The chapters numbers on this site which relate to what we have studied are:
5, 6, 7, 8, 9 and parts of 25 and 27.
And for something to smile about... Don't be this person, study!
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“Education, therefore, is a process of living and not a preparation for future living.” ~ John Dewey
Mr. Zuma's pledge marks a departure from the policies of his predecessor, President Thabo Mbeki, who disputed the scientific evidence linking HIV with AIDS, and who actively discouraged the rollout of antiretroviral treatments to help AIDS patients live longer, more productive lives.
Speaking to an enthusiastic crowd in the nation's capital in Tshwane (Pretoria), Zuma compared the fight against AIDS with the struggle for freedom against the white-racist rule of apartheid.
"That time has now come in our struggle to overcome AIDS," Zuma said. "Let us declare now, as we declared then, that we shall not submit." To read the full article, click here.
In an amazing co-incidence, we managed to start our short unit on HIV on World AIDS Day.
Today we focused on the structure of HIV as well as its life cycle. Click here to see the video we watched in class on the life cycle of HIV.
Using red paper, make muscles for the quadriceps, hamstrings, biceps and triceps. Label these muscles, as well as write a brief description of how muscles work.
Drug addiction is a complex brain disease. Preventing drug abuse and addiction and treating the disease effectively require understanding the biological, genetic, social, psychological, and environmental factors that predispose individuals to drug addiction.
Individuals make choices to begin using drugs. Some people begin using drugs to relieve a medical condition and then continue to use the drugs after the medical need is over. Children who are depressed or who have a psychiatric disorder sometimes begin using illicit drugs to self-medicate. Other people begin taking drugs to feel pleasure, to escape the pressures of life, or to alter their view of reality. This voluntary initiation into the world of addictive drugs has strongly influenced society's view of drug abuse and drug addiction and their treatment.
When does drug abuse become drug addiction? No one becomes addicted with the first use of a drug. Drug abuse and drug addiction can be thought of as points along a continuum. Any use of a mind-altering drug or the inappropriate use of medication (either prescription or over-the-counter drugs) is drug abuse, but the point when drug abuse becomes drug addiction is less clear. Different drug abusers may reach the point of addiction at different stages. Scientists continue to investigate the factors that cause the switch between the two points.
Figure 4.1: The continuum of drug abuse and addiction. |
Currently, drug addiction is defined as the continued compulsive use of drugs in spite of adverse health or social consequences.1 Drug addicts have lost control of their drug use. Individuals who are addicted to drugs often become isolated from family or friends, have difficulty at work or school, and become involved with crime and the criminal justice system. For addicts, continuing their drug habit becomes their primary focus in life.
Certain drugs, including opiates and alcohol, cause strong physical reactions in the body when drug use stops. When a heroin addict stops taking heroin, he or she can experience a variety of symptoms ranging from watery eyes and a runny nose to irritability and loss of appetite and then diarrhea, shivering, sweating, abdominal cramps, increased sensitivity to pain, and sleep problems.2 In general, withdrawal from heroin makes the abuser feel miserable. Withdrawal from other drugs, such as cocaine and amphetamines, does not lead to strong physical reactions. For most drugs, physical withdrawal symptoms can usually be controlled effectively with medications. Even though withdrawal from some drugs does not cause the abuser to have physical reactions, stopping drug use is difficult because of the changes the drugs have caused in the brain. Once the drugs stop, the abuser will have cravings, or intense desire for the drugs.3 Craving arises from the brain's need to maintain a state of homeostasis that now includes the presence of the drug. A person may experience cravings at any stage of drug abuse or addiction, even early in the experimentation phase of drug abuse. Cravings have a physical basis in the brain. Using PET imaging, scientists have shown that just seeing images of drug paraphernalia can stimulate the amygdala (part of the brain that controls memory) in drug addicts.4
Drugs of addiction do not merely cause short-term changes in an individual's cognitive skill and behavior. A drug "high" lasts a short time, ranging from less than an hour to 12 hours, depending on the drug and dose. The changes in the brain that result from continued drug use, however, can last a long time. Scientists believe that some of these changes disappear when drug use stops; some disappear within a short time after drug use stops, and other changes are potentially permanent. One of the first changes in the brain that occurs in response to repeated drug abuse is tolerance. Tolerance develops when a person needs increasing doses of a drug to achieve the same "high" or "rush" that previously resulted from a lower dose of the drug. Two primary mechanisms underlie the development of tolerance.3 First, the body may become more efficient at metabolizing the drug, thereby reducing the amount that enters the bloodstream. Second, the cells of the body and brain may become more resistant to the effect of the drug. For example, after continued cocaine use, neurons decrease the number of dopamine receptors, which results in decreasing cocaine's stimulatory effect. Opiates, on the other hand, do not cause a change in the number of receptors. Instead the opiate receptors become less efficient in activating the second messenger system, thus reducing the effects of the opiates.
