BR Bio Set 1 Flashcards

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1
Q

types of glands

A

allows for secretion of substances into luminal space
Exocrine: secretion via duct
Endocrine: secretion via blood

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2
Q

neuromuscular junction pathway

A

As the action potential reaches the end of the axon, it triggers opening of calcium channels, causing synaptic vesicles to fuse w the pre-synaptic membrane for release of ACh into the synaptic cleft.

The released neurotransmitters diffuse through the synaptic cleft and bind to the post-synaptic membrane receptors, inducing conformational change of those receptors into a ligand-activated channel (ionophore) that is large enough to allow cations (such as Na+) to pass through

As cations enter the post-synaptic membrane, the muscle fibers depolarize and another action potential in the receiving neuron is eventually generated, thus allowing for propagation of the nerve signal

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3
Q

recycling in the neuromuscular junction

A

Calcium is recycled via endocytosis.

ACh, if left in the cleft, would continue to bind and allow cation diffusion, thus causing prolonged muscle spasms.

    • To prevent this, an enzyme acetylcholinesterase (bound to the surface of the postsynaptic membrane) hydrolyzes acetylcholine into acetate and choline.
    • These products are then recycled when they are transported back into the pre synaptic terminal, where they are used in the synthesis of acetylcholine.
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4
Q

excitatory v inhibitory postsynaptic potentials

E/IPSP

A

Whereas EPSP lead to an increase of the permeability of the postsynaptic membrane to positively charged ions, thus making depolarization more likely

vs. IPSP … negatively charged ions, thus making hyper-polarization more likely

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5
Q

cerebral cortex

  • types of matter
  • landmarks
A

Cerebral cortex: outermost layer of cerebrum
– Grey matter: nerve cell bodies and their dendrites
– White matter: myelinated axons of the nerve cells
Note: the matters are reversed in the case of the spinal cord

Landmarks of the cerebral cortex

    • Central sulcus: prominent groove that separates the front lobes and parietal lobes
    • Motor cortex: anterior to the sulcus; controls movement of individual muscles
    • Sensory cortex: posterior to sulcus; detects sensations in various parts of the body via somatic receptors in the PNS
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6
Q

mono/polysynaptic reflex arc

eg. hammer impinging on the patellar tendon

A

As the hammer impinges on the patellar tendon, sensory neurons in the tendon become excited, sending impulses that travel along an axon to enter the spinal cord. They enter through the dorsal root ganglion and synapses with two neurons.

Monosynaptic reflex arc: One synapse is made to a motor neuron that immediately leaves the spinal cord and returns to the quadricep muscle, causing a contraction
– The quadriceps muscle is termed an extensor muscle because it extends (or straightens) the leg at the knee joint

Polysynaptic reflex arc: the other synapse is made to an interneuron that will, in turn, synapse with a different motor neuron that innervates the “hamstring” (bicep) in the back of the leg.
– The hamstring is termed a flexor muscle bc it bends (or flexes) at the knee joint

*** The contraction of one muscle inhibits the contraction of the other, THUS, in the patellar tendon example, only the monosynaptic reflex arc is followed through while the polysynaptic one is inhibited. This is observed as a smooth and coordinated movement at the knee joint where the lower portion o f the leg extends outwards.

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7
Q

What are the differences btwn the somatic and autonomic nervous system?

A

Somatic:

    • Once nerve fibers leave CNS, they do not make a synapse until they have reached their effector organ
    • At this organ, the neurotransmitter that is released is ACh
    • Specifically, the CNS innervates the skeletal muscle

Autonomic:

    • Once the nerve fibers leave the CNS, they synapse with a ganglion before making their final synapse with their effector organ
  • —– Exception: adrenal medulla
    • Only the preganglionic fibers release ACh; post will release norepinephrine
    • Specifically, the ANS innervates glands, smooth muscle, and cardiac muscle
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8
Q

what is overlap in tactile discrimination and how does it affect our perception of the environment

A

Recall that the end of a neuron can be divided into many branches, which can in turn end at a receptor → these constitute a receptive field

    • Depending on which area of the body, receptive fields are plentiful and can overlap – or there are very few, with no overlap
    • Overlap means that we are stimulating more than one receptive field – which means we might feel that more than one area of the body is being stimulated when, really, it’s only a part of more than one receptive field.

