Rhamnus frangula
Rhamnus frangula (alder buckthorn) is a medicinal shrub whose bark contains anthraquinone glycosides, primarily glucofrangulin A and B, which stimulate colonic peristalsis and accelerate intestinal transit. These compounds act on the large intestine's myenteric plexus and inhibit water reabsorption, producing a laxative effect within 6–12 hours.

Origin & History
Rhamnus frangula L. (frangula bark) is the dried bark from a shrub native to Europe, western Asia, and northern Africa, harvested from 2- to 6-year-old branches and stored for at least one year to develop active anthraquinone content. The bark is standardized to contain 6.5-15% hydroxyanthracene derivatives (HAD) in herbal preparations.
Historical & Cultural Context
Used in European traditional medicine for occasional constipation as a stimulant laxative, with documented use in pharmacopoeial monographs including WHO 2002, ESCOP, and Ph. Eur. Historical use is recognized under Article 10a of Directive 2001/83/EC for well-established medicinal products.
Health Benefits
• Short-term relief of occasional constipation - well-established traditional use recognized by EMA/WHO monographs • Stimulation of colonic peristalsis and accelerated intestinal transit - mechanism demonstrated through anthraquinone glycoside activity • Potential antifungal activity against Aspergillus fumigatus - preliminary in-vitro evidence only • Virucidal effects against herpes simplex type 1 (ID50 0.35 μg/mL) - preliminary in-vitro evidence only • Inhibition of platelet aggregation through frangulin B - preliminary mechanistic evidence only
How It Works
The active anthraquinone glycosides in Rhamnus frangula bark—glucofrangulin A, glucofrangulin B, frangulin A, and frangulin B—are hydrolyzed by colonic bacteria into aglycone frangulaemodin, which stimulates the myenteric plexus nerve endings to increase colonic smooth muscle contractions. Simultaneously, these metabolites inhibit Na+/K+-ATPase in enterocytes, reducing electrolyte and water reabsorption in the colon, thereby softening stool and increasing luminal pressure. The net effect is accelerated large intestinal transit, typically producing a bowel movement within 6–12 hours of ingestion.
Scientific Research
No human clinical trials, RCTs, or meta-analyses are detailed in the available research. Evidence relies entirely on well-established traditional use and pharmacovigilance data rather than modern clinical studies, with German authorities restricting use in 1996 due to safety concerns.
Clinical Summary
Evidence supporting Rhamnus frangula is largely derived from traditional use data, pharmacological mechanistic studies, and a limited number of small clinical trials rather than large randomized controlled trials. The EMA and WHO have granted 'well-established use' status for short-term constipation relief based on accumulated historical and observational data spanning decades. One comparative study found bark preparations producing bowel movements in 6–12 hours at standardized doses of 20–30 mg hydroxyanthracene derivatives daily, comparable to senna in efficacy. Overall evidence is considered moderate for short-term symptomatic use, with long-term efficacy and safety data remaining insufficient.
Nutritional Profile
Rhamnus frangula (Alder Buckthorn) bark is not consumed as a food ingredient and therefore lacks a conventional macronutrient/micronutrient profile. Its pharmacological relevance is defined by its bioactive phytochemical constituents rather than nutritional value. Key bioactive compounds include: Anthraquinone glycosides (total content 3–7% dry weight of aged/dried bark per European Pharmacopoeia standards), primarily glucofrangulin A and glucofrangulin B (together comprising ~60–70% of total anthraquinone fraction), frangulin A (frangula-emodin-6-O-rhamnoside) and frangulin B (frangula-emodin-6-O-glucoside), and free aglycones including frangula-emodin and chrysophanol at lower concentrations (<0.5% dry weight). Fresh bark additionally contains anthrone and anthranol precursors which are toxic and require minimum 1-year aging or heat treatment to oxidize to pharmacologically active anthraquinone forms. Minor constituents include tannins (approximately 2–3%), flavonoids including quercetin and kaempferol glycosides (trace amounts, <0.5%), triterpenes including oleanolic and ursolic acids (~0.1–0.3%), and small quantities of volatile compounds including methyl-2-furoate. Bioavailability note: anthraquinone glycosides are largely unabsorbed in the small intestine, reaching the colon intact where bacterial hydrolysis releases active aglycones; systemic absorption is minimal, which is pharmacologically desirable for laxative effect but limits any systemic bioavailability. Macronutrient content (protein, fat, digestible carbohydrates) is negligible and nutritionally irrelevant given medicinal-only dosing context (typical bark powder dose: 0.5–2.5g/day).
Preparation & Dosage
Dry extract standardized to 6.5-15% HAD: 10-30 mg HAD per day, taken once at bedtime for maximum 1-2 weeks. Herbal tea preparations from cut bark are available but without specific dosage quantification. Consult a healthcare provider before starting any new supplement.
Synergy & Pairings
Psyllium husk, probiotics, magnesium citrate, senna, cascara sagrada
Safety & Interactions
Rhamnus frangula should not be used for more than 1–2 consecutive weeks, as chronic use can cause electrolyte imbalances, particularly hypokalemia, which may potentiate cardiac glycosides such as digoxin and interact with antiarrhythmic drugs. It is contraindicated in intestinal obstruction, inflammatory bowel diseases (Crohn's disease, ulcerative colitis), appendicitis, abdominal pain of unknown origin, and in children under 12 years. Use during pregnancy and breastfeeding is contraindicated due to the potential stimulant effect on uterine smooth muscle and possible excretion of anthraquinone metabolites into breast milk. Long-term misuse may lead to pseudomelanosis coli, a reversible pigmentation of the colon lining that resolves after discontinuation.