Drugs can cause other long-term changes in the anatomy and physiology of the brain's neurons. Alcohol, methamphetamine, and MDMA (Ecstasy) can kill neurons.3 Unlike other types of cells in the body, neurons in many parts of the brain have little or no capability to regenerate. (Recent studies have shown that the adult human brain can generate new neurons in the hippocampus, a part of the brain important for learning and memory.5 Other parts of the brain do not show this ability.) Alcohol kills neurons in the part of the brain that helps create new memories. If those neurons die, the capability for learning decreases. Methamphetamine kills dopamine-containing neurons in animals and possibly in humans as well.6 MDMA kills neurons that produce another neurotransmitter called serotonin.7 In addition to neurotoxic effects, drugs can significantly alter the activity of the brain. PET scans of cocaine addicts show that the metabolism of glucose, the primary fuel for cells, is drastically reduced in the brain, and that this decrease in metabolism can last for many months following cessation of drug abuse.8
In addition to the functional and anatomical changes in the brain, drug abuse puts addicts at higher risk for other health problems. For example, inhalant abuse can lead to disruption of heart rhythms, and snorting cocaine can lead to ulcerations in the mucous membranes of the nose. In addition, drug addicts are at increased risk of contracting HIV or AIDS through shared needles. Similarly, hepatitis B and hepatitis C are much more common among drug addicts than the general population. Tuberculosis is another concern. Drug abuse and addiction also are contributing factors in motor vehicle accidents.
Animals as Research Models
Why do scientists study the brains of nonhuman animals? Scientists use animals in research studies because the use of humans is either impossible or unethical. For example, when scientists investigate the effects of drugs of abuse on brain function, either the question they are asking cannot be answered in a living human or it would be inappropriate to give drugs to them.
The use of animals as subjects in scientific research has contributed to many important advances in scientific and medical knowledge. Scientists must analyze the goals of their experiments in order to select an animal species that is appropriate. Scientists often use fruit flies (Drosophila melanogaster) when they want to learn more about genetics. However, fruit flies are not a very good model if a scientist is investigating muscle physiology; a mouse may be a better model for those experiments. Although scientists strive to develop nonanimal models for research, these models often do not duplicate the complex animal or human body. Continued progress toward a more complete understanding of human and animal health depends on the use of living animals.
Scientists who use animals as research subjects must abide by federal policies that govern the use and care of vertebrate animals in research. The Public Health Service established a policy that dictates specific requirements for animal care and use in research. This policy conforms to the Health Research Extension Act of 1985 (Public Law 99-158) and applies to all research, research training, biological testing, and other activities that involve animals.14 The principles for using and caring for vertebrate animals in research and testing are as follows:
G Block: yours is due on Wednesday Nov. 11
D & F blocks: yours is due on Thursday Nov. 12
Go to: www.cancer.org
Under “learn about cancer” click choose a topic. No students in the same class may have the same topic.
Here are the guidelines:
1 page
2-3 figures/pictures
Name of your type of cancer:
Causes/treatments
Signs/symptoms
Diagnosis
Stages
2-3 key stats
A footer or use footnotes to cite your sources. Print the flyer on the colored sheet of paper you were given in class. You most certainly may embellish your flyer with markers/crayons/colored pencils. You will share this with the class the day it is due.
NOTE: The majority of students in F and G blocks did not remember to bring their computer to class, so they picked their cancer topics and spent the remainder of class reading and answering questions from the "What is Cancer?" packet. If you are in F or G block, please make sure you bring your computer to class on Tuesday.
Please answer the questions below honestly. I appreciate your thoughts and am doing this so that I can be a better teacher.
2. Do not write on this sheet of paper.
3. TYPE your answers, using Times New Roman Font, size 12, with 1.5 spacing.
1. What is the chemical structure and function of ATP? (5 points)
2. Draw and label a chloroplast, include all structures and say where each phase of photosynthesis takes place. (10 points)
3. What are the two phases for photosynthesis? (2 points)
4. Describe the light dependent reactions in detail. Begin with a photon of light hitting a chlorophyll molecule and finish with the creation of ATP by ATP synthase. (20 points)
5. Draw and label a mitochondria, include all structures and say where each phase of cellular respiration takes place. (10 points).
