Flowers are restful to look at. They have neither emotions nor conflicts.
Sigmund Freud (via fyp-psychology)

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@flower-----child
Flowers are restful to look at. They have neither emotions nor conflicts.
Sigmund Freud (via fyp-psychology)
Yessssss
Tots Cool
My week has been the start of a new chapter as well as a fuck ton of brain work-let's just say. The crash is hard. But it's cool. But it's really not cool whenever you have literally just your keyboard and a blank white screen or a blank sheet of paper with an ink pen to reflect back on your progress and visual see it in writing that you've done it, cheers to a fuck yeah to a fresh start. But it's more of like a cheers to myself and a keyboard typing the letters allowing my eyes to do that mirror effect thing -which results in me consciously saying cheers, you are fucking winning. I'm just a huge bundle of weird fucking tired emotions right now with a hint of frustration and a taste of bitterness with the flow of a blessing because my weekend festivities well my Saturday festivity will be a cheers to my hard work as well as the opportunity to sneak away on my own for a few hours and get lost as I enjoy the laughs of strangers and the giggles of the tree branches as the grass slowly whispers hello to my soul. -that's really all I want. Give myself credit. Give myself some damn flowers because nobody else fucking does(besides my brother because he's a fucking boss.) buy myself my own gotdamn dinner since I have to pay for my food at the end of the dinner anyway. There's really no point in going with a guy to dinner regardless who he is if you have to "pay your way" where's the gentleman in that? Don't offer if you won't be willing to do the deed of treating me. Just saying. Since that random thought is off my chest back to this weekend. So yeah. I've been doing a lot of meditation; connecting with my soul on such a level to where I can actually say I DO DESERVE TO GIVE MYSELF THE CREDIT I DESERVE and feel confident in doing so. I've come a long pretty way in last 5/6 months if my life, of course in a forward motion only. Nothing less than the best of self motivation. Buts it's too late. Considering I have no choice but to rely on others in certain situations my options were limited and I had one or two choices. Get a single day pass or not go at all. SO of course I got the single day pass. I probably sound like such a damn brat right now, but hey I don't have anyone else to listen to these bullshit words of a cluster fuck. Again. There I go thinking it's not ok to feel my own fucking feelings. I need to get over that ASAP. So my friend, her cousin, and myself are all attending this one day of festival. We have a place to stay well an offer. But that offer got me stepping back simply because of emotions. Like what the fuck. I just don't understand why all of a sudden words like I miss you are used in such random times of the day. And since when you know. How is that even a trustworthy statement. I have trust issues and apparently a lot more. Seriously, do I sound like an ungrateful piece of shit or am I even making sense? What would be your feed back to this Nonsense aka emotional vent. My soul is just so openly willing to do and help anyone and anything out with the best intentions that whenever I post a status asking if someone has a spot for me to sleep and shower for one night only I'd expect atleast one person to say "maybe" considering I know about ten people off the top of my head who have and can make space for my 117 pound of flesh. Not everyone sees the soul in others - I totally understand now. Its totally cool.
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Spreading Zee Wings
Now you got me thinking and shit. I always said i never want to get married never want to have kids never want to invest my time into something that I assume will go wrong but honestly my heart feels the complete opposite. My heart is so warm when I think about the love of someone else being part of me. Or the investment of someone else's time consists of things to do with me. It's like I've been in only a few real boyfriend girlfriend status but they were all so different but so much the same in outcome. The outside world has a lot a lot a lot a lot a lot to do with the way I feel about letting someone be apart of my life and past certain gates and being ok with it. People get so distracted these days with a temporary feel good that the forget what actually really makes their soul feel good. I've placed myself in so many situations with a temporary good feeling that i don't pay attention to that very strong 2% of hope I have when it comes to relationships. Within the past 5 months or so I've grown to pay attention to that 2% of hope. I ask God to send me someone that he knows will be my soulmate but I feel like I've numbed myself so much that whenever God is talking to me about love or whatever it might be I only see it if it's a situation type of thing if it's just a ok I like you let's see what's up and no attention grabbing then I probably won't pay attention to it until it becomes a situation and I've told God this many of times I've also told him I might not be fully aware of that time when it does come that I will need guidance. I don't know I guess what I'm really getting as is I just started having a hope in the good feels of the what ifs with a romance type of love and you asking me about my feelings have now got me sitting in a bath tube full of bubbles smoking a joint reevaluating my heart and my voice in my head. Sorry if I woke you up I actually don't expect you to read this until tomorrow because I hope you're sleeping getting some good rest. K I think that's all.
