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What has been shaping the human mind throughout the history of mankind? What is the difference between mind and consciousness? What links quantum physics to consciousness? What gives rise to our subjective experience? What drives our accelerating evolution?

If you’re eager to familiarize with probably the most advanced ontological framework to date or if you’re already familiar with the Syntellect Hypothesis which, with this series, is now presented to you as the full-fledged Cybernetic Theory of Mind, you should get this book two of the series which corresponds to Part II of The Syntellect Hypothesis: Five Paradigms of the Mind’s Evolution. This volume two contains some newly-introduced and updated material if compared with the originally published version and can be read as a stand-alone book. At the same time, it is highly recommended to obtain The Syntellect Hypothesis as the original coherent version of the same theoretical framework instead of waiting for all five books to come out and if you don’t need extra detailing.

Over the course of human history, from the first bonfire to today’s smartphones and hyperloops, we have designed tools, and tools designed us back by shaping our minds. Technology isn’t just something outside ourselves, it’s an innate part of human nature, like sex, sleeping or eating, and it has been a major driving force in evolution. Tool using, along with language, bipedalism, and cooking (quite literally) is essentially what has made us human.

From the data, the GTEx team could identify the relationship between specific genes and a type of regulatory DNA called expression quantitative trait loci, or eQTL. At least one eQTL regulates almost every human gene, and each eQTL can regulate more than one gene, influencing expression, GTEx member and human geneticist Kristin Ardlie of the Broad Institute tells Science.

Another major takeaway from the analyses was that sex affected gene expression in almost all of the tissue types, from heart to lung to brain cells. “The vast majority of biology is shared by males and females,” yet the gene expression differences are vast and might explain differences in disease progression, GTEx study coauthor Barbara Stranger of Northwestern University’s Feinberg School of Medicine tells Science. “In the future, this knowledge may contribute to personalized medicine, where we consider biological sex as one of the relevant components of an individual’s characteristics,” she says in a statement issued by the Centre for Genome Regulation in Barcelona, where some of the researchers who participated in the GTEx project work.

Another of the studies bolsters the association between telomere length, ancestry, and aging. Telomere length is typically measured in blood cells; GTEx researchers examined it in 23 different tissue types and found blood is indeed a good proxy for overall length in other tissues. The team also showed that, as previously reported, shorter telomeres were associated with aging and longer ones were found in people of African ancestry. But not all earlier results held; the authors didn’t see a pattern of longer telomeres in females or constantly shorter telomeres across the tissues of smokers as previous studies had.

Not everyone is singing the project’s praises. Dan Graur, an evolutionary biologist at the University of Houston who often criticizes big projects like GTEx, tells Science the results are hard to parse and there was little diversity, with 85 percent of the tissue donors being white. He also was critical of the use of deceased donor tissue, questioning if it truly reflects gene activity in living humans. “It’s like studying the mating behaviour of roadkill.”

Other scientists say there’s much work to be done. The gene regulation map leaves many unanswered questions about the exact sequences that cause disease and how gene regulation systems work in tandem. Genomicist Ewan Birney, the deputy director general of EMBL, tells Science, “We shouldn’t pack up our bags and say gene expression is solved.”


A decade-long effort to probe gene regulation reveals differences between males and females, points to essential regulatory elements, and offers insight into past work on telomeres.

Summary: Glial cells not only control the speed of nerve conduction, but they also influence the precision of signal transduction.

Source: University of Münster

For the brain to work efficiently, it is important that a nerve impulse arrives at its destination as quickly and as precisely as possible. It has been long been known that the nerve fibres — also known as axons — pass on these impulses. In the course of evolution, an insulating sheath — myelin — developed around the axons which increases the speed of conduction. This insulating sheath is formed by the second type of cell in the nervous system — the glial cells, which are one of the main components of the brain. If, as a result of disease, myelin is depleted, this leads to neurological disorders such as Multiple Sclerosis or Morbus Charcot-Marie-Tooth.

Cutting calories significantly may not be an easy task for most, but it’s tied to a host of health benefits ranging from longer lifespan to a much lower chance of developing cancer, heart disease, diabetes and neurodegenerative conditions such as Alzheimer’s.

A new study from teams led by Scripps Research Professors Bruno Conti, Ph.D., and Gary Siuzdak, Ph.D., illuminates the critical role that temperature plays in realizing these diet-induced health benefits. Through their findings, the scientists pave the way toward creating a medicinal compound that imitates the valuable effects of reduced body temperature.

The research appears in Science Signaling.

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Magnetism offers new ways to create more powerful and energy-efficient computers, but the realization of magnetic computing on the nanoscale is a challenging task. A critical advancement in the field of ultralow power computation using magnetic waves is reported by a joint team from Kaiserslautern, Jena and Vienna in the journal Nano Letters.

A local disturbance in the magnetic order of a magnet can propagate across a material in the form of a wave. These waves are known as spin waves and their associated quasi-particles are called magnons. Scientists from the Technische Universität Kaiserslautern, Innovent e. V. Jena and the University of Vienna are known for their expertise in the called ‘magnonics,’ which utilizes magnons for the development of novel types of computers, potentially complementing the conventional electron-based processors used nowadays.