6. What are the products and reactants of glycolysis?
7. What are the products and reactants of the citric acid cycle?
This is due at the beginning of class on Monday October 26th. Late assignments will not be accepted.
Working with a partner (or in a group of three), you will complete the following two tasks which will be due on Tuesday October 20th. This mini project will count as THREE homework assignments….So….Here is your chance to boost your grade.
Task 2: Write a script for a tour guide leading trips to the light dependent reactions and the Calvin Cycle. Your script should include the following information
Investigating the Effects of pH and Temperature on Enzyme Activity
Background: In this lab exercise we’ll investigate some of the properties of enzymes. Almost all chemical reactions that occur in living things are catalyzed by enzymes. Enzymes are large protein molecules (macromolecules) that catalyze or speed up chemical reactions without being altered themselves. Proteins can be just about any size or shape, which is useful since it’s the shape of an enzyme that determines the reactions it can catalyze. However, enzymes are sensitive to changes in temperature and pH, which alter their shapes and can even destroy catalytic ability (denaturing). Enzymes have evolved to work most efficiently at the temperature and pH found in the part of the organism where they are needed. Many enzymes in the human body function most efficiently at 37oC and at a pH of 7.4.
The enzyme you will investigate is called catalase. Catalase is found in tissues of many organisms (both plants and animals) because it plays a very important role in protecting cells. Its purpose is to destroy toxic substances which may be introduced into cells. Also, some cells use catalase to destroy cellular debris or worn out organelles. Hydrogen peroxide is a normal by-product of cellular metabolism but, it is also toxic to cells. Under normal conditions organisms produce the enzyme catalase that quickly changes hydrogen peroxide into two harmless substances, oxygen and water. However, the function of the enzyme is affected by changes in the environment. Catalase works to break down hydrogen peroxide by the following chemical reaction:
2 H2O2 ------------------>2 H2O+ O2
(Catalase)
Purpose: What is the effect of altering the pH on the function of catalase?
Pre Lab Questions (ANSWER IN COMPLETE SENTENCES IN YOUR LAB NOTEBOOK. This answers should be directly below the procedure that you worked on in class).
1. What is catalase and where is it found in living organisms?
2. What reaction does catalase speed up (catalyze)?
3. Write the correct chemical reaction for hydrogen peroxide being catalysed into water and oxygen.
4. What is the substrate in the chemical reaction?
5. What are the products in the chemical reaction when catalase breaks down hydrogen peroxide?
6. Write hypotheses for how you think changes in pH AND temperature will affect the action of the catalase enzyme in the potato.
Hypothesis for change in pH.
Hypothesis for change in temperature:
Materials:
Safety: HCl and NaOH are strong acids and bases. If you spill these chemicals on your skin, immediately wash in running water. Wear safety glasses at all times. Be careful of hot water and hot plates.
Part A:
1. Label 3 large test tubes hot, cold and room temp.
2. Cut 3 1.5cm3 pieces of potato with peel removed.
3. Use a mortar and pestle to macerate (mash/grind up) each cube.
4. Place ALL of the macerated potato cubes into each labeled test tube.
5. Add 1ml of distilled water to each test tube containing potato mash.
6. Place the test tube labeled hot in the hot water (100oC) bath for 3 minutes.
7. Place the test tube labeled cold in the cold water bath (0-4oC) for 3 minutes.
8. Leave the test tube labeled room temperature in the test tube rack.
9. After 3 minutes, remove the test tube from the baths and allow the hot test tube to cool.
10. Add 5ml of H2O2 (3.0% hydrogen peroxide) to each tube.
11. Wait one minute while reaction occurs then measure the height of the bubbles in each tube in cm.
12. Record in Table 1. Measure the radius of the test tube and record in Table 1.
Part B:
1. Label 3 test tubes acid, base and water.
2. Cut 3 1.5cm3 pieces of potato with peel removed.
3. Use a mortar and pestle to macerate (mash/grind up) each cube.
4. Place ALL of the macerated potato cubes into each labeled test tube.
5. Add 1ml of 0.1M HCl (hydrochloric acid) to the tube labeled acid. Gently mix contents with wooden or glass rods. SEE SAFETY NOTE ABOVE.