LATERAL INHIBITION, mediated through interneurons within the spinal cord

    • The axon that leads away from the field has lateral connections to interneurons that inhibit the impulses being sent down the axons from the other receptive fields
    • Thus, only the appropriate signal will be sent to the brain for inference, rather than multiple
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9
Q

order of sensory neurons

A

There are FIRST-ORDER neurons carrying information from the receptive field(s) that enter the spinal cord and synapse with SECOND-ORDER neurons that ascent on the opposite side of the spinal cord to the thalamus. Then, another synapse is made with THIRD-ORDER neurons that continue to ascent until they reach a specific region of the somatosensory cortex for interpretation

The cerebral cortex itself contains cells that are organized into six horizontal layers

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10
Q

arteries

A

AWAY FROM THE HEART

durable because of the high pressure that comes with moving blood from the heart through the rest of the body → thus they have thick walls composed of both smooth muscle and connective tissue that contain both collagenous and elastic fibers

Elasticity prevents the blood pressure from becoming too high when it is ejected out of the heart but also maintains the high arterial pressure btwn the high systolic and diastolic phases of the heart → thus, allows blood flow to the rest of the circulatory system without sudden loss of pressure

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11
Q

capillaries

A

GAS EXCHANGE

Walls are composed of a unicellular layer of endothelial cells, surrounded by a basement membrane → thin layer allows for diffusion
Note: unlike the arteries, there is no connective tissue or smooth muscle

Capillary itself is just barely large enough for a red blood cell to squeeze through

Precapillary sphincter: regulates entry to the capillary bed; made of smooth muscle

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12
Q

veins

A

TOWARDS THE HEART

Due to the lowered BP in veins, the amount of smooth muscle and elastic tissue surrounding the veins is reduced → instead, veins use sympathetic nerves to control specialized valves

Specialized valves ensure blood flow happens in only one direction and prevent backward flow
– These valves can become damaged, thus allowing backward flow, thus increasing the pressure in veins → this damage is observed by the human eye as varicose veins, which are protrusions of the dilated veins beneath the skin

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13
Q

blood clotting

- factor X > II > XIII > vitK and Ca2+

A

the intrinsic and extrinsic pathways converge at factor X. Intrinsic factors are produced in the vessels, extrinsic factors are produced by the liver.

Factor Xa (the a just means activated) activates Factor II. Factor II is also called thrombin

Factor IIa converts fibrinogen to fibrin. Fibrin forms a weak clot by binding to a mass of platelets. Those platelets became stuck to each other because of thromboxane, ADP and serotonin that were produced upon vessel injury. So first develops a mass of platelets stuck to each other loosely. Then comes fibrin and forms a string around them–making a stronger, but still relatively weak clot.

Factor IIa also activates Factor XIII, which is a transglutaminase. Factor XIIIa links individual fibrin molecules together, making a strong clot.

Vitamin K is required to add an additional carboxylic acid to a glutamate residue on thrombin (and a few other factors). This makes that glutamate on thrombin have a negative 2 charge and allows it to bind Calcium ions.

The calcium ions complexed with thrombin are what allow the thrombin to stay near the plasma membrane. The plasma membrane is negatively charged, and the calcium is attracted to the membrane. This allows the clot to develop at the site where the vessel is broken. The breaks always occur on the edges of the vessels, so right where the epithelial plasma membranes are.

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14
Q

How does fat diffuse?

A

Fats are degraded into fatty acids and glycerol by lipases for diffusion into the intestinal epithelial cells

Once across the membrane, they resynthesize back into fats / triglycerides and aggregate into structures called chylomicrons

These aggregates or chylomicrons are released at the basolateral membrane and into the extracellular space, where they enter the lymph and are transported to the veins and eventually the tissues

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15
Q

kidneys

  • nephron
  • glomerulus
  • bowman’s capsule
  • blood plasma
  • tubular structure
A

Functional unit of the kidney is the NEPHRON, consisting of the glomerulus (aka “little ball”), Bowman’s capsule, and a tubular system

Glomerulus: collection of capillaries that receive blood from an artery terminating in the renal system; hydrostatic pressure from the heart forces the blood to enter the Bowman’s capsule

