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Ugly Duckling or a Swan:
Ricin
Is it truly ugly?
or
a swan waiting to be discovered!
Preamble
• Ricin: Extensively researched since 1888, and first protein
responsible for the beginning of Immunology.
• For more than a century notoriously known as ‘Good for
Nothing’.
• Recently published (February 2017) research paper at
‘Matters’ debunks the ‘sheer nuisance’ theory around
Ricin.
• Though known to be dermally inactive, Ricin induced hair
follicle dystrophy, not just in lab animals but also in human
hair follicles in culture.
• The scientific findings of this study present a possibility of
creating a new treatment for unwanted hair, an unmet in
need in cosmetic industry.
Pilot studies
• The action of ricin and related
protein abrin was examined on
hair follicle (HF) and re-growth
of hair.
• Topical application of ricin
after hair is removed by
waxing, resulted in ‘sparse’
and ‘delayed re-growth’ of
hair.
• Histopathological examination
of untreated (C) HFs show
normal ladder-like pattern (as
indicated by arrowheads) and
ricin treated HFs show
dystrophy in H-E stained
mouse skin.
In vivo studies
• Ricin treated hair follicles
showed immediate dystrophic
catagen induction and were
found to be dystrophic.
• The characteristic features of
ricin treated hair follicles
resembled chemotherapy
induced hair follicle dystrophy
such as
• Presence of many ectopic
melanin granules,
• Follicular and hair shaft
distortion and
• Irregular diameter of hair
bulbs
Human HF organ culture
• In vitro human hair
follicle organ culture, of
ricin and abrin treated
hair follicles showed;
– inhibition of hair shaft
elongation,
– premature HF
regression,
– hair follicle dystrophy.
Untreated hair follicle
Ricin-treated hair follicles
Toxicological studies
• Acute oral toxicity test :
– Ricin (200 μgm/ml) solution was found to be safe at 2000 mg/kg.
– No clinical signs of intoxication were observed
– no mortality observed.
• Acute dermal toxicity test : The Sub acute (14 days) dermal toxicity with ricin (200
μgm/ml) showed
– No mortality at a dose of 2000 mg/kg body weight. All the
– Animals appeared normal and showed no clinical signs of intoxication.
– No change in the food consumption was observed.
• Sub acute dermal toxicity test : The Sub acute (90 days) dermal toxicity studies with
ricin (200 μgm/ml) found to have
– No mortality at a dose of 1000 mg/kg body weight. All the
– Animals appeared normal and showed no clinical signs of intoxication.
– No change in the food consumption was observed.
– No statistically significant difference in the haematology and blood chemistry parameters
• The histopathology of liver, kidney and heart did not show any toxicity
• Ricin was found to be safe for sub-acute dermal test for 90 days for a dose
equivalent to human dose of 160μg/kg dose each.
Where are we now?
Observations propose ricin to be a promising
topical candidate for inhibiting growth of hair
follicle by inducing dystrophy without
adversely affecting other skin structures.
• Paper: https://sciencematters.io/articles/201702000001

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Ricin: Ugly Duckling To Swan

  • 1. Ugly Duckling or a Swan: Ricin Is it truly ugly? or a swan waiting to be discovered!
  • 2. Preamble • Ricin: Extensively researched since 1888, and first protein responsible for the beginning of Immunology. • For more than a century notoriously known as ‘Good for Nothing’. • Recently published (February 2017) research paper at ‘Matters’ debunks the ‘sheer nuisance’ theory around Ricin. • Though known to be dermally inactive, Ricin induced hair follicle dystrophy, not just in lab animals but also in human hair follicles in culture. • The scientific findings of this study present a possibility of creating a new treatment for unwanted hair, an unmet in need in cosmetic industry.
  • 3. Pilot studies • The action of ricin and related protein abrin was examined on hair follicle (HF) and re-growth of hair. • Topical application of ricin after hair is removed by waxing, resulted in ‘sparse’ and ‘delayed re-growth’ of hair. • Histopathological examination of untreated (C) HFs show normal ladder-like pattern (as indicated by arrowheads) and ricin treated HFs show dystrophy in H-E stained mouse skin.
  • 4. In vivo studies • Ricin treated hair follicles showed immediate dystrophic catagen induction and were found to be dystrophic. • The characteristic features of ricin treated hair follicles resembled chemotherapy induced hair follicle dystrophy such as • Presence of many ectopic melanin granules, • Follicular and hair shaft distortion and • Irregular diameter of hair bulbs
  • 5. Human HF organ culture • In vitro human hair follicle organ culture, of ricin and abrin treated hair follicles showed; – inhibition of hair shaft elongation, – premature HF regression, – hair follicle dystrophy. Untreated hair follicle Ricin-treated hair follicles
  • 6. Toxicological studies • Acute oral toxicity test : – Ricin (200 μgm/ml) solution was found to be safe at 2000 mg/kg. – No clinical signs of intoxication were observed – no mortality observed. • Acute dermal toxicity test : The Sub acute (14 days) dermal toxicity with ricin (200 μgm/ml) showed – No mortality at a dose of 2000 mg/kg body weight. All the – Animals appeared normal and showed no clinical signs of intoxication. – No change in the food consumption was observed. • Sub acute dermal toxicity test : The Sub acute (90 days) dermal toxicity studies with ricin (200 μgm/ml) found to have – No mortality at a dose of 1000 mg/kg body weight. All the – Animals appeared normal and showed no clinical signs of intoxication. – No change in the food consumption was observed. – No statistically significant difference in the haematology and blood chemistry parameters • The histopathology of liver, kidney and heart did not show any toxicity • Ricin was found to be safe for sub-acute dermal test for 90 days for a dose equivalent to human dose of 160μg/kg dose each.
  • 7. Where are we now? Observations propose ricin to be a promising topical candidate for inhibiting growth of hair follicle by inducing dystrophy without adversely affecting other skin structures. • Paper: https://sciencematters.io/articles/201702000001