sovietrx beta

bronchogen

In the wider archive
formula -
Bioregulator
Khavinson VKh · St. Petersburg Institute of Bioregulation and Gerontology · 2003
bronchogen·Bioregulator·Ala-Glu-Asp-Leu (AEDL)
What the corpus says

A four-amino-acid peptide (Ala-Glu-Asp-Leu) developed for bronchial indications. One published paper (PMID 22117547) is mapped; no PubChem entry in our records. The trail sits in the Russian short-peptide bronchial series.

mechanism confidence: medium

PubMed papers
6
in our PubMed map
Russian full-text sources
10
Russian full-text PDFs
Archive notes
4
from archive synthesis
Confidence
medium
archive rating
Research synthesis
Mechanism

Synthetic tetrapeptide Ala-Glu-Asp-Leu (AEDL). Havigan school lineage: AEDL was isolated from bronchial epithelium polypeptide fraction by chromatography-mass-spec, then synthesised. The molecular mechanism is well-characterised for this class: in human bronchial epithelial cell cultures, AEDL epigenetically regulates Ki67, Mcl-1, p53, CD79, NOS-3 protein synthesis (cell renewal) and activates differentiation genes Nkx2.1, SCGB1A1, SCGB3A2, FoxA1, FoxA2 plus mucin genes MUC4, MUC5AC, SftpA1. the exact set that goes down in chronic bronchitis. Bronchogen is effective and safe orally in chronic bronchitis remission patients, normalising pulmonary function indices. A ancillary finding: AEDL also protects tobacco callus from NaCl salinity at 10⁻⁷ M, comparable to plant-hormone-level potency.

Key findings
  1. Human bronchial epithelial cell culture: AEDL upregulates Ki67/Mcl-1/p53/CD79/NOS-3 (cell renewal), activates Nkx2.1/SCGB1A1/SCGB3A2/FoxA1/FoxA2 (differentiation) and MUC4/MUC5AC/SftpA1 (mucins). Downregulation of these same genes correlates with chronic bronchitis development (Khavinson-Ryzhak-Linkova-Ashapkin-Drobinzeva-Basharina-Vanyushkin 2014)
  2. Chronic bronchitis patients in remission: oral AEDL normalises pulmonary function indices; safe (Khavinson 2014)
  3. Tobacco sprouts + callus under NaCl salinity: AEDL at 10⁻⁷ M enhances root/hypocotyl growth, reduces ROS, increases meristem + suction zone stress resistance; epidermal cells most protected; effects comparable to plant-hormone regulatory action (Kononenko 2018. mechanistic cross-kingdom finding)
  4. Khavinson 2020 master review: bronchogen is among the synthetic tetrapeptides (with Thymogen, Vilon, Pinealon, Vesugen, Epitalon, Cardiogen) that regulate gene expression, protein synthesis, chromatin state and telomerase elongation
Evidence quality

grade: C-only (0 A / 0 B / 4 C). Gene/protein mechanism papers do not constitute clinical translation; Kononenko plant work is adjacent.

Open questions
  • Does the epigenetic regulation extend to human clinical settings beyond bronchial epithelium?
  • Why does the peptide also work in plant tissue? Sequence-agnostic chromatin interaction, or genuine plant receptor orthologue?
  • Telomerase activation claim (Khavinson 2020). is this direct or downstream of cell renewal?
  • How should the mapped Russian clinical series in chronic bronchitis be read against the denser gene-regulation cell work?

6 Russian sources synthesised · confidence: medium

Russian full-text papers (CyberLeninka) · 10

Open-access Russian academic PDFs linked where we have them.

Papers indexed on PubMed

6 total in corpus

Reviewed against the archive corpora on 2026-09-16. Source-grounded. No clinical claims. Synthesis prose may preserve published experimental context from papers; that is research history, not a recommendation.

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