Biblio

Nom latin :chenopodium rubrum

Synonyme : Atriplex rubra

 

Nom français :chénopode rouge, patte d'oie rouge, ansérine rouge.

 

Nom anglais : red goosefoot

 

photo : http://home.worldonline.dk/garrido/chenopodium/rubrum.htm

 

- Hauteur: 15 à 100 cm.

- Tige dressée ou ascendante, souvent ramifiée dès la base.

- Feuilles un peu charnues, sans poils, non farineuses, ovales-triangulaires, profondément et irrégulièrement dentées, souvent teintées de rouge.

- Fleurs vertes ou rougeâtres en glomérules denses regroupés en panicule feuillée. 3-5 pétales de 1mm.

Fruit indéhiscent à 1 graine.

Source : http://www.dijon.inra.fr/malherbo/hyppa/hyppa-f/cheru_fh.htm

 

 

Localisation

Origine

 

Se trouve partout.

 

Propriétés

Utilisations

 

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photo : www.british-wild-flowers.co.uk/ G-Flowers/Goos...

 

 

L’infusion, d’une odeur peu agréable, aide à nettoyer le sang  et

à soigner les irritations de la peau.

On peut en boire en cas de constipation.

Source : http://membres.lycos.fr/maquillagefacil/arroche.htm

 

 

De même famille

Atriplex hortensis ex 'Rubra'

photo : www.secretseeds.com/ acatalog/Ap-Az.html.

 

Famille : Chenopodiaceae

Genre : Chenopodium

Autres espèces :

-c.vulvaria-voir dossier

-c.ambrosioides-voir dossier

-c.quinoa-voir dossier

-c.amaranticolor-voir dossier

-c.graveolens-voir dossier

-c.murale-voir dossier

-c.ficifolium-voir dossier

-c.botrys-voir dossier

-c.album-voir dossier

Références

[1-33]

 

 

1.       Mitrovic, A., et al., Changes in Chenopodium rubrum Seeds with Aging. Ann N Y Acad Sci, 2005. 1048: p. 505-8.

2.       Veit, J., E. Wagner, and J.T. Albrechtova, Isolation of a FLORICAULA/LEAFY putative orthologue from Chenopodium rubrum and its expression during photoperiodic flower induction. Plant Physiol Biochem, 2004. 42(7-8): p. 573-8.

3.       Ehness, R., et al., Glucose and Stress Independently Regulate Source and Sink Metabolism and Defense Mechanisms via Signal Transduction Pathways Involving Protein Phosphorylation. Plant Cell, 1997. 9(10): p. 1825-1841.

4.       Scanlon, C.H., et al., Identification and Preliminary Characterization of a Ca2+- Dependent High-Affinity Binding Site for Inositol-1,4,5-Trisphosphate from Chenopodium rubrum. Plant Physiol, 1996. 110(3): p. 867-874.

5.       Machackova, I., et al., Diurnal Fluctuations in Ethylene Formation in Chenopodium rubrum. Plant Physiol, 1997. 113(3): p. 981-985.

6.       Schwenger-Erger, C., W. Barz, and N. Weber, Fatty acid alteration of plastidic and extra-plastidic membrane lipids in metribuzin-resistant photoautotrophic Chenopodium rubrum cells as compared to wild-type cells. Z Naturforsch [C], 2001. 56(11-12): p. 1047-56.

7.       Martinec, J., et al., Subcellular localization of a high affinity binding site for D-myo-inositol 1,4,5-trisphosphate from Chenopodium rubrum. Plant Physiol, 2000. 124(1): p. 475-83.

8.       Walczysko, P., E. Wagner, and J.T. Albrechtova, Use of co-loaded Fluo-3 and Fura Red fluorescent indicators for studying the cytosolic Ca(2+)concentrations distribution in living plant tissue. Cell Calcium, 2000. 28(1): p. 23-32.

9.       Lozhnikova, V., E. Komarova, and G. Muromtsev, Ultrastructure of Chenopodium rubrum L. apices during the effect of fusicoccin and photoperiodic induction. Cell Biol Int, 2000. 24(6): p. 399-403.

10.     Kolar, J., C.H. Johnson, and I. Machackova, Presence and possible role of melatonin in a short-day flowering plant, Chenopodium rubrum. Adv Exp Med Biol, 1999. 460: p. 391-3.

11.     Peters, W., et al., Growth, ageing and death of a photoautotrophic plant cell culture. Planta, 2000. 210(3): p. 478-87.

12.     Goetz, M. and T. Roitsch, The different pH optima and substrate specificities of extracellular and vacuolar invertases from plants are determined by a single amino-acid substitution. Plant J, 1999. 20(6): p. 707-11.

