Zombie cells in disc

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lobelsteve

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Just in time. No need for viadisc, prp, disceel, or surgery.

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very preliminary.

mice model.



i hear the mice had issues with understanding the pain scale when asked, and it had to be adjusted to use CATS instead of BEARS and that this pain scale

1745494719767.png

(taken from etsy)


(they actually determined pain by observing things such as grip strength and tail suspension)
 
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Just in time. No need for viadisc, prp, disceel, or surgery.
Other things to keep an eye on...

Int Immunopharmacol. 2025 Jan 10:144:113700.
doi: 10.1016/j.intimp.2024.113700. Epub 2024 Dec 3.

Allogeneic platelet lysate activates the SIRT1-PINK1/Parkin pathway: A promising approach for improving mitochondrial function in an in vitro model of intervertebral disc degeneration​


Free article

Abstract​

Background: Intervertebral disc degeneration (IVDD) is a common cause of low back pain and spinal issues. Allogeneic platelet lysate (APL) is a blood product for several growth agents. However, only a few studies have revealed that APL can increase autophagy in defective mitochondria by activating the SIRT1-PINK1/parkin pathway while enhancing mitochondrial function to decrease reactive oxygen species (ROS) levels.

Objective: To elucidate the mechanism by which APL mediates mitochondrial autophagy via the SIRT1-PINK1/Parkin pathway in the treatment of IVDD in vitro.

Methods: Pure platelet-rich plasma (P-PRP) was prepared by two-step centrifugation, and APL was prepared via freeze-thaw cycles. The nucleus pulposus cells of New Zealand white rabbits were harvested and grown. After the third generation, four groups of cells were cultured: (1) control group: standard culture conditions; (2) IL-1β group: intervention; (3) APL group: 24-hour IL-1β intervention followed by 24-hour APL treatment; and (4) APL + EX527 group: SIRT1 inhibitor EX527 24-hour treatment after 24-hour IL-1β and APL treatment. After interventions, cell activity was measured by Trypan blue staining. Apoptosis was measured by flow cytometry in each group. Immunofluorescence labeling measured mitochondrial permeability, ROS, and ROS. RT-PCR evaluated autophagy and inflammation-related gene mRNA expression. Western blot analysis revealed the protein levels of these genes. Electron microscopy reveals mitochondrial autophagy.

Results: APL from P-PRP decreased ROS levels in an IVDD in vitro model, mediated autophagy in dysfunctional mitochondria, and alleviated inflammation via the SIRT1-PINK1/Parkin pathway.

Keywords: Allogeneic platelet lysate; Intervertebral disc degeneration; Platelet-rich plasma; Pyroptosis; Reactive oxygen species; SIRT1.
Copyright © 2024 The Author(s). Published by Elsevier B.V. All rights reserved.
 
well, if you take a vanilla extract pill (to get 0-vanillin) and nutella (as RG7112 is from the Nutlin family of chemicals duh), you wont need the PRP.
 
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