How Breath Alcohol Analysis Works

Alcohol shows up in the breath because it gets absorbed from the mouth, throat, stomach and intestines into the bloodstream. Alcohol­ is not digested upon absorption, nor chemically changed in the bloodstream. As blood circulates through the lungs, some of the alcohol moves across the membranes of the lung’s alveoli, into the air stored within the lungs. Because the alcohol concentration in the breath is related to the concentration in the blood, an approximate measurement can be identified when using a simple ratio formula of breath alcohol to blood alcohol which is 2100:1. This means that 2100 milliliters of alveolar air will contain the same amount of alcohol as 1 milliliter of blood

The Reason it is Impossible to Store, Purchase, and/or Sell Live Tuna

It is virtually impossible to store, purchase, and/or sell tuna fish live as tuna die shortly after capture. This is due to the fact that tuna breathe using ram-gill ventilation, which means that they must constantly stay in motion to have water pass over their gills and feed their body with oxygen. Motion is required continuously, exerted during both hours spent awake and time spent asleep. As the tuna is in motion, water flows into its mouth and over its gills and gill filaments, diffusing oxygen into the tunas bloodstream while simultaneously releasing carbon dioxide. This function is performed equally well at both slow and high rates of speed as long as consistent motion is achieved

The Fallacy of Transgender Female Athletes Competing at the Same Biological Level as Cisgender Female Athletes

It is a common misconception that transgender athletes who transition from male to female have the same sexual dimorphisms and therefore the same athletic capabilities and baseline statistics as cisgendered women when competing within athletic competition. Cisgender males on average have 40% more upper body muscle/strength than cisgendered women and 30% more lower body muscle/strength than cisgendered women, although these are mere approximations which span the entire world population which is why this is not always the case. Female hormones can reduce these advantages by 5% – 10% within the human body of elite athletes, but it is at the current time, as of 2023, impossible to completely reverse the advantage of biological male puberty for transgender male to female athletes. Surprisingly, hormone therapy rapidly reduces hemoglobin levels to that of cisgender women however all other baseline statistics remain relatively the same post transition when using hormone replacement therapy. Even after 36 months of treatment, virtually all other baseline levels are higher than the average cisgender female. These discoveries suggest that physical strength may be preserved in transgender women during the first 3 years of hormone replacement therapy. It should be noted, if the athlete does not go through male puberty, these male hormone induced advantages do not apply. This is because these traits are largely associated with testosterone but not entirely

The Origin of the Use of Analgesia While Giving Birth

Analgesia was not an option while giving birth until the mid 19th century as pain was believed to be a crucial part of the birthing experience. In 1591, Euphemia Maclean, a woman from Edinburgh, Scotland requested analgesia during the birth of her twins and was burned at the stake for this request. Analgesia started with Queen Victoria who used chloroform for the birth of her 8th child Leopold. It was Victoria’s experience that she told to others which made the practice catch on so quickly as Victoria felt that analgesia was an amazing invention which helped her immensely. In the 1950’s, the no medication approach swung back into fashion with Dr. Grantly Dick-Read, the first modern physician to suggest against analgesia as he believed the pain of childbirth to be psychological

Botulism Toxin (Botox) Disabling Portions of the Human Brain Related to Emotion

Because human beings interpret emotions by mirroring one another, botulism toxin, more commonly referred to by the brand name “Botox”, when injected into the forehead, alters brain activity connected with various emotional states. The temporary paralysis of facial muscles from the use of Botox disables a person’s ability to mirror the person(s) they are interacting with. It also hinders their ability to read and interpret the facial expressions of others. Surprisingly, this information is being leveraged within studies of depression and patients diagnosed with borderline personality disorder, as it is believed that temporary paralysis of the forehead may help aid those who are experiencing clinical depression and/or a borderline personality disorder

The Negative Effects Associated With Condom Usage During Sexual Intercourse

Many experts feel as though they cannot talk about the negative aspects of condom usage to promote safe sexual intercourse, however scientifically speaking, there are several negative effects which can be incurred when doing so. The reason these individuals with specific expertise in sexual reproduction, biology, anatomy, and/or physiology do not discuss these issues is because of the fear of spreading misinformation because it’s already difficult to get people to consistently use prophylactics during intercourse, dumping negative information into the public would most likely if not most definitely cause adherence statistics to plummet. With that being said, condom usage can and does on occasion cause 3 different bacterial strains to become present within the vagina, causing erythema both inside the vagina and upon the vulva. The infection is more likely to occur after intercourse has commenced. This rational argument is the most widely used argument within the adult entertainment industry to avoid condoms by performers both male and female. These individuals are tested monthly, sometimes even biweekly for every known kind of sexually transmitted infection and disease, which is why many within the field argue that condoms are an unnecessary risk for them to partake in as their ability to perform sexual acts is their primary source of income and if this is hindered, the consequences could be financially detrimental