Bowman’s capsule: contains a cell-free ultrafiltrate that lacks many of the plasma proteins found in the blood → basically, plasma minus the (large molecular weight) proteins

Blood plasma: 90% water + organic (ie proteins, sugars, amino acids, etc) + inorganic (ions) materials + red / white blood cells + platelets

Extending from BC is a long tubular structure which is divided into the proximal convoluted tubule (PCT), loop of Henle, distal convoluted tubule (DCT) and the collecting duct

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16
Q

tubular structure of the nephron

  • osmolarity
  • PCT
  • loop of henle
  • DCT
  • collecting duct
A

Osmolarity of filtrate in BC and PCT is about 300 milliosmols per liter, which is about the same for plasma.

PCT: obligatory section of nephron bc roughly 65% of all reabsorption / secretion occurs here; basically reabsorbs glucose, small molecular weight proteins, amino acids, and vitamins + most of Na+, Cl-, and water;

As the PCT begins to descent from the cortex into the medulla, it forms the loop of Henle, which has a descending thin and an ascending thin then thick portion

    • Descending thin: more permeable to water than other ions and molecules
    • Ascending thin: more permeable to other ions and molecules than water
    • Ascending thick: more permeable to other ions than water and molecules
  • —- THUS: as the filtrate is passing up, the osmolarity decreases, thus increasing the concentration of water → results in a more dilute fluid

DCT split into two parts as well

  • close to LoH is also quite impermeable to urea and water but still rather permeable to ions like sodium → thus, more dilution
  • but the segment closer to the collecting duct / cortical region of kidney are still impermeable to urea but permeable increases to other ions beyond sodium

Collecting duct is the area of action for aldosterone and the antidiuretic hormone.
- urine collected will be emptied into the ureter, which transports urine to the bladder for storage until the body exits the body via the urethra

17
Q

GnRH

A

Gonadotropin releasing hormone (GnRH) is released from the hypothalamus, signalling the anterior pituitary to release the gonadotropins luteinizing hormone (LH) and follicle stimulating hormone (FSH)

Both LH and FSH travel down to the gonads

    • Male gonads are the testes
    • Female gonads are the ovaries

The response that these gonadotropins elicit can be divided into two general responses

    • Production of steroid hormones; eg. Estrogen in females and Testosterone in males
    • Production of germ cells; Male germ cells are called spermatozoa, and Female germ cells are called ova
18
Q

Pathway of sperm

A

Testes: location of spermatogenesis (formation of sperm)

Epididymis: storage for mature sperm

Vas deferens: transports sperm from the epididymis to ejaculator ducts via contraction of smooth muscle

Ejaculatory ducts: transports sperm from vas deferens to the erthra, but allows the addition of various components by the following → final product after these additions is semen

    • Seminal vesicles
    • Prostate
    • Bulbourethral glands

Penis (urethra)

19
Q

Spermatogenesis

  • definition
  • structures / cells involved
A

development of sperm; requires a lower temperature than that of the body, which is why it happens in the testes (which sit in the scrotum outside the body cavity)

Within each testis are a series of convoluted tubules called the seminiferous tubules
Within these tubules are the spermatogenic cells

Leydig cells: specialized interstitial cells that lie outside the seminiferous tubules; produces the hormone testosterone
vs. Sertoli cells: regulate spermatogenesis by selectively producing the protein hormone inhibin

20
Q

Spermatogenesis

- cross section

A

Luminal space in the center contained by a ring of Sertoli cells, which are in contact with the basement membrane and spermatogenic cells

The basement membrane separates the Sertoli cells from the interstitial / Leydig cells

As you proceed from the basement membrane of the tubules toward the lumen, the cells become more and more differentiated / developed
– Different developmental events take place on different sides of the Sertoli cells, specifically in the way that spermatogenic cells divide.

21
Q

Spermatogenesis

  • pathway
  • naming
A

The spermatogenic cells that are closer to the basement membrane are called SPERMATOGONIA, or PRIMARY SPERMOCYTES —- They have 46 chromosomes and will divide by mitosis, thus the resulting “daughter cells” are exactly the same as the parental cell and undergo constant division

As the primary spermatocytes form, they begin to squeeze by the juxtaposed Sertoli cells and move towards the lumen of the seminiferous tubules

Primary spermatocytes near the lumen undergo meiosis that will reduce their genetic complement to 23 chromosomes. After the first meiotic division, they are now called SECONDARY SPERMATOCYTES.

