Manjistha

Rubia cordifolia
Manjistha (Rubia cordifolia) is a revered Ayurvedic herb, widely prevalent for its roots, which are known for their distinctive red pigment. Traditionally, it's claimed to balance Pitta and Kapha doshas and is commonly used for its supposed blood-purifying and skin health benefits. This climbing herb, also called Indian Madder, thrives in the Himalayas.
PLANT FAMILY
Rubiaceae (Coffee)
PARTS USED
Root, Stem, Leaves
AYURVEDIC ACTION
Pitta ↓, Kapha ↓
ACTIVE COMPOUNDS
Alizarin (1-2%)

What is Manjistha?

Manjistha, scientifically known as Rubia cordifolia, is a perennial climbing herb belonging to the Rubiaceae (coffee) family. Native to the Himalayas, this plant is characterized by its long, cylindrical roots, which are the primary part used for its distinctive red pigment and therapeutic properties.

Historically, Manjistha has been widely cultivated and utilized across various cultures, particularly in traditional medicine systems and as a natural dye. Its extensive root system allows it to thrive in diverse mountainous and hilly regions.

Other Names of Manjistha

  • Indian Madder
  • Manjith
  • Manjishta
  • Rubia
  • Munjistha

Benefits of Manjistha

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<h3> Absolute Contraindications of Manjistha </h3> <h4>Concurrent anticoagulant or antiplatelet therapy / bleeding disorders [If you are on blood thinners or bleed easily]</h4> <ul> <li>🩸</li> <li>Recommendation: Avoid taking Manjistha supplements or extracts while on prescription anticoagulants (e.g., warfarin) or if you have an active bleeding disorder unless supervised by a clinician.</li> <li>Reasoning: Laboratory and animal studies of Manjistha fractions show inhibition of platelet aggregation (notably PAF-induced aggregation) and anti-thrombotic activity; combining this with anticoagulant/antiplatelet drugs could increase bleeding risk.</li> <li>Scientific_Study_Title: Anti-platelet activating factor property of Rubia cordifolia Linn.</li> <li>Scientific_Study_Authors: Y B Tripathi, S Pandey, S D Shukla</li> <li>Scientific_Study_Link: https://pubmed.ncbi.nlm.nih.gov/8406601/</li> <li>Scientific_Study_Excerpt: <p>Paraphrased summary: In experimental work using rabbit platelets, a partially purified fraction of Rubia cordifolia inhibited platelet aggregation that was triggered by platelet-activating factor (PAF), and reduced PAF binding to platelets in a dose-dependent manner. The preparation did not inhibit thrombin-induced aggregation, suggesting a selective effect on the PAF pathway. The authors concluded that R. cordifolia contains constituents that block or desensitize PAF responses, supporting an antiplatelet mechanism that could theoretically enhance bleeding in patients already taking blood thinners or with bleeding tendencies.</p> </li> </ul> <h4>Active bleeding (e.g., heavy menstrual bleeding, hemorrhage) [If you are actively bleeding]</h4> <ul> <li>🧾</li> <li>Recommendation: Do not use Manjistha during active hemorrhage or unexplained heavy bleeding; seek medical care first.</li> <li>Reasoning: Preclinical models show anti-thrombotic and platelet-modulating effects which could impede normal clot formation and prolong bleeding during active hemorrhage.</li> <li>Scientific_Study_Title: Anti-thrombotic and pro-angiogenic effects of Rubia cordifolia extract in zebrafish</li> <li>Scientific_Study_Authors: Wen M, et al. (authors listed in PubMed entry)</li> <li>Scientific_Study_Link: https://pubmed.ncbi.nlm.nih.gov/29126989/</li> <li>Scientific_Study_Excerpt: <p>Paraphrased summary: In zebrafish models of induced thrombosis, Rubia cordifolia extracts reduced thrombus formation and demonstrated dose-dependent anti-thrombotic effects while also promoting angiogenesis. Gene expression analysis indicated effects on vascular and coagulation-related markers (e.g., vWF, VEGF-A). The paper interprets these findings as demonstrating an ability of the extract to reduce clotting in vivo in this model, implying caution where intact clot formation is clinically necessary (for example, during active bleeding).</p> </li> </ul> <h4>Pregnancy and breastfeeding [If you are pregnant or nursing]</h4> <ul> <li>🤰</li> <li>Recommendation: Avoid Manjistha during pregnancy and breastfeeding due to insufficient and conflicting safety data; consult your obstetrician before any herbal use.</li> <li>Reasoning: Traditional uses include gynecological indications, and modern reviews note wide use for menstrual and uterine conditions but emphasize scarce clinical safety data - a precautionary approach is standard when safety in pregnancy is not established.</li> <li>Scientific_Study_Title: A comprehensive review of Rubia cordifolia L.: Traditional uses, phytochemistry, pharmacological activities, and clinical applications</li> <li>Scientific_Study_Authors: Wen M, Chen Q, Chen W, Yang J, et al.