Saline nasal drops and sprays showing promise in treating the common cold

Saline nasal sprays may stop children's sneezing faster

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Saline nasal sprays appear to help speed up cold recovery: In a new study, children who were given the homemade nasal spray recovered from cold symptoms like sneezing and stuffy nose two days faster than those who weren't.

More than 200 different viruses can cause cold-like symptomsTherefore, it is difficult to develop general and effective treatments that target them. As a result, most cold therapies only relieve symptoms but do not shorten the duration of symptoms.

But research increasingly suggests that saline may be the exception. Studies have shown that adults who use saline nasal drops or sprays to relieve cold symptoms: Reduces symptoms and speeds recovery and Less likely to spread infection.

now, Steve Cunningham Researchers at the University of Edinburgh in the UK tested this method on children. They asked the parents of 150 children with cold symptoms to place three drops of saline solution into their children's nasal passages at least four times a day within 48 hours of the onset of symptoms, until symptoms subsided. The water-based solution that the parents mixed themselves contained 2.6 percent salt.

Another group of 151 children received standard cold care from their parents, such as prescribing over-the-counter medicines and encouraging rest. All of the children were under the age of seven, and their symptoms were recorded by their parents.

The researchers found that children who started using the drops within 24 hours of the onset of symptoms recovered two days faster than those who never used the drops, and their families were also less likely to develop cold symptoms. But children who started using the drops later didn't get better and were less likely to spread the cold than those who never used the drops.

Cunningham, who will present his findings at the European Respiratory Society meeting in Vienna, Austria, on September 8, says that the chloride ions in saline could prompt cells to produce an antiviral substance called hypochlorous acid, though this may need to be started early in infection, before the virus can take hold, he says.

but William Shaffner Researchers at Vanderbilt University Medical Center in Tennessee are skeptical that this method will actually help cure viral infections. [evidence] They want me to believe that this is an antiviral effect, not just symptom relief,” he says.

Schaffner says the researchers could have also given another group of children regular water drops or a low-concentration saline solution, which would show whether the saline nasal spray targets the virus and speeds recovery or simply keeps mucous membranes moist to ease symptoms, he says.

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Source: www.newscientist.com

Microsoft Surface Pro 11 Review: Microsoft’s Bold Move into Arm Technology Shows Promise

The latest Surface tablet from Microsoft is expected to bring significant improvements, moving beyond just being faster, quieter, and more efficient. The key change is the switch to an Arm-based processor at its core.

This shift to Arm chips is not new for Microsoft, but this particular machine, the Surface Pro 11, has been touted as the most successful one yet, outperforming its predecessors like the Surface Pro X from 2020 and Surface Pro 9 5G from last year.

Powered by Qualcomm’s Snapdragon X chipset, the Surface Pro 11 offers improved performance and efficiency. While the new Arm chips offer advantages, there are still some compromises in terms of software and accessories.

The exterior of the new Surface Pro remains largely unchanged from its predecessor. Photo: Samuel Gibbs/The Guardian

Despite the new chip, the Surface Pro 11 retains key features that made its predecessor successful, including a robust built-in kickstand, high-quality aluminum frame, improved speakers, and faster Windows Hello facial recognition. The 13-inch OLED display on the high-end model is top-notch, offering an exceptional viewing experience.

However, the Surface Pro 11 comes at a premium price, starting at £1,049 (€1,199/$999/AU$1,899) without the keyboard. The higher-end model with an OLED screen and faster Snapdragon X Elite chip is even pricier, starting at £1,549 (€1,799/$1,499/AU$2,699).

The Flex Keyboard continues to function even when detached, offering versatility for users. Photo: Samuel Gibbs/The Guardian

The Surface Pro 11 works well as a tablet, but a detachable keyboard is essential for maximizing its potential as a laptop. Microsoft offers various keyboard options, including the high-end Flex keyboard priced at £340.

Specification

  • Screen: 13″ LCD or OLED 2880×1920 (267 PPI) 120Hz

  • Processor: Qualcomm Snapdragon X Plus or X Elite

  • RAM: 16 or 32 GB

  • Storage: 256, 512GB or 1TB

  • Graphics: Qualcomm Adreno

  • Operating System: Windows 11 Home

  • Camera: 10.5MP rear, 12.2MP front, Windows Hello

  • Connectivity: Wi-Fi 7, Bluetooth 5.4, 2 x USB-4, Surface Connect

  • Size: 287 x 209 x 9.3mm

  • Weight: 895g (without keyboard)

Snapdragon Power

The tablet includes two USB4 ports and a Surface Connect port for charging and accessories, but lacks a headphone jack. Photo: Samuel Gibbs/The Guardian

The transition to the Arm-based Snapdragon X Elite chip offers improved efficiency and performance over traditional Intel chips. Performance comparisons have shown promising results, with the Surface Pro 11 performing on par with top Intel chips and Apple’s M1.

