Wuttke, Wolfgang (Bovenden, DE)
Jarry, Hubertus (Neu-Eichenberg, DE)
Christoffel, Volker (Buchberg, DE)
Spengler, Barbara (Neumarkt, DE)

Plaque It! Sponsored by: Flash of Genius

10/490190

08/19/2008

09/16/2002

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Bionorica AG (Neumarkt, DE)

424/725

A61K36/00

5382430	Method for the stimulation of the immune system of an animal by use of limulus test-positive plant glycolipid	January, 1995	Soma et al.
5411733	Antiviral agent containing crude drug	May, 1995	Hozumi et al.
5569459	Pharmaceutical compositions for the management of premenstrual syndrome and alleviation of menopausal disorders	October, 1996	Shlyankevich
5716646	Methods and compositions for treating arthritis	February, 1998	Smith et al.
5795574	Use of an extract from a non-photosynthetic filamentous bacterium and composition containing it	August, 1998	Breton et al.
5916565	Product and method for treating joint disorders in vertebrates	June, 1999	Rose et al.	424/756
5952374	Method for inhibiting the development of Alzheimer's disease and related dementias- and for preserving cognitive function	September, 1999	Clarkson, Jr. et al.
6008208	Compositions and methods for treating bone deficit conditions	December, 1999	Petrie et al.
6242012	Herbal composition for promoting hormonal balance in women and methods of using same	June, 2001	Newmark et al.
6267994	Use of extract of cimicifuga racemosa	July, 2001	Nesselhut
6326366	Hormone replacement therapy	December, 2001	Potter et al.
6471997	Iridaceae extract and compositions containing it	October, 2002	Breton et al.
20010025059	Composition and method for treating non-bacterial prostatitis	September, 2001	Kastke	516/70
20020010141	Isoflavones for treatment of obesity	January, 2002	Ingram
20020172732	Composition comprising cocoa	November, 2002	Ter Laak et al.

CN1090498	August, 1994
CN1158261	September, 1997
CN1159340	September, 1997
CN11158261	September, 1997
DE361762	June, 1992
EP0847755	November, 1997			Use of an extract of cimicifuga racemosa
HU204197	December, 1991
JP63030417	February, 1988			ANTI-ALLERGIC AGENT
JP07138179	May, 1995			CELL ACTIVATOR CONTAINING EXTRACT FROM BELAMCANDA CHINENSIS DC. AND ITS APPLICATION
JP07138181	May, 1995			INHIBITOR OF TESTOSTERONE 5ALPHA-REDUCTASE CONTAINING EXTRACT FROM BELAMCANDA CHINENSIS DC. AND ITS APPLICATION
JP09030977	February, 1997			THERAPEUTIC AGENT FOR BONE DISEASE CONTAINING EXTRACT OF BLACK COHOSH ROOT
JP09124499	May, 1997
JP090301884	November, 1997
JP10007580	January, 1998			COLLAGENASE INHIBITOR
JP10084923	April, 1998			FERMENTED BEVERAGE OF SCARLET FLAG-LEAVED WATSONIA BULB EXTRACTION LIQUID AND ITS PRODUCTION
WO/1997/009056	March, 1997			EXTRACT OF IRIDACEAE AND COMPOSITIONS CONTAINING SUCH EXTRACT
WO/1997/015398	May, 1997			METHOD FOR PRODUCING A LIME PRODUCT FROM MUSSEL- AND/OR SEASHELLS
WO/1999/047419	September, 1999			ROBUST SINGULARITY AVOIDANCE IN SATELLITE ATTITUDE CONTROL
WO/2001/074345	October, 2001			ISOFLAVONES FOR TREATMENT OF OBESITY
WO/2002/036140	May, 2002			USE OF A PREPARATION OF CIMICIFUGA RACEMOSA
WO/2002/007321	September, 2002			DIGITAL SIGNAL ENCODING APPARATUS AND METHOD, DIGITAL SIGNAL DECODING APPARATUS AND METHOD, AND DIGITAL SIGNAL TRANSMISSION SYSTEM