</li> <li>Scientific_Study_Link: https://pubmed.ncbi.nlm.nih.gov/36160419/</li> <li>Scientific_Study_Excerpt: <p>Paraphrased summary: This systematic review summarizes traditional and modern uses of Rubia cordifolia, noting broad application in gynecological disorders (abnormal uterine bleeding, dysmenorrhea) and blood-related conditions. However, the authors highlight that most pharmacological evidence is preclinical and that clinical safety, pharmacokinetics, and toxicity studies are limited or lacking. Because of the combination of traditional reproductive-system activity and sparse human safety data, the review supports caution and avoidance in pregnancy and lactation until more evidence is available.</p> </li> </ul> <h3> Relative Contraindications of Manjistha </h3> <h4>Severe liver disease or impaired liver function [If you have known liver failure or severe chronic liver disease]</h4> <ul> <li>⚠️</li> <li>Recommendation: Use only with specialist supervision; many studies suggest hepatoprotective potential but isolated reports show extracts (particularly non-root parts/fruit) may affect liver parameters - avoid unsupervised use in severe hepatic impairment.</li> <li>Reasoning: Some experiments show protective effects in toxin models, while others (fruit extract studies) reported changes in liver biomarkers and histology in animal tests, so clinical risk in advanced liver disease cannot be excluded.</li> <li>Scientific_Study_Title: Toxicity study of dibutyl phthalate of Rubia cordifolia fruits: in vivo and in silico analysis</li> <li>Scientific_Study_Authors: (authors as listed on PubMed entry)</li> <li>Scientific_Study_Link: https://pubmed.ncbi.nlm.nih.gov/25926096/</li> <li>Scientific_Study_Excerpt: <p>Paraphrased summary: An experimental study on crude ethanolic extracts of R. cordifolia fruits in mice found no acute mortality at tested doses but reported statistically significant differences in body weight and changes in biochemical markers including ALT, total protein and triglycerides; histopathological liver changes were also observed relative to controls. The authors note potential toxic constituents (e.g., dibutyl phthalate identified in fruit) and recommend careful evaluation of long-term safety, especially for formulations including non-root parts.</p> </li> </ul> <h4>Long-term, high-dose use (concern for carcinogenic potential) [If considering prolonged high-dose therapy]</h4> <ul> <li>⚠️</li> <li>Recommendation: Avoid prolonged high-dose self-administration; prefer standardized short courses and professional monitoring.</li> <li>Reasoning: Some purified constituents (rubiadin, alizarin) have been associated with preneoplastic and neoplastic lesions in long-term rodent bioassays, suggesting caution with chronic high exposure.</li> <li>Scientific_Study_Title: Carcinogenic potential of alizarin and rubiadin, components of madder color, in a rat medium-term multi-organ bioassay</li> <li>Scientific_Study_Authors: Kaoru Inoue, Midori Yoshida, Miwa Takahashi, Hitoshi Fujimoto, Makoto Shibutani, Masao Hirose, Akiyoshi Nishikawa</li> <li>Scientific_Study_Link: https://pubmed.ncbi.nlm.nih.gov/19793347/</li> <li>Scientific_Study_Excerpt: <p>Paraphrased summary: In a medium-term rat carcinogenesis bioassay, dietary exposure to rubiadin (and to a lesser extent alizarin) produced increased atypical renal tubules, renal adenomas and carcinomas, and preneoplastic lesions in liver and large intestine at higher concentrations. The investigators concluded that rubiadin has carcinogenic potential in this rodent model, which raises concern about prolonged high-level exposure to certain anthraquinone constituents found in related Rubia species.</p> </li> </ul> <h4>Concurrent use with NSAIDs (analgesics) - monitor closely [If you take NSAIDs regularly]</h4> <ul> <li>💊</li> <li>Recommendation: Discuss with your clinician before combining; monitoring for enhanced analgesic or side effects may be warranted.</li> <li>Reasoning: Preclinical work indicates that Rubia cordifolia extracts can potentiate the analgesic/anti-inflammatory actions of NSAIDs in animal models, which may alter drug effect profiles.</li> <li>Scientific_Study_Title: Variable potentiation of analgesic anti-inflammatory activity of diclofenac by two medicinal plants Rubia cordifolia and Cassia fistula in Wistar albino rats</li> <li>Scientific_Study_Authors: Rajashekar Y. R., Shobha S. N.</li> <li>Scientific_Study_Link: https://www.ijbcp.com/index.php/ijbcp/article/view/1477</li> <li>Scientific_Study_Excerpt: <p>Paraphrased summary: In rodent models, co-administration of Rubia cordifolia root preparations with sub-anti-inflammatory doses of diclofenac altered pain and inflammation outcomes compared to diclofenac alone, indicating a variable potentiation effect. The authors observed changes in pain response times and edema measures, suggesting that Rubia cordifolia may influence the pharmacodynamic profile of NSAIDs in experimental systems and supporting caution when combining in humans until clinically studied.</p> </li> </ul>