In everyday use, the Surface Pro 11 is fast and responsive, running quietly most of the time. Battery life is comparable to its Intel-powered predecessor, lasting around 8 hours. However, under heavy workloads, the Surface Pro 11 with Snapdragon X Elite chip offers better battery life.

While many apps have been updated to work well on the new chip, there are still compatibility issues for some legacy software, resulting in slower performance. Additionally, certain Windows apps and games may not work at all on the new system, highlighting the need for further updates from software developers.

Paint’s Cocreator uses AI to enhance manual drawing, helping you turn rough outlines into impressive works of art. Photo: Samuel Gibbs/The Guardian

The Surface Pro 11 also introduces new AI tools from Microsoft, such as Paint’s Cocreator system, offering unique creative capabilities. While these features add value, some AI functions may be limited by current implementation.

Sustainability

The tablet’s removable SSD is accessible through a small door on the back. Photo: Samuel Gibbs/The Guardian

The Surface Pro 11 demonstrates Microsoft’s commitment to sustainability, with 72% recycled materials incorporated into its design, including aluminum and rare earth metals. The company also offers repair services and recycling programs for old devices, contributing to a more environmentally-friendly approach.

Price

Starting prices for the Microsoft Surface Pro 11 range from £1,049 (€1,199/$999/AU$1,899) for the base model with Snapdragon X Plus and an LCD screen. The higher-end model with Snapdragon X Elite and an OLED screen starts at £1,549 (€1,799/$1,499/AU$2,699).

Keyboard options are available starting at £139.99 (€159.99 / $139.99 / AU$239.95), with the premium Flex keyboard priced at £340.

Verdict

The Surface Pro 11 raises the bar for Arm-based Windows tablets, offering a sleek, powerful, and quiet device. However, app compatibility remains a crucial factor in determining the overall user experience.

While the performance is commendable, the Surface Pro 11 falls short in delivering promised battery life improvements. The premium features like the OLED screen and Flex keyboard come at a steep price, which may deter some potential buyers.

Although Arm chips show promise for lightweight devices, issues with app compatibility and AI features indicate that there’s still work to be done to fully embrace this technology.

Strong Points: Great 120Hz OLED screen, impressive performance, quiet operation, USB4 connectivity, high-quality build, removable SSD, easy repairability.

Cons: High price, lack of included keyboard, app and accessory compatibility issues with Arm chips, absence of USB-A port, microSD card slot, or headphone jack, underwhelming AI features.

Source: www.theguardian.com

Malaria drug shows promise in treating polycystic ovary syndrome

The malaria drug artemisinin is extracted from the plant wormwood.

Frederick J. Brown/AFP via Getty Images

A drug already used to treat malaria may also be effective in treating polycystic ovary syndrome (PCOS).

A small study of 19 women with PCOS found that the commonly used drug artemisinin improved menstrual cycle regularity and reduced high testosterone levels that are common in PCOS patients.

The underlying cause of PCOS is unknown, but it is linked to several hormonal imbalances, including excess testosterone produced by the ovaries, which can lead to symptoms like irregular menstrual periods, infertility, and increased acne and body hair.

Affected people also tend to have reduced sensitivity to insulin, the hormone that regulates sugar, which leads to weight gain and exacerbates the hormonal imbalance.

Currently, PCOS patients are treated individually depending on their symptoms, for example undergoing laser treatments to remove body hair or taking birth control pills to regularize menstruation.

While investigating the effects of various drugs on fat cells in mice, Chi Kun Tang Researchers at Fudan University in Shanghai, China, found that artemisinin reduced symptoms in mice with PCOS-like conditions.

His team then gave 19 women with PCOS artemisinin for three months and found that all of them experienced a drop in testosterone levels, and most also saw a reduction in another substance called anti-Müllerian hormone. Associated with PCOSTwelve of the participants also experienced more regular menstrual cycles after taking the drug.

In other studies using mouse and human cells, the team found that artemisinin could reduce testosterone production in the ovaries.