13.     Schwenger-Erger, C., N. Bohnisch, and W. Barz, A new psbA mutation yielding an amino-acid exchange at the lumen-exposed site of the D1 protein. Z Naturforsch [C], 1999. 54(11): p. 909-14.

14.     Banzet, N., et al., Accumulation of small heat shock proteins, including mitochondrial HSP22, induced by oxidative stress and adaptive response in tomato cells. Plant J, 1998. 13(4): p. 519-27.

15.     Greiner, S., S. Krausgrill, and T. Rausch, Cloning of a tobacco apoplasmic invertase inhibitor. Proof of function of the recombinant protein and expression analysis during plant development. Plant Physiol, 1998. 116(2): p. 733-42.

16.     Ehness, R. and T. Roitsch, Co-ordinated induction of mRNAs for extracellular invertase and a glucose transporter in Chenopodium rubrum by cytokinins. Plant J, 1997. 11(3): p. 539-48.

17.     Debel, K., et al., The 23-kDa light-stress-regulated heat-shock protein of chenopodium rubrum L. is located in the mitochondria. Planta, 1997. 201(3): p. 326-33.

18.     Obermeyer, G., A. Sommer, and F.W. Bentrup, Potassium and voltage dependence of the inorganic pyrophosphatase of intact vacuoles from Chenopodium rubrum. Biochim Biophys Acta, 1996. 1284(2): p. 203-12.

19.     Schlattner, U., et al., Binding of adenylate kinase to RNA. Biochem Biophys Res Commun, 1995. 217(2): p. 509-14.

20.     Scanlon, C.H., et al., Characterisation of inositol 1,4,5-trisphosphate receptors from Chenopodium rubrum. Biochem Soc Trans, 1995. 23(4): p. 574S.

21.     Roitsch, T., M. Bittner, and D.E. Godt, Induction of apoplastic invertase of Chenopodium rubrum by D-glucose and a glucose analog and tissue-specific expression suggest a role in sink-source regulation. Plant Physiol, 1995. 108(1): p. 285-94.

22.     Reifarth, F.W., T. Weiser, and F.W. Bentrup, Voltage- and Ca(2+)-dependence of the K+ channel in the vacuolar membrane of Chenopodium rubrum L. suspension cells. Biochim Biophys Acta, 1994. 1192(1): p. 79-87.

23.     Roitsch, T. and W. Tanner, Expression of a sugar-transporter gene family in a photoautotrophic suspension culture of Chenopodium rubrum L. Planta, 1994. 193(3): p. 365-71.

24.     Weiser, T. and F.W. Bentrup, Pharmacology of the SV channel in the vacuolar membrane of Chenopodium rubrum suspension cells. J Membr Biol, 1993. 136(1): p. 43-54.

25.     Schwenger-Erger, C., et al., Metribuzin resistance in photoautotrophic Chenopodium rubrum cell cultures. Characterization of double and triple mutations in the psbA gene. FEBS Lett, 1993. 329(1-2): p. 43-6.

26.     Kishore, N., A.K. Mishra, and J.P. Chansouria, Fungitoxicity of essential oils against dermatophytes. Mycoses, 1993. 36(5-6): p. 211-5.

27.     Knack, G., Z. Liu, and K. Kloppstech, Low molecular mass heat-shock proteins of a light-resistant photoautotrophic cell culture. Eur J Cell Biol, 1992. 59(1): p. 166-75.

28.     Specht, U. and G. Richter, Expression of early genes in light-induced chloroplast differentiation of cultured plant cells. J Photochem Photobiol B, 1991. 11(2): p. 173-87.

29.     Weiser, T. and F.W. Bentrup, Charybdotoxin blocks cation-channels in the vacuolar membrane of suspension cells of Chenopodium rubrum L. Biochim Biophys Acta, 1991. 1066(1): p. 109-10.

30.     Weiser, T. and F.W. Bentrup, (+)-Tubocurarine is a potent inhibitor of cation channels in the vacuolar membrane of Chenopodium rubrum L. FEBS Lett, 1990. 277(1-2): p. 220-2.

31.     Heeger, V., K.W. Leienbach, and W. Barz, [Metabolism of nicotinic acid in plant cell suspension cultures, III: Formation and metabolism of trigonelline (author's transl)]. Hoppe Seylers Z Physiol Chem, 1976. 357(8): p. 1081-7.

32.     Brenner, W. and W. Engelmann, Heavy water slows down the photoperiodic timing of flower induction in Chenopodium rubrum. Z Naturforsch [C], 1973. 28(5): p. 356.

33.     Teltscherova, L. and H. Havlickova, Reversal of the inhibitory effect of (2-chloroethyl)trimethyl-ammonium chloride on the flowering of Chenopodium rubrum L. by kinetin. Experientia, 1967. 23(10): p. 861.