"The dream is the small hidden door in the deepest and most intimate sanctum of the soul, which opens to that primeval cosmic night that was soul long before there was conscious ego and will be soul far beyond what a conscious ego could ever reach." •"part of the human self or soul is not subject to laws of space and time."• #soul #eyes #window #connect #purpose #loveyourself
George Da Pug
If my Pug wasn't so cute and lazy AF I would be more motivated. Geez the struggle
New areas of the brain identified where ALS-implicated gene is active
Many people who develop Motor Neuron Disease, also called Amyotropic Lateral Sclerosis (ALS), and/or Frontotemporal Dementia (FTD) have abnormal repeats of nucleotides within a gene called C9orf72 which causes neurons to die.
A team from the Department of Biology & Biochemistry at the University of Bath discovered for the first time that the C9orf72 gene is strongly expressed in the hippocampus of the mouse brain– a region where adult stem cells reside and which is known to be important for memory.
C9orf72 is also expressed at the olfactory bulb, involved in the sense of smell. Loss of smell is sometimes a symptom in FTD.
They also found that the C9orf72 protein changes from being concentrated in the cytoplasm of cells to both the cytoplasm and nucleus as the brain cortex develops, and during the development of neurons.
Dr Vasanta Subramanian, who led the study, said: “By uncovering novel sites of expression in the brain our findings provide an important resource for researchers studying animal models of C9orf72 mediated ALS and FTD.
“It is essential to know in which cell types in the nervous system the C9orf72 gene is expressed and where within the cell the C9orf72 protein is present.
“Our hope is that by researching accurate animal models of these diseases scientists can eventually develop new treatments and eventually cures for these devastating degenerative diseases.”
The researchers, Ross Ferguson, Eleni Serafeimidou- Pouliou and Vasanta Subramanian, were working to map expression of C9orf72 in developing and adult mouse brains to help characterise reliable animal models to study the gene and its effects in both kinds of neurodegenerative diseases, for which there are currently no cures.
Dr Brian Dickie, Director of Research Development at the Motor Neurone Disease Association, said: “It is unclear why people who carry an abnormality in genes like c9orf72 don’t usually develop symptoms of these diseases until several decades after birth, but it is possible that the activity of the gene early in life somehow ‘primes’ certain types of neuron to degenerate later in life. This detailed study provides a platform for future research to understand the role of this important gene in health and disease.”
The exact function of C9orf72 in humans and animals remains unknown, but in the mutated version in patients there are large stretches of abnormal repeated sequences.
The study is published in the Journal of Anatomy.
The findings also confirmed previous research showing C9orf72 is strongly expressed in the cerebellum and motor cortex of the brain.
Study shows exercise won’t cause you to forget things
Research has found that exercise causes more new neurons to be formed in a critical brain region, and contrary to an earlier study, these new neurons do not cause the individual to forget old memories, according to research by Texas A&M College of Medicine scientists, in the Journal of Neuroscience.
Exercise is well known for its cognitive benefits, thought to occur because it causes neurogenesis, or the creation of new neurons, in the hippocampus, which is a key brain region for learning, memory and mood regulation. Therefore, it was a surprise in 2014 when a research study, published in the journal Science, found that exercise caused mice to forget what they’d already learned.
