Pyrrolizidine alkaloids: analytical challenges and perspectives - - PowerPoint PPT Presentation

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Pyrrolizidine alkaloids: analytical challenges and perspectives

Professor Annie Bligh

BSc PhD CChem CSci FRSC FRSB FRSA

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Outline

Analytical challenges?

• What are pyrrolizidine alkaloids (PA)?
• Why are they toxic? How can the insects

manage the toxin?

• PA distribution in plants
• What are the analytical techniques

available?

Specificity and Sensitivity

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What are pyrrolizidine alkaloids (PAs)?

• PAs are plant defence weapons against

herbivores.

• They are present in several different plant species,

for example,

• Eupatorium (Asteraceae)
• Crotolaria (Fabaceae)
• Senecio (Asteraceae)
• PAs can occur in two forms, the tertiary free base

and the N-oxide.

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Some examples of Pas – free base

Retrorsine Heliotrine Echimidine Senecionine

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Common necine bases of PA

Retronecine N-oxide

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Why are they toxic?

• Genotoxic: Capable of forming DNA adduct
• Hepatotoxic: Veno-occlusive
• Damage to heart and lung in high dose
• The PA N-oxide itself, which is non-toxic per

se, cannot be directly converted into toxic pyrrols and is hydrophylic and unable to passively pass through membranes

• But N-oxide can be broken down to the free

base in the gut of insects and mammals, where it is absorbed and further reduced to highly unstable toxic pyrrols.

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• A. R. MATTOCKS

Toxicology Research Unit, MRC Laboratories, Surrey, UK

Toxicity of Pyrrolizidine Alkaloids

A new class of metabolite, with a pyrrole-like structure, has been demonstrated in the tissues of animals poisoned by pyrrolizidine alkaloids. There is some correlation between the degree of hepato-toxicity and the amount of "pyrrole" found in the liver. Evidence has been found of the types of reactions such metabolites might undergo with tissue constituents.

1968, vol 217, 723

Mattocks AR. Chemistry and toxicology of pyrrolizidine alkaloids. London: Academic Press, 1986.

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How can the insects manage the toxin?

• around 40 insect herbivores feed on the PA-

containing Senecio jacobaea

• insects are able to detoxify PAs in their host

plant through N-oxidation

• By N-oxidation potentially toxic free bases

are converted back into PA N-oxides that cannot be transformed into toxic pyrrolic derivatives

Attract and deter: a dual role for PAs in plant–insect interactions

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A: Larvae of the specialist moth Tyria jacobaeae feeding on their host plant Senecio jacobaea B: adult T. jacobaeae Both larvae and adults contain pyrrolizidine alkaloids and show warning coloring.

Photo: Eric Thomassen

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PAs distribution in plants

• In the roots, the PAs were almost

exclusively present as N-oxides and not as free bases.

• In the shoots around 35% of the PAs were

tertiary free bases.

• Younger leaves have higher PA

concentrations than the older leaves.

• For example, adonifoline in Senecio

scandens, flower > stem > root > leaf

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What are the analytical techniques available?

Separation

• thin layer chromatography (TLC)
• high performance liquid

chromatography (HPLC)

• UPLC
• gas chromatography (GC)
• supercritical fluid

chromatography (SFC) Detection

• colorimetry
• mass spectrometry (MS)
• nuclear magnetic

resonance (NMR)

• chemiluminescence (CE)
• Diode array detection

(DAD) However, most of these methods were strictly limited by the structural specificity of different types of PAs.

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Colorimetric

Not for OTO-PAs! Sensitivity: 5 ppm

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Pre-column derivatization HPLC-DAD

RET type of PAs Sensitivity 1 ppm

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UPLC-MS/MS - dual parent ion scans

• an effective strategy involving dual parent ion

scans of diagnostic ion pairs by UPLC-MS/MS

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Examples of PAs found in Senecio species. Senecionine N-

• xide is the basic

structure from which other PAs are formed. These senecionine type PAs have an

• tonecine

(senkirkine) or retronecine ester base (e.g., senecionine) and a 12-membered macro-cyclic ring

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PIS profile of PAs and main PAs in S. vulgaris

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UPLC-MS/MS - dual parent ion scans

• Two Senecio herbs, Sececio vulgaris L. and S.

scandens Buch.-Ham, showed great difference in their hepatotoxicity.

• Significant difference was shown between their

PAs’ fingerprint profiles.

• In all, 53 PAs, including 22 RET-PAs, 14 RET-PA-N-
• xides, 11 saturated-RET-PAs, 1 OTO-PAs, and 5

dehydro-OTO-PAs, were detected.

• The average content of PAs in S. vulgaris was

found about 25 times higher than that in S. scandens (1123.08 µg/g vs 44.31 µg/g)

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Conclusions

• What do we know about PAs ?
• Very toxic due to its reactivity to produce

dehydroPAs

• Structurally diverse

 Challenges in extraction  Challenges in specificity – impossible to have all the reference standards  Challenges in sensitivity

• Way forward?
• Better instrumentation
• Better database - algorithms

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Acknowledgements

Shanghai University of Traditional Chinese Medicine

• Professor Li Yang
• Professor Zhengtao Wang

Thank you