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<h4>Increased bleeding tendency / easy bruising</h4> <ul> <li>🩹</li> <li>Side effect summary: Manjistha can reduce platelet aggregation and has antithrombotic activity in preclinical studies; in sensitive people or with blood-thinning medicines this may lead to more bleeding or bruising.</li> <li>Recommendation: Stop Manjistha and consult a clinician if you develop unexplained bruising, prolonged bleeding, or if you are on anticoagulants/antiplatelets.</li> <li>Reasoning: Experimental data show inhibition of PAF-induced platelet aggregation and decreased thrombus formation in animal models, a plausible mechanism for clinically relevant bleeding when combined with other factors.</li> <li>Severity Level: Moderate</li> <li>Scientific_Study_Available: Yes</li> <li>Scientific_Study_Title: Anti-platelet activating factor property of Rubia cordifolia Linn.</li> <li>Scientific_Study_Authors: Y B Tripathi, S Pandey, S D Shukla</li> <li>Scientific_Study_Link: https://pubmed.ncbi.nlm.nih.gov/8406601/</li> <li>Scientific_Study_Excerpt: <p>Paraphrased summary: In vitro studies on rabbit platelets showed that a partially purified fraction of Rubia cordifolia inhibited platelet aggregation caused by platelet-activating factor (PAF), and reduced radiolabeled PAF binding in a dose-dependent manner. The study suggests a selective blockade of the PAF pathway, supporting a mechanistic explanation for increased bleeding risk when platelet function is already compromised or when co-administered with blood-thinning medications.</p> </li> </ul> <h4>Gastrointestinal changes and effects on gut microbiota (bloating, altered stools)</h4> <ul> <li>🦠</li> <li>Side effect summary: Short-term human supplementation studies report changes in gut microbiota composition and, in some users, mild GI symptoms such as altered stool consistency or gas.</li> <li>Recommendation: If you notice persistent GI upset, stop and consult a clinician. For short-term mild symptoms, lower the dose or take with food; for severe symptoms seek medical advice.</li> <li>Reasoning: A randomized, placebo-controlled pilot trial in healthy adults showed Manjistha (2,000 mg/day) changed fecal microbial communities over 4 weeks; individualized responses were common and some participants may experience GI side effects from microbiome modulation.</li> <li>Severity Level: Mild</li> <li>Scientific_Study_Available: Yes</li> <li>Scientific_Study_Title: Modulatory Effects of Triphala and Manjistha Dietary Supplementation on Human Gut Microbiota: A Double-Blind, Randomized, Placebo-Controlled Pilot Study</li> <li>Scientific_Study_Authors: Christine T Peterson, Aunna Pourang, Simran Dhaliwal, et al.</li> <li>Scientific_Study_Link: https://pubmed.ncbi.nlm.nih.gov/32955913/</li> <li>Scientific_Study_Excerpt: <p>Paraphrased summary: In a 4-week randomized double-blind pilot trial, healthy adults given 2,000 mg/day of Manjistha showed individualized changes in fecal microbial communities compared to placebo, including trends in Firmicutes:Bacteroidetes ratios and increased relative abundance of Akkermansia muciniphila in some participants. While no uniform adverse events were reported, the study demonstrates that Manjistha influences gut ecology, which can translate into mild, person-specific GI effects in practice.