“It stunned the field of hippocampal neurogenesis,” said Ashok K. Shetty, PhD, a professor in the Texas A&M College of Medicine Department of Molecular and Cellular Medicine, associate director of the Institute for Regenerative Medicine, and research career scientist at the Central Texas Veterans Health Care System. “It was a very well-done study, so it caused some concern that exercise might in some way be detrimental for memory.”
The animal models in the exercise group—in the previous study—showed far more neurogenesis than the control group, but contrary to what one might think, these additional neurons seemed to erase memories that were formed before they started the exercise regimen. To test this, the researchers removed the extra neurons, and the mice suddenly were able to remember again.
“The mice who exercised had a large number of new neurons,” Shetty said, “but somehow that seemed to break down the old connections, making them forget what they knew.”
Shetty and his team decided to replicate this earlier research, using rats instead of mice. Rats are thought to be more like humans physiologically, with more-similar neuronal workings. They found that—luckily for runners everywhere—these animal models showed no such degradation in memories.
“We had completely contradictory findings from the 2014 study,” said Maheedhar Kodali, PhD, a postdoctoral fellow at the Institute for Regenerative Medicine and the first author of this study. “Now we need to study other species to fully understand this phenomenon.”
Shetty and his team trained their animal models to complete a task over the course of four days, followed by several days of memory consolidation by performing the task over and over again. Then, half the trained animal models were put into cages with running wheels for several weeks, while the control group remained sedentary.
The rats who ran further over the course of that time had much greater neurogenesis in their hippocampus, and all rats who had access to a wheel (and therefore ran at least some), had greater neurogenesis than the sedentary group. On an average, they ran about 48 miles in four weeks, and neuron formation doubled in the hippocampus of these animals.
“This is pretty clear evidence that exercise greatly increases neurogenesis in the hippocampus, which has functional implications,” Kodali said. “Neurogenesis is important for maintaining normal mood function, as well as for learning and creating new memories.” This connection may help explain why exercise is an effective antidepressant.
Importantly, despite differing levels of increased neurogenesis, both moderate runners and brisk runners (those who ran further than average) in Shetty’s study showed the same ability as the sedentary runners to recall the task they learned before they began to exercise. This means even a large amount of running (akin to people who perform significant amount of exercise on a daily basis) doesn’t interfere with the recall of memory.
This new research should provide some comfort to those who read the earlier research and worried that their nightly run is causing them to forget things.
“Exercise is not at all harmful,” Shetty said. “It doesn’t cause any memory problems, and there are many studies proving its benefits for making new memories and maintaining good mood. Now, our study showed that exercise does not interfere with memory recall ability. Keep exercising, and don’t worry about losing your old memories.”
Scientists Keep a Molecule from Moving Inside Nerve Cells to Prevent Cell Death
Amyotrophic lateral sclerosis (ALS, or Lou Gehrig’s disease) is a progressive disorder that devastates motor nerve cells. People diagnosed with ALS slowly lose the ability to control muscle movement, and are ultimately unable to speak, eat, move, or breathe. The cellular mechanisms behind ALS are also found in certain types of dementia.
A groundbreaking scientific study published in Nature Medicine has found one way an RNA binding protein may contribute to ALS disease progression. Cells make RNA to carry instructions for making proteins from DNA to protein-constructing machinery.
The culprit protein, TDP-43, normally binds to small pieces of newly read RNA and helps shuttle the fragments around inside nerve cell nuclei. The study describes for the first time the molecular consequences of misplaced TDP-43 inside nerve cells, and demonstrates that correcting its location can restore nerve cell function. Misplacement of TDP-43 in nerve cells is a hallmark of ALS and other neurological disorders including frontotemporal dementia (FTD), Alzheimer’s, Parkinson’s, and Huntington’s diseases. Studies that characterize common mechanisms behind these diseases could have widespread implications and may also accelerate development of broad-based therapies.
To find the misplaced TDP-43, the researchers viewed nerve cells donated by people who died from ALS or FTD under high powered microscopes. They discovered TDP-43 accumulates in nerve cell mitochondria, critical structures responsible for generating the enormous amount of energy nerve cells require. By physically isolating the affected mitochondria the researchers were able to pinpoint TDP-43’s exact location inside the subcellular structures. They were also able to characterize variations of the protein most likely to get misplaced.