The Test Subject and Scientific Experiment Which Proved the Fear Response in Human Beings Does Not Solely Reside Within the Amygdala

Justin Feinstein is one of the few scientists who have been able to study a woman who has zero fear response. To protect the woman’s identity, this subject is known only as “S.M.”, and Feinstein has had the opportunity to work with her under laboratory conditions and in real world scenarios (e.g. coffee meeting, sporting event, professional conference etc.) for the past 15 years as of 2018. S.M.’s lack of fear has had unexpected consequences within her life, as she displays no sense of typical fear induced scenarios (e.g. personal space, feeling completely comfortable being nose to nose with a complete stranger as the concept of personal space and discomfort has no meaning), heightened by the fact that S.M. does not produce typical signals of distrust when interacting with a novel person. S.M. lacks fear because she is without her amygdala, a physical trait observed in very few human beings, making S.M. one of the only people in the world to produce this physiology. S.M. has no amygdala because she has been diagnosed with Urbach-Wiethe Disease (pronounced “urr-bock vee-they”). The underlying etymology of Urbach-Wiethe Disease is still unknown but in patients with the condition, specific portions of the brain, in both hemispheres, can become subject to selective calcification which erodes the ability to function as designed. The amygdala acts as a sentry for potential fearful stimuli, and produces a response accordingly. The removal of or inability of the amygdala to work correctly results in a complete and total lack and/or loss of fear. This condition has caused S.M. considerable difficulty during her life as she has experienced dangerous interactions with those participating within the illicit drug trade. Upon one occasion, a stranger ran up to S.M., placed a firearm against her temple, and yelled “bang!”. Neighbors witnessed this event and notified law enforcement which puzzled S.M. as she did not view the event as dangerous or alarming and therefore did not expect to be contacted by the police. When the human body detects the intake of too much carbon dioxide, it can become pushed into a state of alarm. Feinstein wanted to better understand what would occur if he interfered with S.M.’s respiratory system, using 35% carbon dioxide during the first trial run. Feinstein found that S.M. was immediately fearful after a single intake breath, despite his original hypothesis of no fear response being observed. S.M. displayed an immediate and dramatic fear response with S.M. herself describing it as the “most intense fear ever felt” during her entire life. This single breath was revolutionary for neurology as it definitively proved that the amygdala is not the only region of the brain which controls and is related to fear

The Causation and Cure for Colorblindness

Being colorblind is more difficult than most people believe as those affected often cannot match clothing colors, tell when fruit is ripe, tell when meat is cooked, or tell when traffic lights are various colors in certain lighting conditions (e.g. flashing red being mistaken for flashing yellow). Color vision is trichromatic with 3 types of cone cells within the eyes which consist of blue, green, and red, which are sensitive to short, medium, and long wavelengths of light, with each cone permitting an observer to view approximately 100 different shades. When all shades are combined, the human eye can observe approximately 1,000,000 (1 million) different colors. Colorblindness can stem from faulty cone cells or an interruption between the pathway of the cones and the brain. Colorblindness has caused vehicular deaths due to accidents around the world which have occurred most often because a driver perceived a light as yellow when it was red in reality. Neuroscientist Professor Jay Neitz (pronounced “nites”), a color researcher at the University of Washington in the U.S. and his spouse, geneticist Maureen Neitz, have teamed up to try and cure colorblindness. Gene therapy is currently being researched around the world and scientists believe that colorblindness will be cured using gene therapy in the near future. Male squirrel monkeys are naturally red-green colorblind and gene studies have demonstrated that these monkeys can be afforded color vision after having a gene delivered into the cone cells within the eye. The gene produced transforms a subset of the green cones within the male squirrel monkeys eyes to force them to become red cones, red cones which have hijacked the squirrel monkeys neural circuitry which was previously utilized solely for blue-yellow color vision, essentially bifurcating into red-green cones and blue-yellow cones so that the monkeys examined developed full color vision like human beings as of 2019. The Neitz’s confirmed this by providing male squirrel monkeys colorblind examinations which when answered correctly, delivered a small treat of food after having undergone gene therapy. Trials in human beings have yet to start as the Neitz’s believe that this step is still a few years away, but expected to initiate during the 2020’s