Stephen Franks The Imperial College London researcher says that although the 19 women had a healthy BMI on average, weight loss tends to reduce PCOS symptoms, suggesting that artemisinin may work through another mechanism: improving insulin sensitivity. “If the results are as positive in a randomized trial as they are in this pilot study, it would be exciting,” he says.

Elisabeth Stener-Victorin Researchers at the Karolinska Institutet in Stockholm, Sweden, say the fact that artemisinin is already generally safe when used to treat malaria means that it could soon be repurposed as a new treatment for PCOS.

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Source: www.newscientist.com

Uterine fluid-based organoids show promise for treating unborn fetuses

A ball of cells grown from amniotic fluid. Red indicates lung stem cells

Giuseppe Cara, Paolo di Coppi, Mattia Guerli

Babies born with serious medical conditions may one day receive better diagnosis and treatment in utero, thanks to a new technique that takes samples of cells from intrauterine fluid and grows them in dishes. It might become.

world's first, paolo de coppi Researchers at Great Ormond Street Hospital in London have shown that fetal cells from amniotic fluid can be induced to form miniature spheres of lung, kidney or small intestine tissue. They also showed that these lung organoids could help treat babies born with a sometimes fatal lung disease called congenital diaphragmatic hernia (CDH).

Although the technique has not yet been used to treat children, the results show it is possible in principle, De Coppi said. The strategy, which researchers call “personalized prenatal medicine,” can also be modified to help treat a variety of other congenital conditions.

The idea takes advantage of a recent approach in which cells in a dish are induced to grow into lentil-sized tissue organoids that take on a three-dimensional structure. These are better than standard techniques of growing cells in two-dimensional layers to capture specific aspects of the tissue in question, such as whether the tissue is healthy or growing abnormally.

The researchers now show that samples of amniotic fluid taken during pregnancy contain fetal cells that can form tissue organoids for the lungs, kidneys, and small intestine.

Studying organoids made from cells from fetuses known to suffer from congenital disorders can tell doctors exactly what form they take, how severe they are, and how they can be treated. We may be able to provide further information.

The researchers created organoids for 12 fetuses with CDH, which causes abdominal organs to push up into the chest, preventing the left lung from growing properly. This condition can be treated by pushing a balloon into the baby's lungs while the baby is in the womb to expand the lungs and improve growth.

The researchers created lung organoids from the fetuses before and after balloon treatment. They found hints that the organoids created after the treatment behaved more like healthy lung tissue than those created beforehand, suggesting that the treatment was successful.

Therefore, organoid technology can be used not only to monitor whether a treatment is effective, as doctors perform this intervention only in the most severe cases, but also to determine whether treatment is needed in the first place. You can use it.

“This has great potential for functional diagnostics,” says De Coppi. “We know how to make diagnoses based on images, but sometimes there are extensive diagnoses. [condition severity] Possible. We want to provide better prenatal diagnostic tools. ”

“If we can classify a disease as mild, moderate, or severe, that's a huge accomplishment,” he says. Cecilia Goeterstrom At Karolinska Institutet, Stockholm, Sweden.

holm schneider Researchers at Germany's Erlangen University Hospital say their approach suggests that organoids could one day be converted into mature tissue and transplanted into babies after birth, even if part of their intestine is missing, for example. ing. “If we could engineer gut-like structures for these children to use after birth, we would be in a much better position,” he says.

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Source: www.newscientist.com

CRISPR gene therapy shows promise in treating severe inflammatory conditions

New treatment cuts the gene for kallikrein, a protein involved in inflammation (illustrated)

BIOSYM TECHNOLOGIES, INC./Science Photo Library

Nine people with a rare genetic disease that causes a life-threatening inflammatory response appear to have been cured after taking part in the first trial of a new version of CRISPR-based gene therapy.

This condition, called hereditary angioedema, causes sudden swelling of tissue that affects parts of the body such as the face and throat, similar to aspects of an allergic reaction, but cannot be treated with anti-allergy drugs.

Ten people who received a one-time gene therapy administered directly into the body saw a 95 per cent reduction in the number of 'swelling attacks' in the first six months after the treatment took effect. . Since then, all but one have had no further seizures for at least a year, although one patient who received the lowest dose had one mild seizure. “This is potentially a cure,” he says Padmalal Gurugama At Cambridge University Hospital in the UK, we worked on a new approach.

Hereditary angioedema is usually caused by mutations in the gene that encodes a protein called C1 inhibitor, which is involved in suppressing inflammation, which is part of the immune response.

