Researchers have created a new drug delivery system that could improve the effectiveness of an emerging concept in cancer treatment — to dramatically slow and control tumors on a long-term, sustained basis, not necessarily aiming for their complete elimination.
The approach, called a “metronomic dosage regimen,” uses significantly lower doses of chemotherapeutic drugs but at more frequent time intervals. This would have multiple goals of killing cancer cells, creating a hostile biological environment for their growth, reducing toxicity from the drug regimen and avoiding the development of resistance to the cancer drugs being used.
New research in mice may offer insight into how the Zika virus is transmitted sexually and affects a fetus. People typically get the virus through the bite of an infected mosquito, although Zika can also be spread through sex.
Since the Zika outbreak began last year in Brazil, thousands of babies whose mothers were infected with Zika early in pregnancy have been born with a devastating birth defect known as microcephaly, in which the head and brain are abnormally small.
Neuroscientists have developed a way to turn an entire mouse, including its muscles and internal organs, transparent while illuminating the nerve paths that run throughout its body.
The process, called uDisco, provides an alternate way for researchers to study an organism’s nervous system without having to slice into sections of its organs or tissues. It allows researchers to use a microscope to trace neurons from the rodent’s brain and spinal cord all the way to its fingers and toes.
“When I saw images on the microscope that my students were obtaining, I was like ‘Wow, this is mind blowing,’” said Ali Ertürk, a neuroscientist from the Ludwig Maximilians University of Munich in Germany and an author of the paper. “We can map the neural connectivity in the whole mouse in 3D.”
There’s an uncomfortable truth to modern medicine.That drug you take for your high blood pressure, the vaccine to prevent infectious disease,
the pill to avoid pregnancy, the medical ointment for your skin condition, or even the pacemaker keeping your arrhythmia in check — all of those and more have, at one time, been tested on a live animal.
Between the testing of a new chemical compound on cell cultures in a laboratory and the first time that compound is given to a live human, it will almost certainly be administered to mice, rats, rabbits and perhaps even a non-human primate.
Animal research has been credited with improving human health and leading to many medical breakthroughs. However, animal research still remains a controversial topic, with many animal rights groups believing that animal research is wasteful and pointless. One way to improve the public opinion of animal research is through education and openness. Openness can be achieved by showing the public what an animal research facility looks like and what research takes place there, in addition to discussing how that research affects human health.
In order to address the goal of transparency and openness in animal research, 72 organizations involved with bioscience in the United Kingdom (UK) launched the Concordat on Openness in Animal Research. Currently, over 100 UK organizations have signed the Concordat and pledged to “be clear about when, how and why [they] use animals in research”, “enhance [their] communications with the media and the public about [their] research using animals”, “be proactive in providing opportunities for the public to find out about research using animals”, and “report on progress annually and share [their] experiences”. The Concordat, and the new environment of openness it seeks to encourage, has led many institutions to become more open to the media.
Scientists at the Stowers Institute for Medical Research have reported a detailed description of how function-impairing mutations in polr1c and polr1d genes cause Treacher Collins syndrome (TCS), a rare congenital craniofacial development disorder that affects an estimated 1 in 50,000 live births.
Collectively the results of the study, published in the current issue of PLoS Genetics, reveal that a unifying cellular and biochemical mechanism underlies the etiology and pathogenesis of TCS and its possible prevention, irrespective of the causative gene mutation.
Harvard Stem Cell Institute (HSCI) researchers at Harvard University and the Broad Institute of Harvard and MIT have found evidence that bone marrow transplantation may one day be beneficial to a subset of patients suffering from amyotrophic lateral sclerosis (ALS), a fatal neurodegenerative disorder more commonly known as Lou Gehrig’s disease.
In the photo of the murine spleen shown, lymphoid tissue (purple) is responsible for launching an immune response to blood-born antigens, while red pulp (pink) filters the blood. Mutations in the C9ORF72 gene, the most common mutation found in ALS patients, can inflame lymphoid tissue and contribute to immune system dysfunction.
ALS destroys the neurons connecting the brain and spinal cord to muscles throughout the body. As those neurons die, patients progressively lose the ability to move, speak, eat, and breathe.
NIH-funded mouse study is the first to show that visual stimulation helps re-wire the visual system and partially restores sight.
A study in mice funded by the National Institutes of Health (NIH) shows for the first time that high-contrast visual stimulation can help damaged retinal neurons regrow optic nerve fibers, otherwise known as retinal ganglion cell axons. In combination with chemically induced neural stimulation, axons grew further than in strategies tried previously. Treated mice partially regained visual function. The study also demonstrates that adult regenerated central nervous system (CNS) axons are capable of navigating to correct targets in the brain. The research was funded through the National Eye Institute (NEI), a part of NIH.
A number of countries have ended some types of research with chimpanzees over the past decades. For example, the US National Institutes of Health announced in November 2015 that it would no longer support many types of chimpanzee research. In Europe, the fate of former research chimpanzees has depended upon a mix of private wildlife parks and zoos for the animals’ care and management. The outcomes in term of chimpanzee health and survival remain relatively unknown.
Amita Sehgal, a sleep researcher at the University of Pennsylvania, has discovered some of the key genes that control our 24-hour circadian cycle, making us fall asleep at night and rise again in the morning. Sehgal didn’t find these genes in people, however. She found them in flies.