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Bioactivity Assessment of Veratrum californicum Alkaloids
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The native Idaho plant
Veratrum californicum
is known to contain steroidal alkaloids that function as
inhibitors of hedgehog signaling, a pathway utilized for the growth and differentiation of cells as well as proper tissue
development.
Veratrum californicum
was originally noticed when pregnant ewes consumed the plant and later gave
birth to lambs with craniofacial mutations such as a cyclopean eyes. These malformations were caused by the plant’s steroidal
alkaloid cyclopamine blocking the hedgehog signaling pathway. This same pathway is used by more than 20 types of cancer for
multiplication of cells. Additional alkaloids have been found in
Veratrum californicum
, which are being studied
in order to identify additional hedgehog signaling inhibitors. There are at least seven compounds detected in extracts that are
completely uncharacterized, twelve with proposed identities, and the six known alkaloids veratrosine, cycloposine, veratramine,
cyclopamine, isorubijervine, and muldamine all within
Veratrum californicum
. In this thesis these molecules were
extracted together from the root and rhizome of the plant, and then separated into five fractions using high performance liquid
chromatography. Mass spectrometry analysis identified the presence of twenty five alkaloids (nine more than literature precedent),
and software processing of the data predicted the molecular formulas for each known, suspected, and unknown alkaloid. The bioactivity
of the raw extract and each fraction was assessed by comparison to 0.1 μM cyclopamine, and it was found that three fractions
suppressed hedgehog signaling to a greater extent, indicating the presence of bioactive constituents worthy of further
investigation. Five fractions were collected at 2.5 min intervals, beginning at 10.25 min from time of raw extract injection.
Fraction 1 was most potent at Hh signal inhibition, and was determined to contain veratrosine, cycloposine, and an isomer of
each, followed by fractions 2 and 4, which possessed elevated bioactivity, but to a lesser extent than fraction 1. Fraction
2 was predicted to be comprised of cycloposine, its isomer, an isomer of veratrosine, tetrahydrojervine, veratramine, dihydrojervine,
its isomer, etioline, and five unknown compounds. Fraction 4 was composed of cyclopamine, and suspected to contain isomers of
veratramine and cyclopamine, isorubijervine, and muldamine, as well as two unknown alkaloids.
Title: Bioactivity Assessment of
Veratrum californicum
Alkaloids
Description:
The native Idaho plant
Veratrum californicum
is known to contain steroidal alkaloids that function as
inhibitors of hedgehog signaling, a pathway utilized for the growth and differentiation of cells as well as proper tissue
development.
Veratrum californicum
was originally noticed when pregnant ewes consumed the plant and later gave
birth to lambs with craniofacial mutations such as a cyclopean eyes.
These malformations were caused by the plant’s steroidal
alkaloid cyclopamine blocking the hedgehog signaling pathway.
This same pathway is used by more than 20 types of cancer for
multiplication of cells.
Additional alkaloids have been found in
Veratrum californicum
, which are being studied
in order to identify additional hedgehog signaling inhibitors.
There are at least seven compounds detected in extracts that are
completely uncharacterized, twelve with proposed identities, and the six known alkaloids veratrosine, cycloposine, veratramine,
cyclopamine, isorubijervine, and muldamine all within
Veratrum californicum
.
In this thesis these molecules were
extracted together from the root and rhizome of the plant, and then separated into five fractions using high performance liquid
chromatography.
Mass spectrometry analysis identified the presence of twenty five alkaloids (nine more than literature precedent),
and software processing of the data predicted the molecular formulas for each known, suspected, and unknown alkaloid.
The bioactivity
of the raw extract and each fraction was assessed by comparison to 0.
1 μM cyclopamine, and it was found that three fractions
suppressed hedgehog signaling to a greater extent, indicating the presence of bioactive constituents worthy of further
investigation.
Five fractions were collected at 2.
5 min intervals, beginning at 10.
25 min from time of raw extract injection.
Fraction 1 was most potent at Hh signal inhibition, and was determined to contain veratrosine, cycloposine, and an isomer of
each, followed by fractions 2 and 4, which possessed elevated bioactivity, but to a lesser extent than fraction 1.
Fraction
2 was predicted to be comprised of cycloposine, its isomer, an isomer of veratrosine, tetrahydrojervine, veratramine, dihydrojervine,
its isomer, etioline, and five unknown compounds.
Fraction 4 was composed of cyclopamine, and suspected to contain isomers of
veratramine and cyclopamine, isorubijervine, and muldamine, as well as two unknown alkaloids.
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