6. Test the pH of the solution by dropping a small amount of liquid onto a pH strip. Record in Data Table 2.
7. Add 1ml of 0.1M NaOH (sodium hydroxide) to the tube labeled base. Gently mix contents with wooden or glass rod. SEE SAFETY NOTE ABOVE.
8. Test the pH of the solution by dropping a small amount of liquid onto a pH strip. Record in Data Table 2.
9. Add 1ml of water to the tube labeled water. Mix contents by gently swirling. Test the pH of the solution by dropping a small amount of liquid onto a pH strip. Record in Data Table 2.
10. Wait 3 minutes then add 5ml of 3%H2O2 to each tube.
11. Wait 1 minute for reaction to occur, then measure and record the height of the bubbles in cm.
12. Record in Table 2. Measure the radius of the test tube and record in Table 2.
This lab is borrowed from EDCC
Onion skin cells
1. Add 2 drops of iodine to the center of a glass slide. Be careful! Iodine can stain your clothes.
2. Take a small piece of onion. Use tweezers to peel off the skin from the underside (the rough, white side) of the onion. Throw the rest of the onion piece away.
3. Carefully lay the onion skin flat in the center of the slide on top of the iodine.
4. Add 2 drops of iodine to the top of the onion skin.
5. Stand a thin glass cover slip on its edge near the onion skin, next to the drop of iodine.
6. Slowly lower the other side of the cover slip until it covers the onion skin completely. If there are air bubbles, gently tap on the glass to “chase” them out.
7. Make sure the lowest power lens (the shortest lens) is in place over the stage and the microscope light is turned on. Place the slide onto the stage of the microscope.
8. Look through the eyepiece and turn the coarse focus knob (the largest knob) until an image comes into focus. It should look like a brick wall or like lizard skin.
9. Now use the fine focus knob (the smallest knob) to make the image as focused as possible.
10. In your lab notebook, draw a picture of what you see. Label the picture “Onion skin cells 40x”. Label as many parts of the cell as you can see.
11. Looking from the SIDE of the microscope, NOT through the eyepiece, rotate the lenses to the next highest powered lens (100x). If you need to, use the fine focus knob (the smallest knob) to get the image into focus. DO NOT USE THE LARGE KNOB!! You may see a small dot in the middle of each cell.
12. Again, looking from the SIDE of the microscope, rotate the lenses to the highest powered lens (400x). If you need to, use the fine focus knob (the smallest knob) to get the image into focus. You should see a dark blob in the middle of each cell.
13. In your lab notebook, draw a picture of what you see. Label the picture “Onion skin cells 400x”. Label as many parts of the cell as you can see.
14. Switch to the lowest power lens and THEN remove the slide. Set it aside for now.
Human Cheek Cells
1. Add one drop of methylene blue to the middle of a clean slide. Be careful! Methylene blue will stain your clothes and skin.
2. Use the flat side of a toothpick to gently scratch the inside of your cheek. DO NOT GOUGE YOUR CHEEK - you don’t need chunks of skin and definitely don’t want to draw blood.
3. Gently touch the toothpick to the drop of dye on the slide. Some of your cheek cells should drift off into the dye.
4. Throw the toothpick away.
5. Stand a thin glass cover slip on its edge near the drop of dye.
6. Slowly lower the other side of the cover slip until it covers the dye completely. Make sure there are no air bubbles.
7. Make sure the lowest power lens (the shortest lens) is in place over the stage. Place the slide onto the stage of the microscope.
8. Look through the eyepiece and turn the coarse focus knob (the largest knob) until an image comes into focus. It should look like scattered blobs. Move the slide around until a nice cluster of blobs moves into the center of your image.
9. Use the fine focus knob (the smallest knob) to make the image as focused as possible.
10. In your lab notebook, draw a picture of what you see. Label the picture “Human cheek cells 40x”. Label as many parts of the cell as you can see.
11. Looking from the SIDE of the microscope, NOT through the eyepiece, rotate the lenses to the 100x lens. If you need to, use the fine focus knob (the smallest knob) to get the image into focus.
12. Again, looking from the SIDE of the microscope, rotate the lenses to the 400x lens. If you need to, use the fine focus knob (the smallest knob) to get the image into focus.
13. In your lab notebook, draw a picture of what you see. Label the picture “Human cheek cells 400x”. Label as many parts of the cell as you can see.