Log in
Biology
2
answers
0
watching
72
views

What are the physiological effects associated with thesehormones that are unrelated to their metabolic actions. What arethe major effects of the following hormones on nutrientsandminerals, using + for stimulatory and - for inhibiotryactions.

a. insulin

b. glucagon

c. epinephrine

d. growth hormone

e. cortisol

f. thyroxine

g. parathyroid hormoen

h. calcitonin

Watch
2
answers
0
watching
72
views

For unlimited access to Homework Help, a Homework+ subscription is required.

Unlock all answers

Get 1 free homework help answer.
Already have an account? Log in
Share
Jarrod Robel
Jarrod RobelLv2
28 Sep 2019
Already have an account? Log in
Share

Related textbook solutions

Molecular Cell Biology
8 Edition,
Lodish
ISBN: 9781464183393
Biology: Science for Life with Physiology
6 Edition,
Belk
ISBN: 9780134555430
Biology
2nd Edition, 2013
Openstax
ISBN: 9781947172517
Concepts of Biology
OER Edition,
Openstax
ISBN: 9781938168116
Essentials of Biology
5 Edition,
Mader
ISBN: 9781259660269

Related questions

PLEASE HELP ANSWER ALL PARTS A-E

“Exon 11 of the insulin receptor gene (INSR) is alternatively spliced in a developmentally and tissue-specific manner. Linker scanning mutations in a 5' GA-rich enhancer in intron 10 identified AGGGA sequences that are important for enhancer function. Using RNA-affinity purification and mass spectrometry, we identified hnRNP F and hnRNP A1 binding to these AGGGA sites and also to similar motifs at the 3' end of the intron. The hnRNPs have opposite functional effects with hnRNP F promoting and hnRNP A1 inhibiting exon 11 inclusion, and deletion of the GA-rich elements eliminates both effects. We also observed specific binding of hnRNP A1 to the 5' splice site of intron 11. The SR protein SRSF1 (SF2/ASF) co-purified on the GA-rich enhancer and, interestingly, also competes with hnRNP A1 for binding to the splice site. A point mutation - 3U→C decreases hnRNP A1 binding, increases SRSF1 binding and renders the exon constitutive. Lastly, our data point to a functional interaction between hnRNP F and SRSF1 as a mutant that eliminates SRSF1 binding to exon 11, or a SRSF1 knockdown, which prevents the stimulatory effect of hnRNP F over expression.” PlosOne 6: e27869.

A. What is the function of a SR protein?

B. What is the function of a hnRNP?

C. What is the significance of having two IR isoforms?

D. What is the significance of the G-rich elements in intron 10?

E. How does genetic disruption of the SRSF1 binding site on exon 11 effect INSR splicing?

1. Reflexes associated with Golgitendon organs prevent skeletal muscles from

a. stretching toofar

b. contracting with too muchforce

c. accumulating too much lacticacid

d. exercising toolong

2. Why do plasma glucoseconcentrations start to decline after prolonged enduranceexercise?

a. Glucagon releasedecreases.

b. Insulin releaseincreases.

c. Cortisol releasedecreases.

d. Glycogen stores aredepleted.

3. During a graded aerobic exercise,

a. SBP gradually increases while DBP remains same or slightlydecreases.

b. SBP remains same or slightly decreases while DBP graduallyincreases.

4. Factor(s) affecting blood pressure is(are)

a. HR.

b. SV.

c. Q.

d. TPR.

e. All of above.

5. Where does waterportion of sweat come from?

a. Inside of muscle cells.

b. Urine.

c. Plasma.

6. End-diastolic volume (EDV) -end-systolic volume (ESV) =

a. cardiac output(CO).

b. mean arterial pressure(MAP).

c. stroke volume(SV).

d. ejection fraction(EF).

7. The major factor affecting blood flow is

a. viscosity ofblood.

b. length of vessel.

c. radius of vessel.

d. shear stress ofvessel.

8. Accumulation of metabolicby-products in muscle (H+,CO2, heat) leads to

a. vasoconstriction.

b. vasodilation.

c. sympatheticactivation.

d. reduced muscle bloodflow.


9. During a grated exercise until the point ofventilator threshold (VT) occurring,

a. pulmonary ventilation (VE) increases proportionally to exerciseintensity increase.

b. pulmonary ventilation (VE) increases disproportionally toexercise intensity increase.

10. Immediately stopping a steady-statesubmaximal exercise, VE steeply decreases. This decrease is dueto

a. decrease in PCO2, H+, and the coretemperature (metabolic effect).

b. decrease in neural input from CNS and feedback from activemuscle.

