# The Chronic Elevated Consumption of Hibiscus sabdariffa Linnaeus Results in Kidney Damage Associated with Excess H2S

**Authors:** Linaloe Manzano-Pech, María Elena Soto, Vicente Castrejón-Tellez, Elizabeth Soria-Castro, Verónica Guarner-Lans, Sara Caballero-Chacón, Raúl Martínez-Memije, Juan Carlos Torres-Narváez, Mohammed El-Hafidi, Israel Pérez-Torres

PMC · DOI: 10.3390/ijms27052190 · International Journal of Molecular Sciences · 2026-02-26

## TL;DR

Chronic consumption of Hibiscus sabdariffa infusion increases hydrogen sulfide in the kidneys, leading to damage.

## Contribution

This study shows that long-term Hibiscus sabdariffa intake causes kidney damage through elevated H2S levels.

## Key findings

- Chronic HSL consumption increases H2S and reduces renal vasodilatation and OXPHOS.
- Elevated CBS and CSE activity from HSL leads to kidney damage.
- GSH/GSSG ratio and NrF2 expression are increased in HSL-treated rats.

## Abstract

Hydrogen sulfide (H2S) is essential for renal function; however, it is toxic at high concentrations. H2S is increased during reductive stress (RS). Increased antioxidant capacity and reduced/oxidized glutathione (GSH/GSSG) characterize a rat model of RS associated with chronic consumption of 6% Hibiscus sabdariffa Linnaeus (HSL). Here, we evaluate if chronic consumption of an infusion of HSL causes kidney damage associated with an increase in H2S. Twenty-one Wistar rats were divided into three groups. Group 1: rats received plain tap water ad libitum (G1); Group 2: rats received an ad libitum infusion of 6% HSL for one month (G2); and Group 3: rats consumed a 6% HSL infusion for one month and were then given natural water for another month (G3). We evaluated renal vasodilatation, cystathionine–β–synthase (CBS), cystathionine–γ–lyase (CSE), 3–mercaptopyruvate-sulfur-transferase (3–MST), γ-glutamylcysteine synthetase (GCLC), Nrf2, total OXPHOS, H2S concentration, GSH/GSSG and oxidized/reduced thiols in the kidney. Renal vasodilatation and total OXPHOS in complex IV and I and oxidized/reduced thiols were decreased (p ≤ 0.01) but H2S, CBS, SCE, GCLC, and NrF2 expression and GSH/GSSG were increased (p ≤ 0.04). The HSL infusion provided cysteine that was metabolized by CBS and CSE, elevating chronic H2S and favoring renal damage.

## Linked entities

- **Genes:** CBS (cystathionine beta-synthase) [NCBI Gene 875], CTH (cystathionine gamma-lyase) [NCBI Gene 1491], GCLC (glutamate-cysteine ligase catalytic subunit) [NCBI Gene 2729], GABPA (GA binding protein transcription factor subunit alpha) [NCBI Gene 2551]
- **Proteins:** GABPA (GA binding protein transcription factor subunit alpha)
- **Chemicals:** Hydrogen sulfide (PubChem CID 402), H2S (PubChem CID 402), glutathione (PubChem CID 124886), GSH/GSSG (PubChem CID 86619103)

## Full-text entities

- **Genes:** Mpst (mercaptopyruvate sulfurtransferase) [NCBI Gene 192172] {aka Mst}, Gclc (glutamate-cysteine ligase, catalytic subunit) [NCBI Gene 25283] {aka Glclc}, Nfe2l2 (NFE2 like bZIP transcription factor 2) [NCBI Gene 83619], Cbs (cystathionine beta synthase) [NCBI Gene 24250], Cth (cystathionine gamma-lyase) [NCBI Gene 24962] {aka CGL, CSE}
- **Diseases:** Kidney Damage (MESH:D007674)
- **Chemicals:** H2S (MESH:D006862), thiols (MESH:D013438), GSSG (MESH:D019803), cysteine (MESH:D003545), GSH (MESH:D005978), water (MESH:D014867)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

## Full text

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## Figures

9 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12984581/full.md

## References

55 references — full list in the complete paper: https://tomesphere.com/paper/PMC12984581/full.md

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Source: https://tomesphere.com/paper/PMC12984581