</p> </li> </ul> <h4>Potential long-term carcinogenic risk (animal data)</h4> <ul> <li>⚠️</li> <li>Side effect summary: Long-term high dosing of specific anthraquinone constituents related to Manjistha has been associated with preneoplastic and neoplastic lesions in rodent studies.</li> <li>Recommendation: Avoid chronic high-dose or unsupervised long-term use; use only standardized, professionally guided preparations and consider periodic medical follow-up for prolonged use.</li> <li>Reasoning: Rodent bioassays with rubiadin/alizarin showed increased renal and hepatic preneoplastic/neoplastic lesions at higher dietary doses, indicating a carcinogenic signal in animal models for certain purified anthraquinones present in related sources.</li> <li>Severity Level: Severe</li> <li>Scientific_Study_Available: Yes</li> <li>Scientific_Study_Title: Carcinogenic potential of alizarin and rubiadin, components of madder color, in a rat medium-term multi-organ bioassay</li> <li>Scientific_Study_Authors: Kaoru Inoue, Midori Yoshida, Miwa Takahashi, Hitoshi Fujimoto, et al.</li> <li>Scientific_Study_Link: https://pubmed.ncbi.nlm.nih.gov/19793347/</li> <li>Scientific_Study_Excerpt: <p>Paraphrased summary: In a controlled rat feeding study, diets containing rubiadin produced significant increases in atypical renal tubular hyperplasias, renal adenomas/carcinomas, and preneoplastic liver and large intestine lesions at higher exposure levels. The authors concluded rubiadin contributed substantially to carcinogenic outcomes in this animal model; although extrapolation to humans is uncertain, these findings warrant prudence with long-term exposure to concentrated anthraquinone constituents.</p> </li> </ul> <h4>Liver or kidney parameter changes (reported in some animal studies)</h4> <ul> <li>🧪</li> <li>Side effect summary: Some animal toxicity studies (particularly with fruit extracts or non-standard preparations) have reported changes in liver enzymes and histology; clinical significance in humans is not well defined.</li> <li>Recommendation: If you have known liver or kidney disease, avoid unsupervised use and check liver and kidney tests if using for an extended period.</li> <li>Reasoning: In vivo animal studies using certain extracts reported altered ALT, protein, and histopathological features in liver; this suggests potential organ effects dependent on preparation and dose.</li> <li>Severity Level: Moderate</li> <li>Scientific_Study_Available: Yes</li> <li>Scientific_Study_Title: Toxicity study of dibutyl phthalate of Rubia cordifolia fruits: in vivo and in silico analysis</li> <li>Scientific_Study_Authors: (authors listed on PubMed entry)</li> <li>Scientific_Study_Link: https://pubmed.ncbi.nlm.nih.gov/25926096/</li> <li>Scientific_Study_Excerpt: <p>Paraphrased summary: Acute oral toxicity testing of crude ethanolic extracts of R. cordifolia fruit in mice showed no mortality up to tested doses, but biochemical tests revealed differences in liver-related markers (ALT, total protein) and histopathological liver changes compared with controls. The study identified dibutyl phthalate among fruit constituents and suggested the need for long-term evaluation of toxicity for non-root plant parts and certain extract types.</p> </li> </ul>

