Assessment of renal fibrosis and anti-fibrotic agents using a novel diagnostic and stain-free second-harmonic generation platform.
Bhuiyan. Sadman S; Shen. Matthew M; Chelvaretnam. Sharenya S; Tan. Andre Y AY; Ho. Gideon G; Hossain. Mohammed Akhter MA; Widdop. Robert E RE; Samuel. Chrishan S CS
Key Findings
- B7-33 (0.25 mg/kg/day) reduced renal fibrosis markers in mice with blocked ureters.
- Treatment increased the enzyme MMP‑2 and lowered its inhibitor TIMP‑1, indicating enhanced collagen breakdown.
- The HistoIndex SHG platform detected finer changes (collagen fiber thickness, count, and network pattern) that traditional stains missed.
Practical Outcomes
- For biohackers focused on kidney health, B7-33 shows promise as an anti‑fibrotic agent, but the data are limited to short‑term mouse studies. The dosage used in mice would need careful scaling and safety testing before human use. The new imaging method could eventually help track kidney health non‑invasively, but it’s not yet available for personal monitoring.
Summary
In a mouse model of kidney scarring, the peptide B7-33 (a relaxin‑like drug) helped keep the kidneys from building up too much collagen, a sign of fibrosis. The study also showed a new imaging tool can see these changes without staining tissue.
Abstract
Current histological measurement techniques for interstitial collagen, the basis of interstitial fibrosis, are semi-quantitative at best and only provide a ratio of collagen levels within tissues. The Genesis200 imaging system and supplemental image analysis software, FibroIndex from HistoIndex, is a novel, automated platform that uses second-harmonic generation (SHG) for imaging and characterization of interstitial collagen deposition and additional characteristics, in the absence of any staining. However, its ability to quantify renal fibrosis requires investigation. This study compared SHG imaging of renal fibrosis in mice with unilateral ureteric obstruction (UUO), to that of Masson's trichrome staining (MTS) and immunohistochemistry (IHC) of collagen I. Additionally, the platform generated data on collagen morphology and distribution patterns. While all three methods determined that UUO-injured mice underwent significantly increased renal fibrosis after 7 days, the HistoIndex platform additionally determined that UUO-injured mice had a significantly increased collagen-to-tissue cross reticulation ratio (all P < .001 vs sham group). Furthermore, in UUO-injured mice treated with the relaxin family peptide receptor-1 agonists, relaxin (0.5 mg/kg/day) or B7-33 (0.25 mg/kg/day), or angiotensin converting enzyme-inhibitor, perindopril (1 mg/kg/day) over the 7-day period, only the HistoIndex platform determined that the drug-induced prevention of renal fibrosis correlated with significantly reduced collagen fiber thickness and collagen-to-tissue cross reticulation ratio, but increased collagen fiber counts. Relaxin or B7-33 treatment also increased renal matrix metalloproteinase-2 and reduced tissue inhibitor of metalloproteinase-1 levels (all P < .01 vs UUO alone). This study demonstrated the diagnostic value of the HistoIndex platform over currently used staining techniques.
Study Information
pubmed
2021
10.1096/fj.202002053rrr