic must be nicotinic. The action potential from the postganglionic neuron will then determine the effect on the target.
The majority of people today have to get their wisdom teeth (third molars) extracted to avoid their teeth from becoming impacted. If you have had your wisdom teeth taken out you know that your jaw and lips are numb for quite some time following the procedure. I researched the nerves involved in the extraction of wisdom teeth and found that they numb the lingual nerve, which branches off of the mandibular nerve of the trigeminal nerve (cranial nerve V3). This nerve provides sensation for the lower lip, teeth and gums. The maxillary branch (V2) of the Trigeminal (V) nerve provides sensation to the superior lip, teeth, and gums. To quote a site which explained the procedure of numbing nerves, "In regional anesthesia, a numbing medication is injected around the nerves that transmit pain signals from the area involved in the surgery. The procedure “blocks” the nerves, ensuring that you will not feel pain during or immediately after surgery."
Sunday, February 15, 2009
Sunday, February 8, 2009
Wednesday, February 4, 2009 Lecture
During Wednesday's class we focused mainly on the Central Nervous System. We discussed the Meninges (coverings) on the brain, which include 3 distinct layers: the dura, arachnoid, and pia mater. We also learnt about the production of cerebrospinal fluid (CSF) and the flow of CSF throughout the ventricles of the brian and the spinal cord. In addition to CSF, we also discussed the flow of blood to and from the brain, and key facts about the blood flow, such as the anatomical redundancy (that creates a "back-up" flow blood to the brain in case of injury, trauma, etc. The major areas of the brain, the lobes, and their functions were also learnt. Lastly, we discussed seven of the twelve cranial nerves, including the three sensory nerves: I olfactory, II optic, and VIII vestibulocochlear; and four of the motor nerves: III oculomotor, IV trochlear, VI abducens, and XI accessory. We discussed the functions of these 7 cranial nerves, as well as their exit points through the skull.
One disorder that has always been confusing to me is that of blindness. If I were to pick one sense or function to keep over anything else, it would be vision. After our discussion of the optic nerve, one of the twelve cranial nerves, I researched what exactly causes blindness. Although blindness may be caused by such diseases as diabetes or malfunctioning of the retina, one reason it may occur is because of damage to, or the malfuncitoning of, the optic nerve. If the nerve does not develop correctly, blindness may develop from birth, however, one may also become blind if the optic nerve is damaged through trauma.
One disorder that has always been confusing to me is that of blindness. If I were to pick one sense or function to keep over anything else, it would be vision. After our discussion of the optic nerve, one of the twelve cranial nerves, I researched what exactly causes blindness. Although blindness may be caused by such diseases as diabetes or malfunctioning of the retina, one reason it may occur is because of damage to, or the malfuncitoning of, the optic nerve. If the nerve does not develop correctly, blindness may develop from birth, however, one may also become blind if the optic nerve is damaged through trauma.
Sunday, January 25, 2009
Wednesday, January 21, 2009 Lecture
Our lecture consisted primarily of information based on the nervous system, but also dealt with a brief description of embryology, or the study of the development of a fertilized egg. After labeling the various parts of a typical neuron we discussed the significance of myelin. Myelin ultimately speeds up communication along a neuron since messages can "jump" across the myelin sheath (saltatory conduction). In the Central Nervous System, glial called oligodendrocytes myelinate several axons at once. This is why a damaged nerve cannot regenerate in the CNS since oligodendrocytes cover more than one axon, they do not have the ability to regenerate a single axon. The Schwann Cells are responsible for myelinating the cranial and spinal nerves in the Peripheral Nervous System. Each Schwann Cell covers one axon so if a nerve is damaged in the PNS, Schwann Cells have the ability to regenerate that particular nerve, and subsequently one may eventually regain feeling/mobility of the damaged body part.