This important work was led by Xinglong Wang, PhD, from the department of pathology at Case Western Reserve University School of Medicine and a team of scientists from his laboratory.
“By multiple approaches, we have identified the mitochondrial inner membrane facing matrix as the major site for mitochondrial TDP-43,” explained Wang. “Mitochondria might be major accumulation sites of TDP-43 in dying neurons in various major neurodegenerative diseases.”
The researchers discovered that once inside the mitochondria, TDP-43 resumes its RNA binding role and attaches itself to mitochondrial genetic material. This disrupts the mitochondria’s ability to generate energy for the cell. Wang’s team was able to precisely identify the RNA in mitochondria that was bound by TDP-43 and observe the resultant disassembly of mitochondrial protein complexes. This finding provides much needed clarity on the consequences of TDP-43 misplacement inside nerve cells and opens the door for deeper studies involving a range of neurological disorders. Although the study focused on ALS and FTD, according to Wang “mislocalization of TDP-43 represents a key pathological feature correlating strongly with symptoms in more than half of Alzheimer’s disease patients.”
Mutations in the gene encoding TDP-43 have long been linked to neurodegenerative diseases like ALS and FTD. Wang’s team found that disease-associated mutations in TDP-43 enhance its misplacement inside nerve cells. The researchers also identified sections of TDP-43 that are recognized by mitochondria and serve as signals to let it inside. These sections could serve as therapeutic targets, as the study found blocking them prevents TDP-43 from localizing inside mitochondria. Importantly, Wang’s team was able to keep TDP-43 out of nerve cell mitochondria in mice using small proteins which “almost completely” prevented nerve cell toxicity and disease progression.
“We, for the first time, provide the novel concept that the inhibition of TDP-43 mitochondrial localization is sufficient to prevent TDP-43-linked neurodegeneration,” said Wang. “Targeting mitochondrial TDP-43 could be a novel therapeutic approach for ALS, FTD and other TDP-43-linked neurodegenerative diseases.”
Wang has begun to develop small proteins that prevent TDP-43 from reaching mitochondria in human nerve cells, and has a patent pending for the therapeutic molecule used in the study.
There is no treatment currently available for ALS or FTD. The average life expectancy for people newly diagnosed with ALS is just three years, according to The ALS Association.
Cause that’s what life is about. It’s about the times where you lay in the grass next to someone you love. It’s about the color of the sky, it’s about a roaring fire on a winter eve. Everybody hurts, everybody bleeds. Everyone laughs and smiles and loves. And that’s all that it is. There is no meaning of life, it’s nothing that can be defined. It’s a matter of writing your own definition.
More relatable quotes about life here (via thelovewhisperer)
"Blessed are those that know the path out of their carnal flesh, for they shall attain intuition." #tbt #throwbackthursday #outerbodyexperience #model #photography #tylerhebertphotography #modelsofinstagram #passion #message #loveyourself #believe #winning
George Da Pug and I. Coolin. #georgedapug #pugsofinstagram #pugsofinsta #puppylove #mybestfriend #straightOG #winning
The minute you start enjoying yourself and the person who you’ve become, when you walk into a room with your head held high, the minute you wake up and are glad to be you, the possibilities and opportunities will come knocking at your door.
The most followed quotes blog on Tumblr you can relate to (via thelovewhisperer)
Where there is love there is life where there is life there is grace. This beautiful Hibiscus Flower and it's red energy is a graceful miracle to me. If I can give this pretty lady life then what else can I do? Today I am blessed and want to show off my blessings in the form of beauty. Hope all you pretty souls have a beautiful day💕🌿🌞🌙🌺🍂🍃💥 •hope it travels wide, uncertain times. listen for the miracle• 😎🤗😘 #love #life #grace #miracle #blessed #hibiscus #hibiscusflower #energy #red #mothernature #connect #loveyourself #winning