[Changes in aldosterone binding activity of kidney cytosol after stress in rats and the regulation].
Liu. D H DH; Su. Y P YP; Zhang. W W; Lou. S F SF; Gao. J S JS; Cheng. T M TM
Key Findings
- Severe scald injury reduces aldosterone binding capacity (Rt) in rat kidney cytosol.
- Mild scald injury does not significantly change aldosterone binding.
- Administration of KPV peptide prevents the injury‑induced drop in aldosterone binding, comparable to anti‑TNF/IL‑1 antibodies and alpha‑MSH.
Practical Outcomes
- KPV shows anti‑inflammatory properties that can protect kidney hormone signaling under extreme stress in rats. While promising, the data are from an animal model of severe burns and do not directly translate to human dosing or performance benefits. Biohackers might view KPV as a candidate anti‑inflammatory peptide, but more human research is needed before incorporating it into longevity or health protocols.
Summary
In rats that suffered severe burns, the amount of aldosterone that could bind to kidney cells dropped, which could affect fluid balance and blood pressure. Giving the anti‑inflammatory peptide KPV (Ac‑D‑Lys‑L‑Pro‑D‑Val) helped keep the aldosterone binding levels normal, similar to other anti‑inflammatory agents like anti‑TNF antibodies and alpha‑MSH.
Abstract
To observe the changes in aldosterone binding activity of kidney cytosols after pathological stress in rats and the regulation, binding capacity (Rt) and apparent dissociation constant (Kd) of aldosterone binding activity of kidney cytosols in normal, low-degree or heavy-degree scalded rats were measured by radioligand binding assay using [3H]aldosterone as the ligand. Changes in Rt and Kd of aldosterone binding activity were observed after injection of anti-rat TNF alpha and IL-1 beta antibodies, alpha-melanocyte-stimulating hormone (alpha-MSH) and KPV peptide (Ac-D-Lys-L-Pro-D-Val). The results indicated that there were two types of aldosterone binding activities in kidney cytosol with different Rt and Kd, and the Rt of heavy-degree scalded rats (Rt1: 22.4 +/- 5.4 fmol/mg pro, Rt2: 196.3 +/- 32.5 fmol/mg pro) was lower than that of the control group (Rt1: 41.6 +/- 7.2 fmol/mg pro, Rt2: 317.6 +/- 70.0 fmol/mg pro) (P < 0.01; P < 0.01); while the Rt of low-degree scalded rats (Rt1: 41.4 +/- 5.0 fmol/mg pro, Rt2: 314.8 +/- 45.7 fmol/mg pro) was not significantly different from that of the control group (P > 0.05; P > 0.05). Injection of anti-rat TNF alpha and IL-1 beta antibodies, alpha-MSH and KPV prevented Rt of aldosterone binding activity from decrease in kidney cytosol of rats with heavy-degree scald. These findings suggest that aldosterone binding activity may be down-regulated in heavy-degree scalded rats, but it may be reversed by injection of anti-rat TNF alpha and IL-1 beta antibodies, alpha-MSH and KPV.
Study Information
pubmed
2001