Botanical species · safety record

Cynoglossum officinale

The EFSA Compendium of Botanicals holds 19 constituent measurements and 3 adverse-effect records for Cynoglossum officinale. This page reports what those source records contain and how to reach them. It carries no effect estimate, no dose and no recommendation.

Accepted name in source: Cynoglossum officinale L.

19Constituent measurements
3Safety records
7Cited sources
0Licensed products (Canada)

Regulatory presence

No Health Canada licensed natural health product in the snapshot names this species as a medicinal ingredient under this exact binomial. Absence here means absence from this one register under this one name, not absence from trade, and not a safety verdict.

What the records describe

Constituents measured

  • Pyrrolizidine alkaloids17
  • Heliosupine2

Plant parts

  • Leaves7
  • Aerial part of plants4
  • Flower3
  • Stem3
  • stalk3
  • Live plants2
  • Fruit unspecified1
  • Roots and other underground parts1
  • Seed1

Preparations

  • Solvent extraction20
  • Drying (dehydration)1

Effect types

  • Hepatotoxicity3

Target tissues

  • Liver3

Recorded constituents

What analytical work has found in this species, at which plant part and preparation. A measured constituent is a fact about material, not about effect.

SubstancePlant partPreparationConcentrationAnalytical methodSource
HeliosupineLeavesSolvent extraction236.9 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
HeliosupineAerial part of plantsSolvent extraction287.3 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
Pyrrolizidine alkaloidsLeavesSolvent extraction≥ 224 Microgram/gramLC-MSResolve DOI
Pyrrolizidine alkaloidsFruit unspecifiedSolvent extraction0.71 PercentGC-MS (Q)Resolve DOI
Pyrrolizidine alkaloidsFlowerSolvent extraction0.98 PercentGC-MS (Q)Resolve DOI
Pyrrolizidine alkaloidsLeavesSolvent extraction≤ 9466 Microgram/gramLC-MSResolve DOI
Pyrrolizidine alkaloidsRoots and other underground partsSolvent extraction0.05 PercentGC-MS (Q)Resolve DOI
Pyrrolizidine alkaloidsLeavesSolvent extraction0.2 PercentGC-MS (Q)Resolve DOI
Pyrrolizidine alkaloidsStem / stalkSolvent extraction≥ 0.1 PercentNuclear Magnetic Resonance (NMR)Resolve DOI
Pyrrolizidine alkaloidsStem / stalkSolvent extraction0.2 PercentGC-MS (Q)Resolve DOI
Pyrrolizidine alkaloidsLeavesSolvent extraction≤ 2.12 PercentNuclear Magnetic Resonance (NMR)Resolve DOI
Pyrrolizidine alkaloidsSeedSolvent extraction1 PercentNuclear Magnetic Resonance (NMR)Resolve DOI
Pyrrolizidine alkaloidsStem / stalkSolvent extraction≤ 1.29 PercentNuclear Magnetic Resonance (NMR)Resolve DOI
Pyrrolizidine alkaloidsAerial part of plantsSolvent extraction18.55 Microgram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
Pyrrolizidine alkaloidsLeavesSolvent extraction5.48 Milligram/gramHigh Performance Liquid Chromatography (HPLC)/Liquid Chromatography (LC)Resolve DOI
Pyrrolizidine alkaloidsFlowerSolvent extraction≤ 1.36 PercentNuclear Magnetic Resonance (NMR)Resolve DOI
Pyrrolizidine alkaloidsLeavesSolvent extraction≥ 0.31 PercentNuclear Magnetic Resonance (NMR)Resolve DOI
Pyrrolizidine alkaloidsFlowerSolvent extraction≥ 0.12 PercentNuclear Magnetic Resonance (NMR)Resolve DOI
Pyrrolizidine alkaloidsAerial part of plants≥ 1.6 PercentUnspecifiedNo resolvable identifier

Recorded adverse effects

Adverse effects reported in the source literature, most often in animal or laboratory models at a stated preparation and dose.

EffectTarget tissuePlant partPreparationTest organismTest typeSource
HepatotoxicityLiverLive plantsSolvent extractionHorse (as animal)Case reportNo resolvable identifier
HepatotoxicityLiverAerial part of plantsDrying (dehydration)Horse (as animal)Short-term toxicityNo resolvable identifier
HepatotoxicityLiverLive plantsSolvent extractionHorse (as animal)Case reportNo resolvable identifier

Cited sources

The literature the compendium cites for this species. Metatron Health has no relationship with these authors or journals and earns nothing from citing them.

  1. van de Schans, M.G.M., Blokland, M.H., Zoontjes, P.W., Mulder, P.P.J., Nielen, M.W.F. Multiple heart-cutting two dimensional liquid chromatography quadrupole time-of-flight mass spectrometry of pyrrolizidine alkaloids. Journal of chromatography a, 2017, vol. 1503, p. 38-48. DOI
  2. Mudge, Elizabeth M., Jones, A. Maxwell P., Brown, Paula N. Quantification of pyrrolizidine alkaloids in North American plants and honey by LC-MS: single laboratory validation . Food additives and contaminants part a-chemistry analysis control exposure & risk assessment, 2015, vol. 32, no. 12, p. 2068-2074. DOI
  3. Stegelmeier, BL., Gardner, DR., James, LF., Molyneux, RJ. Pyrrole detection and the pathologic progression of Cynoglossum officinale (houndstongue) poisoning in horses . Journal of veterinary diagnostic investigation, 1996, vol. 8, no. 1, p. 81-90.
  4. KNIGHT, AP., KIMBERLING, CV., STERMITZ, FR., ROBY, MR. CYNOGLOSSUM-OFFICINALE (HOUNDS-TONGUE) - A CAUSE OF PYRROLIZIDINE ALKALOID POISONING IN HORSES . Journal of the american veterinary medical association, 1984, vol. 185, no. 6, p. 647-650.
  5. BAKER, DC., SMART, RA., RALPHS, M., MOLYNEUX, RJ. HOUNDS-TONGUE (CYNOGLOSSUM-OFFICINALE) POISONING IN A CALF. Journal of the american veterinary medical association, 1989, vol. 194, no. 7, p. 929-930.
  6. ElShazly, A., Sarg, T., Ateya, A., Aziz, EA., Witte, L., Wink, M. Pyrrolizidine alkaloids of Cynoglossum officinale and Cynoglossum amabile (family Boraginaceae) . Biochemical systematics and ecology, 1996, vol. 24, no. 5, p. 415-421. DOI
  7. PFISTER, JA., MOLYNEUX, RJ., BAKER, DC. PYRROLIZIDINE ALKALOID CONTENT OF HOUNDSTONGUE (CYNOGLOSSUM-OFFICINALE L) . Journal of range management, 1992, vol. 45, no. 3, p. 254-256. DOI

Boundary

A constituent measurement is a fact about material at a stated preparation, not a statement about what that material does in a person. An adverse-effect or genotoxicity record is an observation reported in a source, most often in an animal or laboratory model. Neither is a Metatron Health conclusion about causality, human risk or benefit, and the absence of a record is not proof that a preparation is safe. Nothing here is diagnosis, prescribing or individual medical care.

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