“A new generation of computers using magnons could be more powerful and, above all, consume less energy. One major prerequisite is that we are able to fabricate, so-called single-mode waveguides, which enable us to use advanced wave-based signal processing schemes,” says Junior Professor Philipp Pirro, one of the leading scientists of the project. “This requires pushing the sizes of our structures into the nanometer range. The development of such conduits opens, for example, an access to the development of neuromorphic computing systems inspired by the functionalities of the human brain.”

For college students studying science, doing labwork as part of their classes is a vital way to learn research skills and better understand concepts from lectures.

That presents a challenge for schools that are operating remotely during the coronavirus pandemic — so some biology programs are mailing brains, eyeballs, and even entire fetal pigs to their students so they can dissect them at home.

At Lafayette College, neuroscience students enrolled in a physiology course recently received packages in the mail that contained preserved sheep brains, which are commonly chosen by schools due to their close resemblance to human brains. Then, neuroscientist and psychologist Luis Schettino — who, in the interest of transparency, was one of my professors when I attended Lafayette — guided his students over a video call as they dissected the brains.


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Dental fillings may soon be left in the ash heap of history, thanks to a recent discovery about a drug called Tideglusib.

Developed for and trialled to treat Alzheimer’s disease, last year scientists found the drug also happens to promote the natural tooth regrowth mechanism in mice, allowing the tooth to repair cavities.

Tideglusib works by stimulating stem cells in the pulp of teeth, the source of new dentine. Dentine is the mineralised substance beneath tooth enamel that gets eaten away by tooth decay.

People who were children when their parents were divorced showed lower levels of oxytocin — the so-called “love hormone” — when they were adults than those whose parents remained married, according to a study led by Baylor University. That lower level may play a role in having trouble forming attachments when they are grown.

Oxytocin — secreted in the brain and released during bonding experiences such as delivery of a baby or sexual interaction or nursing, even being hugged by a romantic partner — has been shown in previous research to be important for social behavior and emotional attachments in early life. The oxytocin system also has been linked to parenting, attachment and anxiety.

The new study, published in the Journal of Comparative Psychology, delves into an area that has not been well researched — a link between oxytocin, early experience and adult outcomes.

“Since the rates of divorce in our society began to increase, there has been concern about the effects of divorce on the children,” said lead author Maria Boccia, Ph.D., professor of child and family studies at Baylor University in the Robbins College of Health and Human Sciences. “Most research has focused on short-term effects, like academic performance, or longer-term outcomes like the impact on relationships. How divorce causes these effects, however, is unknown.

“Oxytocin is a neurohormone that is important in regulating these behaviors and is also sensitive to the impact of stressful life events in early life,” she said. “This is a first step towards understanding what mechanisms might be involved.”

Previous studies of children whose parents were divorced have found that the experience was associated with mood disorders and substance abuse — behaviors found to be related to oxytocin, Boccia said. Additionally, such childhood experiences as divorce or death of a parent are associated with depression and anxiety in adolescents and adults, as well as with poorer parenting in adulthood, less parental sensitivity and warmth, overreaction and increased use of punishment.

Researchers in the Baylor study examined the effect of the experience of parental divorce in childhood on later adult oxytocin levels. They also asked participants to complete a set of questionnaires on attachment style and other measures.

“What we found was that oxytocin was substantially lower in people who experienced parental divorce compared to those who did not and correlated with responses on several measures of attachment,” Boccia said. “These results suggest that oxytocin levels are adversely affected by parental divorce and may be related to other effects that have been documented in people who experience parental divorce.”

Scientists at Cold Spring Harbor Laboratory (CSHL) and Stanford University have pinpointed the circuit in the brain that is responsible for sleepless nights in times of stress—and it turns out that circuit does more than make you toss and turn. Their study, done in mice, ties the same neuronal connections that trigger insomnia to stress-induced changes in the immune system, which weaken the body’s defenses against a host of threats.

The study, reported September 9, 2020, in the journal Science Advances, connects and explains two familiar problems, says CSHL Assistant Professor Jeremy Borniger. “This sort of stress-induced insomnia is well known among anybody that’s tried to get to sleep with a looming deadline or something the next day,” he says. “And in the clinical world, it’s been known for a long time that chronically stressed patients typically do worse on a variety of different treatments and across a variety of different diseases.”

Like many aspects of the body’s stress response, these effects are thought to be driven by the stress hormone cortisol. Working in the Stanford lab of Luis de Lecea, where Borniger completed a postdoctoral fellowship prior to joining CSHL, the research team found a direct connection between stress-sensitive neurons in the brain that trigger cortisol’s release and nearby neurons that promote insomnia.

… The same connection, they found, also has a potent effect on the immune system. Stress significantly disrupts the abundance of certain immune cells in the blood, as well signaling pathways inside them, and the team was able to recreate these changes simply by stimulating the same neurons that link stress to insomnia.

Understanding this circuitry opens the door to a deeper understanding of the consequences of stress, not just in healthy individuals but also in disease, Borniger says:

“I’m really interested in how we can manipulate distinct circuits in the brain to control not just the immune system at baseline, but in disease states like inflammatory bowel disease or in cancer or in psoriasis—things that are associated with systemic inflammation. Because if we can understand and manipulate the immune system using the natural circuitry in the body rather than using a drug that hits certain targets within the system, I think that would be much more effective in the long run, because it just co-opts the natural circuits in the body.”