Auralune
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auraluneaudio.bsky.social
Auralune
@auraluneaudio.bsky.social
62 followers 180 following 84 posts
28 | Musician/Media composer

Non-binary Leftist

Fuck AI and fuck you if you endorse it

🔞 minors dni/dnf (I reskeet nsfw artists occasionally)

Free all occupied nations | Land back now!
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auraluneaudio.bsky.social
It seems to unfortunately be a pretty universal experience that the price of living with any sort of normalcy while taking these medications generally is either sacrificing any semblance of joy and motivation from oneself or existing in a near comatose state.
December 30, 2025 at 8:59 PM
Reposted by Auralune
zestydoesthings.bsky.social
Versions of these Gen-Ai infographics with Alt-text for better legibility!
A text based image displaying the following: GEN-AI IS THEFT Generative Ai models such as chatgpt, sora and midjourney steal from artists/photographers/ writers/translators/3d modelers and uses millions of creator's work without permission. ANY use of gen-ai in any creative industry is denying a skilled creator a job. There is NEVER an ethical excuse for using generative Ai A text based image displaying the following: GEN-AI IS WRONG Not only is it morally and ethically wrong, gen- ai responces often include incorrect information or fabricated truths. Photos created via gen-ai are becoming increasingly more difficult to spot, leading to potentially dangerous misinformation. There is NEVER an ethical excuse for using generative Ai A text based image displaying the following: GEN-AI IS DEATH Generative Ai models use an incredible amount of energy to answer a single question or generate one image. Ai data centres require a lot of electricity and water to cool down the hardware and they also produce a lot of electronic waste. This is having a detrimental effect on our environment, effecting us and our plant's wildlife. Sources- MIT, UNEP There is NEVER an ethical excuse for using generative Ai A text based image displaying the following: GEN-AI IS RACIST Gen-ai data centres are primarily built in BIPOC and low-income communities, exposing them to harmful waste and increasing electricity costs. This is by choice. Gen-ai data sets have been shown to express a bias against non-white communities. Sources- Project Muse, CapitalBNews, Harvard.edu There is NEVER an ethical excuse for using generative Ai
December 29, 2025 at 3:55 PM
Reposted by Auralune
mahtowin1.bsky.social
#WoundedKnee is the most famous US mass slaughter of Native people, but massacres happened all the time as settlers stole land. To think that Wounded Knee was an aberration is to deny the inherent & constant violence of settler colonialism.
You can see it happening in Palestine right now.
December 29, 2025 at 10:43 PM
Reposted by Auralune
sailorrooscout.bsky.social
In preclinical models, treatment repaired brain pathology, restored cognitive function, and normalized Alzheimer’s biomarkers (in HUMAN models as well).
• case.edu/news/new-stu...

The study has been published in Cell. YES, it is PEER-REVIEWED.
• www.cell.com/cell-reports...

🧪🧵⬇️
Highlights •Severity of Alzheimer's disease (AD) correlates with NAD+ homeostasis dysregulation •Preserving brain NAD+ homeostasis prevents AD in mice • Restoring brain NAD+ homeostasis reverses advanced AD in mice • Multiomics across human and mouse AD brain identifies nodes for human AD reversal Summary Alzheimer's has long been considered irreversible, but new research challenges that assumption. Scientists discovered that severe drops in the brain's energy supply help drive the disease-and restoring that balance can reverse damage, even in advanced cases. In mouse models, treatment repaired brain pathology, restored cognitive function, and normalized Alzheimer's biomarkers. The results offer fresh hope that recovery may be possible. Abstract Alzheimer's disease (AD) is traditionally considered irreversible. Here, however, we provide proof of principle for therapeutic reversibility of advanced AD. In advanced disease amyloid-driven 5xFAD mice, treatment with P7C3-A20, which restores nicotinamide adenine dinucleotide (NAD+) homeostasis, reverses tau phosphorylation, blood-brain barrier deterioration, oxidative stress, DNA damage, and neuroinflammation and enhances hippocampal neurogenesis and synaptic plasticity, resulting in full cognitive recovery and reduction of plasma levels of the clinical AD biomarker p-tau217. P7C3-A20 also reverses advanced disease in tau-driven PS19 mice and protects human brain microvascular endothelial cells from oxidative stress. In humans and mice, pathology severity correlates with disruption of brain NAD+ homeostasis, and the brains of nondemented people with Alzheimer's neuropathology exhibit gene expression patterns suggestive of preserved NAD+ homeostasis. Forty-six proteins aberrantly expressed in advanced 5xFAD mouse brain and normalized by P7C3-A20 show similar alterations in human AD brain, revealing targets with potential for optimizing translation to patient care. Graphical Abstract (CREDIT: Cell Reports Medicine)
December 28, 2025 at 5:03 PM
auraluneaudio.bsky.social
Aaaaa a lil laundry guardian 🥹❤️
December 27, 2025 at 8:32 PM
auraluneaudio.bsky.social
Quark is such a sweetie 🥺❤️
December 27, 2025 at 8:28 PM
auraluneaudio.bsky.social
He was wearing his sweater disguise 🤭❤️
December 27, 2025 at 8:02 PM
auraluneaudio.bsky.social
They are little goobers :3
December 27, 2025 at 7:49 PM