11. During the recovery period after asteady-state submaximal exercise, VE gradually decrease because

a. decrease in PCO2, H+, and the coretemperature (metabolic effect).

b. decrease in neural input from CNS and feedback from activemuscle.

12. Valsalvamaneuver is dangerous because

a. sore abdominal muscles.

b. a drop in blood pressure if Valsalva maneuver iscontinued.

c. a dangerous rise in blood pressure immediately afterstarting Valsalva maneuver.

d. b and c are correct.

e. All of above are correct.

13. The point atwhich pulmonary ventilation (VE) increases disproportionately withoxygen consumption (VO2) during graded exercise iscalled

a. ventilatory threshold (VT).

b. lactate threshold (LT).

c. anaerobic threshold (AT).

14. Which condition duringexercise induces the right shift of hemoglobin's oxygen-binding affinity curve(Bohr effect)?

a. ADP accumulation

b. lower pH

c. mechanical compression ofmuscle capillaries

d. local hypoxia(low O2)

15. How is bloodpressure response during submaximal exercise different between armsand legs?

a. Arms have a higher.

b. Legs have a higher.

c. They are the same

d. They can't be compared

16. Which of thefollowing does not increase the heart'sstroke volume?

a. Enhanced cardiac filling and ejection

b. Neurohormonal influence

c. Training adaptations that expand blood volume

d. Training adaptations that increase resistance to bloodflow

17. Which of the following willdecrease stroke volume (SV)?

a. increased preload

b. increasedcontractility

c. increased Calcium(Ca2+) concentrations

d. increasedafterload

18. For two athletes with sameVO2max, An athlete who has _____ lactate thresholdpredicts better performance.

a. higher

b. lower

c. It doesn

i need question number nine please

Case Study Section 2 – glycolysis
Based on “Monday at the Metabolic Clinic, Adventures in Glycolysis” by Nancy Boury (National Center for Case Study Teaching in Science)

Background:
You have been chosen for a very competitive undergraduate clinical internship at St. Visintainer’s Hospital and Metabolic Clinic working with Dr. Saccharo, an expert in enzyme deficiency disorders related to glycolysis. Before your first day Dr. Saccharo has asked that you review the reactions of glycolysis and the concept of isoenzymes.

Recall that isoenzymes are groups of enzymes that catalyze the same reaction in that they use the same reactants to product the same products. They may have different genes, tissue expression, developmental timing of expression, and affinities for their substrates. As an example, phosphofructokinase-1 has 3 isoenzyme forms: PFK-L is expressed in the liver and the gene is found on chromosome 21; PFK-M is expressed in the muscle and the gene is found on chromosome 12; and PFK-P is expressed in platelets and the gene is found on chromosome 10.

Question 1:
If a person would be deficient in all 3 forms of PFK-1, this person would .
A. Have lower than normal glycogen stores.
B. Have more mitochondrial activity than normal.
C. Be dead.
D. Produce more energy per glucose molecule because glycolysis would be unregulated.

It is now Monday morning and you are ready to start seeing patients with Dr. Saccharo.

Patient 1:
Ann is a teenager and avid golfer who was referred to the clinic after being refused at the blood drive and tiring easily on the high school golf course during practice. Ann is examined and a blood sample was obtained for analysis of a glycolysis related metabolic panel. The results of her panel is below (levels: + = normal, - = decreased; ++= increased):
Blood Metabolic Panel
Blood Glucose +
Glucose-6-phosphate ++
Fructose-6-phosphate ++
Fructose-1,6,bisphosphate ++
Glyceraldehyde-3-phosphate ++
1,3-bisphosphoglycerate ++
Phosphoenolpyruvate ++
Pyruvate -
ATP -
Red Blood Cell Concentration -
Question 2:
Assuming that Dr. Saccharo is correctly assuming that Ann has a defect in glycolysis, what glycolytic enzyme is the most likely to have the defect based on the blood metabolic profile?
A. Hexokinase
B. Phosphofructokinase
C. Triose Phosphate Isomerase
D. Pyruvate Kinase
E. Aldolase

Patient 2:
Marie is a 32-year-old mother of three complaining of fatigue and muscle cramps with exercise. She had always blamed her intolerance to exercise on her sedentary lifestyle. However, she recently joined a gym and after a week of aerobics classes went to her physician, who ordered a series of blood tests. The blood work came back with abnormal results, leading to her muscle biopsy and referral to the metabolic clinic. Marie’s blood was subjected to the same metabolic panel used before with the following results:
Blood Metabolic Panel
Blood Glucose +
Glucose-6-phosphate ++
Fructose-6-phosphate ++
Fructose-1,6,bisphosphate -
Glyceraldehyde-3-phosphate -
1,3-bisphosphoglycerate -
Pyruvate -
ATP -
Red Blood Cell Concentration -

Marie’s muscle biopsy was also analyzed and showed an excess of glycogen.