A second meiotic division takes place, thus yielding two daughter cells that are called SPERMATIDS; they have half the chromosomal complement as the original spermatogonia.
– Every primary spermatocyte that undergoes mitosis and meiosis ends up producing FOUR spermatids, which are all connected to each other by cytoplasmic bridges

Spermatids are then transformed into a SPERMATOZOA by “budding” out of the original spermatid form. → kind of like a butterfly emerging from a chrysalis

22
Q

structures of the spermatozoa

A

fully developed sperm

Acrosome: located at the tip; contains digestive enzymes that help the spermatozoa gain access to the interior of the egg once fertilization has taken place

Head: contains the nucleus (thus contains DNA)

Midsection: contains mitochondria, which provide energy for the whipping movement of the tail

Tail: enables the sperm to swim towards the egg

23
Q

hormonal control of sperm production

A

Recall that Leydig cells can produce testosterone (aka T) by converting cholesterol; this hormone can diffuse out of the cell and target different tissues, each with a different effect.
– In Sertoli cells, T binds to a specific receptor and is converted to a compound called dihydroT (aka dHT); this complex then diffuses into the nucleus of the Sertoli cell and instruct the DNA to synthesize RNA. It is the products of such RNA synthesis that affect spermatogenic cells (recall that Sertoli cells are in direct contact with spermatogenic cells).

Recall that the hypothalamus release GnRH, which causes the release of FSH and LH, which act on the gonads. Both FSH and LH have effects on Leydig cells and Sertoli cells.

    • LH binds to a specific receptor on the membrane on Leydig cells, producing a second messenger that increases the conversion of cholesterol into T.
    • FSH binds to a specific receptor on the membrane of Sertoli cells, inducing a secondary response that promotes the conversion of T into dHT and also the synthesis of receptors.
  • —- Male contraceptives focus on preventing the production of FSH or dHT.
24
Q

feedback mechs w sperm production

A

POSITIVE FEEDBACK
High levels of dHT trigger the production of inhibin by Sertoli cells.

NEGATIVE FEEDBACK
T, generated by Leydig cells, inhibits the synthesis of GnRH and LH.

Inhibin, generated by Sertoli cells, negatively modulates the anterior pituitary, thus affecting LH and FSH production.
Eg. if dHT levels are too high, there is an increase in inhibin levels, which decreases the overall levels of FSH

Gonadotropin levels are relatively constant bc of the constant synthesis of spermatogenic cells.

25
Q

pathway of egg

A

Ovaries: site of semi-maturation

Fallopian tubes: aka oviduct; site of fertilization

Uterus: site of implantation by the blastocyst

Vagina: exit channel

26
Q

oogenesis

  • definition
  • pathway
  • naming
A

production of female germ cells

OOGENIA will divide via mitosis to form PRIMARY OOCYTES, which have 46 chromosomes

With the surge of LH, primary oocytes will undergo their first meiotic division, forming the SECONDARY OOCYTES w 23 chromosomes. This occurs in monthly cycles.
– During this division one of the two daughter cells will obtain ALL the cytoplasm while the other cell is just a small sphere of DNA; this smaller sphere is referred to as the first POLAR BODY.

The secondary oocyte begins meiosis but is then arrested in Metaphase II to await fertilization

    • ONLY AFTER fertilization has taken place, thus generated the OVUM and a second polar body.
    • Thus, for one viable ovum, there are three other nonviable polar bodies.

When sperm and ovum unite in fertilization, the complement of 46 chromosomes will be restored (23 from the male and 23 from the female).