A Revolutionary Breakthrough in Oncology Treatment

Cancer kills 9,000,000 (9 million) people each year and despite having searched for centuries, a cure has yet to be discovered by scientists. At the center of the immune system is the T cell, a type of leukocyte which respond against bacterial and viral infections alike in an effort to keep their host healthy and alive. T cells determine between threatening and non-threatening foreign and non-foreign bodies within a host by leveraging a molecule upon the surface of all cells referred to as the “T cell receptor”. Jim Allison was the first person to successfully isolate and purify the molecule which recognizes this lock and key model for infectious disease, auto-immune disease, and other innocuous substances within the body be they foreign or internally created. In 1987, French scientist Pierre Golstein and his team discovered a new protein upon the surface of T cells which he named “CTLA-4”. To study CTLA-4 in laboratory rats, Allison had to build and design a rat antibody, a Y shaped protein which would trigger a reaction by CTLA-4. Cancers are mutations and should in theory be visible to the immune system, which is why the scientific community has struggled with the paradox of why tumors go undetected by the immune system for decades. There is no discernible reason as to why the immune system can recognize and resist influenza or any other foreign or domestic body but not cancer. Allison theorized that tumors have evolved an ability to fool the immune system, engaging CTLA-4 which turns on the T cells response to halt its search and destroy measures. Allison hypothesized that if he inserted a Y shaped antibody to block the gap in between the tumor and T cells, the tumor would no longer have its ability to hide, a trait which has been evolved by tumor cells over hundreds of millions of years. This would allow the T cell to infiltrate, attack from within the tumor, shrink, and ultimately kill the growth. Allison spent the next decade trying to turn this revolutionary breakthrough discovery into a medication which could be provided to cancer patients. Allison found Alan Korman, a scientist creating medications for auto-immune disease which provided him with the expert he required to turn this idea into a reality. Korman was tasked with taking the CTLA-4 antibody which Allison and partner Max Krummell developed for laboratory rats, and turn it into a medication which could safely work within human beings with this medication subsequently being named “Ipilimumab” (pronounced “ipi-lim-ooh-mab”). Korman ended up collaborating with a friend from graduate school, Nils Lonberg to accomplish this task. Ipilimumab consists of an intramuscular injection into the leg and a 90 minute intravenous medication drip in comparison to chemotherapy and radiation therapy which take months of treatment to complete and have devastating effects upon overall health as both bad and good tissue are destroyed in an effort to eradicate all tumor cells. Allison’s work with laboratory rats demonstrated that with the help of this newly developed antibody, T cells gained the ability enter into tumors and expand their size in an effort to destroy them from the inside out. This means that the fact that tumors grow initially upon administration is a positive marker and indicative of the medication working as it demonstrates successful infiltration of the tumor cells themselves. Patients often report feeling better after a few treatment sessions, sometimes even a single session, despite computer tomography scans demonstrating that their tumors are growing larger, which under normal circumstances would make a patient feel worse. Some patients even noted increased improvement after having stopped the Ipilimumab treatment, with no further therapy required. On March 25, 2011, the U.S. Food and Drug Administration released approval for Ipilimumab. Ipilimumab and its successors have treated nearly 1,000,000 (1 million) patients worldwide with many of these patients achieving permanent remission which is essentially the definition of having been cured of cancer. Although these medications do not work in every single case, they have definitively demonstrated to be a miracle medication for hundreds of thousands of people thus far. After completing this revolutionary discovery, Allison was awarded the Nobel Prize in Medicine in 2018 for his series of discoveries related to T cells and their ability to halt cancer in its progression in perpetuity

The Link Between Dementia and Iron

Alzheimer's-Disease

Measuring iron in the brain is the best known way to confirm dementia without performing an autopsy after death. The brain naturally creates tiny bits of iron referred to as “magnetite”. As a human being ages, more and more iron accumulates within the brain. Too much iron however, is a hallmark of dementia. It is theorized that this overproduction of iron is actually due to external factors like pollution rather than naturally occurring phenomena. Dr. Barbara Marr, a world renowned expert and authority in respect to the measurement of metal in incredibly small particles, took thin tissue sections of affected brains obtained during autopsy and observed them under a highly resolved transmission electronmicroscope to review the particles within the neurons of the brain and found 2 different shapes of particle. The magnetite particles are beautifully crystalline, regular and geometric, whilst the opposing particles were rounded in shape, referred to as “spherls” (pronounced “sfare-alls”) or “nanospheres”, rounded in shape because they were originally molten droplets. For every 1 biologically manufactured magnetite, 100 artificially implanted foreign particles of iron are found within the brains of those affected by this condition as confirmed by a study which took place in Mexico City, Mexico. Although not definitely proven, the shape of these secondary particles is remarkably similar to that of airborne pollution, which suggests to scientists that there is a discernible correlation between the 2 types