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<h4>Anticoagulants / Antiplatelet agents (e.g., warfarin, aspirin, clopidogrel)</h4> <ul> <li>Interaction_Details: Manjistha has documented antiplatelet and antithrombotic effects in laboratory and animal models; combining it with anticoagulants or antiplatelet drugs could increase bleeding risk.</li> <li>Severity: Severe</li> <li>Recommendation: Avoid concurrent use or only use under close medical supervision with frequent monitoring (for example INR checks for warfarin users).</li> <li>Scientific_Study_Available: Yes</li> <li>Scientific_Study_Link: https://pubmed.ncbi.nlm.nih.gov/8406601/</li> <li>Scientific_Study_Title: Anti-platelet activating factor property of Rubia cordifolia Linn.</li> <li>Scientfic_Study_Authors: Y B Tripathi, S Pandey, S D Shukla</li> <li>Scientific_Study_Excerpt: <p>Paraphrased summary: Experimental research on rabbit platelets indicates that Rubia cordifolia fractions inhibited platelet aggregation initiated by platelet-activating factor and reduced PAF binding in a dose-dependent fashion. Because platelet function is a key component of hemostasis, such pharmacodynamic effects present a plausible mechanism for clinically meaningful herb-drug interactions with anticoagulant or antiplatelet therapies, raising the potential for increased bleeding tendencies when combined.</p> </li> </ul> <h4>Non-steroidal anti-inflammatory drugs (NSAIDs) - example: diclofenac</h4> <ul> <li>Interaction_Details: Preclinical studies show Rubia cordifolia preparations can modify (potentiate) the analgesic/anti-inflammatory effects of diclofenac in animal models; this may alter efficacy or side effect profile.</li> <li>Severity: Moderate</li> <li>Recommendation: Consult a clinician before combining; monitoring for increased analgesic effect or adverse events (GI or renal) is advised.</li> <li>Scientific_Study_Available: Yes</li> <li>Scientific_Study_Link: https://doi.org/10.18203/2319-2003.ijbcp20170942 (journal entry)</li> <li>Scientific_Study_Title: Variable potentiation of analgesic anti-inflammatory activity of diclofenac by two medicinal plants Rubia cordifolia and Cassia fistula in Wistar albino rats</li> <li>Scientfic_Study_Authors: Rajashekar Y. R., Shobha S. N.</li> <li>Scientific_Study_Excerpt: <p>Paraphrased summary: In rat models, co-administration of Rubia cordifolia root preparation with sub-effective doses of diclofenac altered pain and inflammation endpoints relative to diclofenac alone, indicating a potentiation effect. This suggests that in humans the herb might change NSAID effectiveness and possibly influence dose-related adverse effects, so combined use should be approached carefully and under guidance.</p> </li> </ul> <h4>Cancer chemotherapy / cytotoxic agents</h4> <ul> <li>Interaction_Details: Rubia cordifolia contains bioactive compounds with anti-tumour activity in preclinical models; potential for pharmacodynamic interactions (either antagonistic or additive) with cytotoxic drugs and theoretical effects on treatment outcomes exist.</li> <li>Severity: Moderate</li> <li>Recommendation: Do not self-administer Manjistha during chemotherapy; discuss any herbal use with the oncology team because of potential interactions and effect on treatment efficacy or toxicity.</li> <li>Scientific_Study_Available: Yes (preclinical / network pharmacology evidence)</li> <li>Scientific_Study_Link: https://pubmed.ncbi.nlm.nih.gov/30816612/</li> <li>Scientific_Study_Title: Network pharmacology-based research on the active component and mechanism of the antihepatoma effect of Rubia cordifolia L.</li> <li>Scientfic_Study_Authors: (authors as listed on PubMed entry)</li> <li>Scientific_Study_Excerpt: <p>Paraphrased summary: Network pharmacology and experimental work exploring Rubia cordifolia identified multiple constituents and targets linked to antihepatoma (anti-liver cancer) activity in vitro and in vivo. While promising for drug development, these multi-target effects imply potential for pharmacodynamic interactions with standard chemotherapeutics; without human interaction studies, combining with chemotherapy is not recommended without oncologist approval.</p> </li> </ul> <h4>Cytochrome P450 mediated interactions (CYP substrates) - current evidence</h4> <ul> <li>Interaction_Details: There is limited direct evidence that Manjistha significantly inhibits or induces major human CYP isoforms; data are insufficient and mostly from other herbs or in vitro assays, so a clear prediction is not available.</li> <li>Severity: Mild</li> <li>Recommendation: Assume unknown interaction potential. If you are taking critical drugs metabolized by CYP enzymes (e.g., certain immunosuppressants, anti-epileptics), discuss with a clinician before using Manjistha.</li> <li>Scientific_Study_Available: NA (no robust direct human CYP inhibition studies for Rubia cordifolia found)</li> <li>Scientific_Study_Link: NA</li> <li>Scientific_Study_Title: NA</li> <li>Scientfic_Study_Authors: NA</li> <li>Scientific_Study_Excerpt: <p>Paraphrased summary: Systematic reviews of herb-drug interactions highlight that many potential interactions are predicted from in vitro CYP inhibition assays or animal data; for Rubia cordifolia, direct human pharmacokinetic/CYP interaction studies are sparse. Therefore, absence of evidence is not evidence of absence - caution and professional advice are recommended when using with narrow-therapeutic-index CYP-metabolized drugs.</p> </li> </ul>