27
Q

menstrual stages

A

1: Follicular phase. This begins with the “end” of menstruation (the bleeding). Follicles will develop until only one is selected to form the zona pellucida, which is then surrounded by more follicle / granulosa cells, then finally the theca cells. Estradiol is increasing. Here, all of the hormones are participating in a kind of negative feedback, so LH and FSH are being kind of inhibited but slowly grow until…
2: Ovulation. surge of hormone LH will surge triggers the first meiotic division and the beginning of the second, but also causes follicle to rupture and spit out the secondary oocyte, which is arrested in metaphase II
3: Luteal Phase. The ruptured follicle becomes the corpus luteum, which produces estrogen and progesterone. Estrogen establishes the endometrium and progesterone kind of keeps it up. Here, the progesterone and estrogen levels are high (although estrogen will begin to drop and it is not as high as it was during estrogen!)
4: Menstruation again. Eventually, if there is no fertilization, the corpus luteum will degrade, causing estrogen and progesterone levels to drop enough that the endometrium cannot be kept up and it will shed. This is the bleeding and whatnot.

28
Q

After fertilization, what happens

  • 7 days
  • first 3 months
  • last 6 months
A

basically what happens after sperm and ovum fuse to form a zygote w a complete set of 46 chromosomes

In about 7 days, the zygote will attach itself to the uterine lining

When implantation takes place, the placenta (made of maternal and fetal cell types) begins to form; the placenta synthesizes chorionic gonadotropin (CG) which stimulates the corpus luteum to continue making estrogen and progesterone instead of degrading.
– Estrogen and progesterone generated by the corpus luteum at this stage have the added effect of promoting the growth of mammary glands; the anterior pituitary, although inhibited by est/progest in making LH and FSH, will instead generate prolactin, which also promotes the growth of mammary glands.

During the last six months of pregnancy, CG is no longer made, resulting in the degradation of the corpus luteum, meaning the est/progest production is also stopped. At this point in time, the placenta is able to begin synthesizing est/progest on its own.

29
Q

what do pregnancy tests measure

A

Pregnancy tests detect chorionic gonadotropin in the bloodstream (made by the placenta to maintain the corpus luteum), as CG is only made during the first three months of pregnancy

30
Q

fate of the three germ layers

A

Ectoderm: skin, lens of eye, brain, nervous system

Mesoderm: notochord, heart, skeleton, muscle, outer coverings of internal organs, reproductive organs

Endoderm: inner lining of digestive tract and respiratory tract, major glands of the body

31
Q

neurulation

  • notochord
  • neural crest
A

Germ layers begin to form the structures that will eventually define the embryo (at this point called the neurula) and, later, the adult

Formation of NOTOCHORD takes place along body midline from the mesoderm.

    • Superior to notochord is the neural plate, which is a mass of ectodermal cells. These will fold in on themselves to form the neural groove, with the edges fusing together to form the neural tube. → Within this tube, the spinal cord will form anterior to the brain; thus the neural plate gives rise to the nervous system
    • This tissue is referred to as primordium as it is the earliest stage of development of a structure.

Formation of the NEURAL CREST, Refers to the set of specificalized cells (neural crest) left in the more dorsal position of the neural tube that begin to move to the sides of the developing embryo and they begin to functionalize, thus forming the sensory cells and the adrenal medulla

32
Q

Organogenesis

A

ORGANOGENESIS relies on interactions btwn the ectoderm and mesoderm

The neural tube elongates and thins out, forming the anterior to posterior developmental gradient
– As the neural tube continues to form segments of mesodermal tissue, somites begin to appear; these will eventually give rise to the vertebrae, connective tissue, and muscles of the body.

Neural crest cells begin to migrate and take up positions in the vicinity of the neural tube.

    • Mesodermal cells migrate toward the neural tube, eventually forming the vertebral column.
    • The brain begins to form at the anterior portion of the neural tube, as well as optic vesicles
33
Q

oxytocin

A

responsible for contractions during birth, as well as during breastfeeding

34
Q

Define the following:

  • theca cells
  • granulosa cells
  • leydig cells
  • sertoli cells
A

Theca cells: analogous to the Leydig cells in the male; convert cholesterol into testosterone in the presence of LH
Granulosa cells: analogous to the Sertoli cells in the male; nourish developing oocyte, produce inhibin, steroids and LH receptors in presence of FSH

Leydig cells: analogous to the Theca cells in the female; convert cholesterol into testosterone in the presence of LH
Sertoli cells: analogous to the Granulosa cells in the female; nourish sperm, produce inhibin, and secrete androgen-binding protein in presence of FSH