Although there are 50 to 60 different types of neurotransmitters, one neuron can only produce one neurotransmitter--although it can be stimulated by more than one type of neurotransmitter. The axon hillock is a region where the cell body tapers into the axon and is a critical region where "voltage-regulated ion channels" exist. Voltage-Regulated Ion Channels are protein channels that open or close because of ionic concentration changes. In contrast, Chemical-Regulated Ion Channels, such as those embedded in the dendtritic tree, react to the binding of specific chemicals or neurotransmitters. We went on to discuss how ion channels play a significant role in Action Potentials and how depolarization and repolarization affect the transmission of neurotransmitters. Calcium, as we previously know plays not only a critical role in muscle contraction, but also in moving synaptic vesicles to the synaptic bulbs for the release of the neurotransmitter. Calcium in the extracellular fluid is regulated by astrocytes--a type of ganglion. Our brief overview of embryology covered the primary germ layers in a blastocyst: the endoderm, mesoderm, and ectoderm (which gives rise to the skin and nervous systems). We also covered the primary and secondary brain vesicles that grow within 3 and 6 weeks, respectively.
Primary Brain Vesicles Secondary Brain Vesicles
Prosencephalon---------------->Telencephalon (cerebral hemispheres)
Diencephalon: thalamus, hypothalamus, epithalamus
Mesencephalon----------------->(doesn't further differentiate)
mid-brain, corpora quadrigemina
Rhombencephalon-------------->Metencephalon: cerebellum, pons
Myencephalon: medulla oblongata
The information dealing with the regeneration of nerve cells in the PNS was a fascinating topic for me. I've always wondered why those who suffer from paralysis can never regain full mobility even though there are hundreds of other medical miracles that occur on a daily basis. The difference between the Schwann Cells and Oligodendrocytes, however, was something very interesting and very new to me. I did some casual research on the topic of paralysis. From the information, I gathered that paralysis is most often caused by damage to the spinal cord (which is part of the CNS, and is myelinated by oligodendrocytes, which lack the ability to regenerate). Paralysis is not only caused by trauma, but can also occur in stroke victims. My grandmother, who suffered a stroke about 5 years ago, was lucky to not lose any of her mobility, but interestingly has lost her sense of taste and smell.
Although there are 50 to 60 different types of neurotransmitters, one neuron can only produce one neurotransmitter--although it can be stimulated by more than one type of neurotransmitter. The axon hillock is a region where the cell body tapers into the axon and is a critical region where "voltage-regulated ion channels" exist. Voltage-Regulated Ion Channels are protein channels that open or close because of ionic concentration changes. In contrast, Chemical-Regulated Ion Channels, such as those embedded in the dendtritic tree, react to the binding of specific chemicals or neurotransmitters. We went on to discuss how ion channels play a significant role in Action Potentials and how depolarization and repolarization affect the transmission of neurotransmitters. Calcium, as we previously know plays not only a critical role in muscle contraction, but also in moving synaptic vesicles to the synaptic bulbs for the release of the neurotransmitter. Calcium in the extracellular fluid is regulated by astrocytes--a type of ganglion. Our brief overview of embryology covered the primary germ layers in a blastocyst: the endoderm, mesoderm, and ectoderm (which gives rise to the skin and nervous systems). We also covered the primary and secondary brain vesicles that grow within 3 and 6 weeks, respectively.
Primary Brain Vesicles Secondary Brain Vesicles
Prosencephalon---------------->Telencephalon (cerebral hemispheres)
Diencephalon: thalamus, hypothalamus, epithalamus
Mesencephalon----------------->(doesn't further differentiate)
mid-brain, corpora quadrigemina
Rhombencephalon-------------->Metencephalon: cerebellum, pons
Myencephalon: medulla oblongata
The information dealing with the regeneration of nerve cells in the PNS was a fascinating topic for me. I've always wondered why those who suffer from paralysis can never regain full mobility even though there are hundreds of other medical miracles that occur on a daily basis. The difference between the Schwann Cells and Oligodendrocytes, however, was something very interesting and very new to me. I did some casual research on the topic of paralysis. From the information, I gathered that paralysis is most often caused by damage to the spinal cord (which is part of the CNS, and is myelinated by oligodendrocytes, which lack the ability to regenerate). Paralysis is not only caused by trauma, but can also occur in stroke victims. My grandmother, who suffered a stroke about 5 years ago, was lucky to not lose any of her mobility, but interestingly has lost her sense of taste and smell.
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