People with this condition may experience a sudden buildup of fluid under their skin several times a month, which is painful and can cause suffocation if it gets stuck in the throat. This attack can be caused by a virus, changes in hormone levels, or stress.

Existing drugs that can reverse attacks work by blocking another molecule involved in inflammation called kallikrein, which is made in the liver. Because people can be born without the ability to make kallikrein without adverse effects, the results suggest that it is safe to permanently block kallikrein through gene therapy, Gurgama said.

The new treatment, developed by a company called Intellia Therapeutics in Cambridge, Massachusetts, consists of genetic material designed to cut the kallikrein gene. It is encapsulated in lipid nanoparticles and taken up by liver cells. One person was treated in the UK and nine in New Zealand and the Netherlands.

An unusual feature of this therapy is that it is administered directly to humans, a method also referred to as “in vivo” delivery. “They get one infusion and that's it,” he says. julian gilmore from University College London was not involved in the study. “It's very appealing.”

So far, most other CRISPR-based gene therapies have been administered “outside the body.” This means a more complex and time-consuming procedure of taking some of a person's cells outside the body, changing the cells in a lab, and then reinjecting them.

CRISPR gene therapy is being developed for multiple genetic diseases, with the first treatments recently approved in the UK and US to help patients with two forms of genetic anemia: sickle cell disease and beta-thalassemia. Ta.

The success of the latest trial is “very exciting,” Gilmore said. Development of CRISPR-based treatments for people with various liver-related conditions, called transthyretin amyloidosis. “This technology could be applied to any disease caused by a mutant protein produced exclusively in the liver, where it is desirable to knock down that protein,” he says.

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Source: www.newscientist.com

Breakthrough App Shows Promise in Alleviating Tinnitus Symptoms

Tinnitus, a ringing in the ears, can be a debilitating problem for those who suffer from it. However, a team of researchers has discovered a potential solution to this issue.

The survey results have been published in the magazine Frontiers of audiology and otology, and an international research team can effectively reduce symptoms in just a few weeks with an app that includes sound therapy and various training courses. The study involved 30 people with tinnitus, and almost two-thirds of them experienced “clinically significant improvement” from using the app. The team will now conduct a large-scale trial in the UK in collaboration with University College London Hospital. According to Suzanne Purdy, Waipapa Taumata Rau Professor of Psychology at the University of Auckland, New Zealand, cognitive behavioral therapy is known to help people suffering from tinnitus, but it is expensive and often difficult to access.



“[The app] Cognitive behavioral therapy, mindfulness, relaxation exercises, and sound therapy can be combined to train your brain’s responses and reduce tinnitus. The sounds you perceive fade into the background and become less noticeable.”

The new app aims to tune out the sound of tinnitus, giving the mind and body tools to suppress stress hormones and responses, and reduce the brain’s tendency to focus on the sound. The Mindear app is currently available for download for Apple and Android users. Some features are free in the app, but many are locked behind a paywall after a 7-day free trial (requires a £13 monthly subscription). Another app, the sound tinnitus app, is currently undergoing clinical trials in the UK.

About 1.5 million people in Australia, 4 million in the UK and 20 million in the US suffer from severe tinnitus, according to Dr. Fabrice Bardy, an audiologist at Waipapa Taumata Rau, University of Auckland, and lead author of the study published in the journal Frontiers of audiology and otology. He adds, “One of the most common misconceptions about tinnitus is that there’s nothing you can do about it; you just have to live with it. This is simply not true. Tinnitus Support Expertise The support of professionals with knowledge and expertise can reduce the fear and anxiety associated with a healthy patient experience.”

Tinnitus itself is not a disease, but is usually a symptom of another underlying health condition, such as damage to the auditory system or tension in the head and neck. While there is no known cure for tinnitus, management strategies and techniques can help patients. For more information, please visit the provided links.

Source: www.sciencefocus.com

Psychedelic drugs show promise in treating PTSD and traumatic brain injury

Veterans saw improvement in combat-related brain injury after taking psychedelic drugs

Shutterstock / Ground Photography

The psychedelic substance ibogaine has the potential to treat chronic disorders caused by traumatic brain injury (TBI). A single dose of this drug resulted in sustained improvements in physical and social function, cognition and mood in veterans with combat-related traumatic brain injury.

“This is the first time someone has actually been able to show that there is a neurorehabilitation effect with psychedelic drugs and that there are fairly deep signs of improvement,” he says. nolan williams at Stanford University in California.