Question 3:
What is the most likely enzyme deficiency for Marie?
A. Hexokinase
B. Phosphofructokinase
C. Triose Phosphate Isomerase
D. Pyruvate Kinase
E. Aldolase

Question 4:
If you wanted to test the ability of red blood cells to complete glycolysis what compound would you try to detect?
A. Fructose-6-phosphate
B. Aldolase
C. Pyruvate
D. Phosphofructokinase
E. Dihydroxyacetone phosphate


Question 5:
If you used a sample of Marie’s blood for this, what compound could you add to enable these cells to complete glycolysis?
A. Glucose
B. Fructose-1,6-bisphosphate
C. Insulin
D. Glucagon
E. Fructose-6-phosphate


Patient 3:
Leo is a 25-year-old accountant that is not anemic, has perfect teeth, but has experienced two fainting spells recently. One happened after accidentally drinking a non-diet soda; the other after eating “naturally sweetened” fruit salad. His dentist referred him to Dr. Saccharo’s clinic. Dr. Saccharo suspects Leo may have Hereditary Fructose Intolerance (HFI) and has recommended a closely monitored fructose tolerance test.

Hereditary Fructose Intolerance is a recessive disorder where individuals lack a functional copy of one isoform of the enzyme aldolase, specifically Aldolase B (also known as fructose-1-phosphate aldolase). In the liver, fructose is phosphorylated by Fructokinase to fructose-1-phosphate, then is cleaved by Aldolase B to glyceraldehyde and dihydroxyacetone phosphate. Fructose-1-phosphate is also a known allosteric inhibitor of Glycogen Phosphorylase, the primary enzyme responsible for releasing glucose from glycogen.

Question 6:
As compared to a normal individual that consumes fructose, a person with HFI who ingested fructose would have (select all that apply):
A. High levels of blood fructose
B. High levels of blood fructose-1-phosphate
C. High levels of blood glucose
D. Low levels of blood fructose
E. Low levels of blood glucose


That afternoon Leo undergoes the fructose tolerance test with the following results:

Question 7:
Based on the results of the test, what was the effect of giving Leo the intravenous fructose?
A. A rise in blood glucose levels
B. A decrease in blood glucose levels
C. An increase in glycogen stores
D. A rapid drop in blood pressure


However there were complications: Soon after the test Leo orders and drinks a cup of tea, but after half the cup Leo passes out. Dr. Saccharo orders two sequential blood glucose checks. The first was 50 mg/dl and 15 minutes later Leo’s blood glucose was down to 40 mg/dl. With those results Dr. Saccharo injected something into Leo’s IV and within minutes Leo was back to normal.

Question 8:
From these results does it appear that Leo has HFI?
A. Yes
B. No
C. It is unclear from the results


Question 9:
What did Dr. Saccharo inject into Leo’s IV line?
A. Insulin
B. Glucagon
C. Glucose
D. Fructose
E. Phosphofructokinase

Dr. Saccharo puts Leo on a restricted diet and orders follow-up visits.

Question 10:
Which of the following foods/ingredients would Leo NOT be allowed to eat?
A. Artificial sweeteners
B. High starch foods, such as potatoes
C. Sweet tea made with cane sugar
D. Any dairy products

Dr. Saccharo puts Leo on a restricted diet and orders follow-up visits.

Case Study Section 2 – glycolysis
Based on “Monday at the Metabolic Clinic, Adventures in Glycolysis” by Nancy Boury (National Center for Case Study Teaching in Science)

Background:
You have been chosen for a very competitive undergraduate clinical internship at St. Visintainer’s Hospital and Metabolic Clinic working with Dr. Saccharo, an expert in enzyme deficiency disorders related to glycolysis. Before your first day Dr. Saccharo has asked that you review the reactions of glycolysis and the concept of isoenzymes.

Recall that isoenzymes are groups of enzymes that catalyze the same reaction in that they use the same reactants to product the same products. They may have different genes, tissue expression, developmental timing of expression, and affinities for their substrates. As an example, phosphofructokinase-1 has 3 isoenzyme forms: PFK-L is expressed in the liver and the gene is found on chromosome 21; PFK-M is expressed in the muscle and the gene is found on chromosome 12; and PFK-P is expressed in platelets and the gene is found on chromosome 10.

Question 9:
What did Dr. Saccharo inject into Leo’s IV line?
A. Insulin
B. Glucagon
C. Glucose
D. Fructose
E. Phosphofructokinase

Weekly leaderboard

Home
Homework Help 3,900,000
Biology 460,000
Start filling in the gaps now
Log in