Cyathus stercoreus

The “dung-loving bird’s nest”, Cyathus stercoreus (Schwein.) de Toni. These specimens were found in Japan.

Synonyms

Cyathia stercorea (Schwein.) V.S. White
Bull. Torrey bot. Club 29: 266 (1902)

Nidularia stercorea Schwein.
Trans. Am. phil. Soc. 4(2): 253 (1832)

Common name

Dung loving bird’s nest

Description

Fruiting bodies: up to 1.5 cm tall x 4-8 mm wide, goblet-shaped (obconic) “nests”. The inner surface is nongrooved and nonfurrowed, which helps distinguish it from the related bird’s nest fungi Cyathus striatus. The outer surface is tomentose (more so when young) and yellow-brown in color, becoming smoother and darker in color in maturity. Periodioles are attached to the fruiting bodies by a thin cord called a funiculus. Peridioles are dark grey to black in color, 1-2 mm in diameter.
Spores: variable in size and shape, but typically globose or oval, smooth, thick-walled, and 18-40 x 18-30 µm. Further details about spore morphology may be found in Brodie and Dietrich (1977).
Habitat: this saprobic species is found growing on dung of herbivores, on soil containing manure, or on wood chips. Grows gregariously or in dense clusters.

The ultrastructure of this species has been described in detail (Flegler and Hooper, 1978).

Medicinal properties

Antioxidant effects

The polyketide antioxidative compounds, cyathusals A, B, and C as well as the previously known compound pulvinatal have been isolated from C. stercoreus (Kang et al., 2007). The cyathusals have antioxidant activity (measured by DPPH and ABTS radical scavenging assays) roughly comparable to reference antioxidants Trolox and BHA.

cyathusals-abc
Antioxidant polyketides from C. stercoreus: from left to right, cyathusals A, B, C.

Further investigations led to the discovery of of cyathuscavins A, B, and C along with the known compound 4-hydroxy-6-propenyl-pyran-2-one (Kang et al., 2008). The former 3 compounds showed good antioxidative activity, as measured by radical scavenging activity in the DPPH assay, and the ABTS+ assay. Cyathuscavins A and B (but not C) also scavenged superoxide (O2-) radicals more effectively than the control compound BHA. All three cyathuscavins also protected supercoiled DNA from Fenton reaction-mediated DNA breakage.

Cyathuscavin A.
Cyathuscavin A.
Cyathuscavin B.
Cyathuscavin C.
Cyathuscavin C.

4-hydroxy-6-propenyl-pyran-2-one.

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References

Brodie HJ, Dietrich HF.
Spore morphology in the Nidulariaceae fungi as revealed by the scanning electron microscope.
Can J Bot 1977 55(24):3042-3045.

Flegler SL, Hooper GR.
Ultrastructure of Cyathus stercoreus.
Mycologia 1978 70(6):1181-1190.

Kang H-S, Jun E-M, Park S-H, Heo S-J, Lee T-S, Yoo I-D, Kim J-P.
Cyathusals A, B, and C, antioxidants from the fermented mushroom Cyathus stercoreus.
J Nat Prod 2007 70(6):1043-1045.

Kang H-S, Kim K-R, Jun E-M, Park S-H, Lee T-S, Suh J-W, Kim J-P.
Cyathuscavins A, B, and C, new free radical scavengers with DNA protection activity from the Basidiomycete Cyathus stercoreus.
Bioorganic & Medicinal Chemistry Letters. 2008 18(14):4047-4050.

4 thoughts on “Cyathus stercoreus”

  1. How do you prevent and irradiate them? A mushroom killed my dog and I’m joe on a mission to remove all signs and opportunities for them to grow.

    Reply

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