He and his colleagues recruited 30 male veterans with traumatic brain injuries to attend a treatment facility in Mexico for five days. They were each given ibogaine, a hallucinogenic substance extracted from the iboga plant, which is native to Africa. Everyone met with a therapist before and after taking ibogaine to discuss preparation for the psychedelic experience. Participants can also participate in activities such as yoga, massage, and meditation on-site.

Participants took 12 milligrams of ibogaine per kilogram of body weight and received an intravenous infusion of magnesium to prevent heart problems associated with the drug. The researchers measured participants' disability before and after treatment on a scale of 0 to 100, with higher scores indicating greater disability. At the beginning of the study, participants' average score was 30, meaning mild to moderate disability. After 4-5 days of treatment, this score dropped below 20, and after 1 month it was around 5, indicating no disability.

At least 83 percent of participants no longer met criteria for depression, anxiety, or post-traumatic stress disorder (PTSD) one month after treatment. They also saw significant improvements in processing speed, problem solving, and working memory.

However, it is unclear whether this effect is solely due to hallucinogens. “The big problem is [that] Without a control group, it will be nearly impossible to say for sure what's going on here. ” Albert Garcia Lomu at Johns Hopkins University in Maryland. He says talking to a therapist, participating in wellness activities, and even traveling may have contributed to these improvements.

But many of these variables have previously been studied as treatments for neurological diseases with little success, Williams said. He believes a series of mechanisms could explain how ibogaine can treat traumatic brain injury. For example, he says, the drug is known to increase neuroplasticity, or the brain's ability to rewire.

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Source: www.newscientist.com

Vitamin B3 Shows Promise in Treating Chronic Inflammatory Pain

Mitochondria in specific sensory neurons may be linked to chronic pain

Beast of the Beast Science / Alamy

A type of vitamin B3 called nicotinamide riboside reduces persistent pain in mice, suggesting it may also treat chronic pain in humans.

Inflammation (the body’s first line of defense against injury and pathogens) is a major cause of pain. However, some people experience continued pain even after the inflammation has subsided.

To understand why, Niels Eichelkamp and colleagues from Utrecht University in the Netherlands analyzed the effects of inflammation on mitochondria, the powerhouses of cells. Previous research has linked chronic pain to mitochondrial dysfunction, particularly in specialized nerve cells called sensory neurons that sense changes in the environment.

The researchers injected a substance that causes inflammation into the hind legs of 15 mice. They then measured the amount of oxygen consumed by the mitochondria in the animals’ sensory neurons, which indicates mitochondrial function. They found that a week after the inflammation had subsided, the mitochondria were consuming significantly more oxygen than before the injection, suggesting that the inflammation caused lasting changes in their function. Further experiments linked these mitochondrial changes to increased pain sensitivity in the rodents even after inflammation had subsided.

The researchers then analyzed molecular byproducts of chemical reactions called metabolites in the animals’ mitochondria. They compared these to mitochondrial metabolites in naive mice. caused inflammation. The researchers found that levels of nicotinamide riboside in the mitochondria of the mice’s sensory neurons were lower than expected after the inflammation subsided. This is a type of vitamin B3 that is important for mitochondrial function.

So, about a week after inducing inflammation in another group of 12 mice, Eichelkamp and his team gave half of them a high dose of nicotinamide riboside (500 milligrams per kilogram of body weight). administered. In comparison, her recommended daily amount of vitamin B3 for most adults is 14 milligrams and 16 milligrams. They then assessed the animals’ sensitivity to pain by measuring how quickly they removed their paws from the heat. Mice that did not receive nicotinamide riboside withdrew their paws twice as fast on average as those that did, suggesting that the supplement reduced pain.

Taken together, these findings reveal two things. One is that inflammation can impair mitochondrial function in sensory neurons, and these dysfunctions increase the risk of chronic pain even after inflammation has subsided. Second, taking nicotinamide riboside supplements may help treat this chronic pain by restoring mitochondrial function.

However, people with chronic pain should not rush to take these supplements. “[This research] Still inside the rodent. How does that translate to humans? We need to check that first,” Eikelkamp said. In clinical trials, nicotinamide riboside may be ineffective or have unintended consequences, he says.

Even if these findings apply to humans, they probably only apply to certain types of chronic pain, such as chronic inflammatory diseases, Eikelkamp says. For example, more than 20 percent A proportion of patients with rheumatoid arthritis, a chronic disease characterized by persistent joint inflammation, continue to experience pain even when inflammation levels are low. Therefore, it makes sense to test these findings in that demographic first.

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Source: www.newscientist.com