Gura; Science (1997), vol. 278, pp. 1041-1042.
Milewicz, A., et al, “Vitex agnus castus-Extrakt zur Behandlung von Regeltempoanomalien infolge latenter Hyperprolaktinamie,” Arzneimittel Forsch 43: 752-756 (1993 (in German).
Hoberg, E., et al., “Diterpenoids from the Fruits of Vitex agnus-castus,” Phytochemistry 52: 1555-1558 (1999).
Gorkow, “Klinischer Denntnisstand von Agni-casti fructus,” Z. Phytotherapie 20: 159-168 (in German), 1999.
Einer-Jensen, N., et al., “Cimicifuga and Melbrosia Lack Oestrogenic Effects in Mice and Rats,” Maturitas 25: 149-153 (1996).
Rote Liste 1986 (Editio Cantor, Aulendorf, Wurttemburg).
Esaki, S., “Pharmacological Studies of Tectoridin and Tectorigenin,” Nippon Yakurigaku Zasshi 64: 186-198 (1968).
Petersen, F.J., Materia Medica and Clinical Therapeutics, “Cimicifuga racemosa,” 1905.
Li, J.X., et al, “Effects of Cimicifugae Rhizoma on Serum Calcium and Phosphate Levels in Low Calcium Dietary Rat . . . ,” Phytomedicine 3:379-385 (1996/97).
Duker, E.-M., et al., “Die Wirking von Extrakten aus Cimicifuga racemosaauf die Gonadotropinfreizetzung in Menopausalen Frauen und . . . ”, Planta Med. 57:420-424 (1991).
Sorrentino, L. and Genazzanai. E., “Vascular Action of Acteina: Active Constituent of Actaea raemosaL.,” Nature 12:544-545 (1962).
Kumar, T., and Shawl, A.S., “Isoflavonoids from Iris crocea,” Phytochemistry 31: 1399-1401 (1992).
Lin, M. and Zhou, L.X., “Studies on Chemical Constituents of Belamcanda chinensis (L.) DC (II),” Chin. Chem. Lett. 8:133-134 (1997).
Wooten, G., “The Herbal Database,” 1984, www.okanoganl.com/natural/chem/hrbdata.htm.
List, P.H. and Horhammer, L., eds., An Hagers Handbuch der Pharmazeutischen Praxis (4th ed., Springer-Verlag, Berlin, 1972), vol. 3 pp. 375-376 (in German).
Jarry, H., et al., “Treatment of Menopausal Symptoms with Extracts of Cimicifuga racemosa: In viv . . . ,” Phytopharmaka Forsch. Klin, Anwend 99-122 (1995).
Homoopathisches Arzneibuch 2000 (Deutscher Apotheker Verlag Stuttgart), entitled “Iris versicolor,”.
F. Borrelli & E. Ernst, “Cimicifuga recemosa: A systematic review of its climical efficacy,” Eur.J.Clin.Pharmacol. 58: 235-241.
J. Liu, et al., “Evaluation of Estrogenic Activity of Plant Estracts for the Potential Treatment of Menopausal Sumptoms,” J.Agric.FoodChem. 49: 2472(2001).
C. Willis, “Herb to Know—Black Cohosh—Cimicifuga racemosa,” at http://www.wisetouch.com/blackcohosh.html, published May 22, 2002.
Montemuro, Dr. Suzanne, “Alternatives to H.R.T. and the Menopausal Woman,” The Soc. of Obstetricians and Gynaecologists of Canada, 1996, Publ. May 22, 2002.
Kawase, A., et al., “Flavonoid of Iridacea. II. Chemical Structure of ao New Isoflavone Glucoside, Homotectoridin, Isolated Together with Tectoridin from the Rhizomes of Iris germanica,” Agric. & Biol. Chem. (1973), pp. 145-150, V. 37 (abstract).
Pailer, M. & Franke, F., “Constitutes of Iris germanics,” Monatsh. Chem., (1973), pp. 1394-1408, V. 104 (abstract).
Li, Y., et al., “Flavonoids of Iris dichotoma Pall,” Yaoxue Xuebao, (1986), pp. 836-841, V. 21 (abstract).
Lu, Y., et al., “Quantitative Analysis for the Three Main Isoflavonoids in the Chinese Drug, Shegan, by TLC/HPLC-Densitometry,” Yaowu Fenxi Zazhi, (1987), pp. 275-279 V. 7, abstract.
Huang, M., “Studies on the TLC and Assay of Belamcanda chinensis (L.) DC, Iris tectorum Maxim and Iris dichotoma Pall,” Yaowu Fenxi Zazhi, (1997), pp. 112-115, V. 17 (abstrac.
Eskai, S., et al., “Physiological Studies on Tectoridin and Tectorigenin,” Nippon Yakurigaku Zasshi, (1968), pp. 186-198, V. 64 (in Japanese), entire article.
Web page: “Garden Web's Hortiplex Plant Database”, at: http://hortiplex2.gardenweb.com/plants/p1/gw1020997/html—accessed Dec. 19, 2004.
Web page: “Iris pallida illyrica”, at: http://www.zaplana.net/flowers/asp/display—flower [Zaplana.net]—accessed Dec. 16, 2004.
Diel, P. et al., “Ability of xeno- and pythoestrogens to odulate expression of estrogen-sensitive genes in rat uterus . . . ,” J. Steroid Biochem.Mol.Biol. 73:1-10 (2000).
Whitten, P. & H.B. Patisaul, “Cross-species and interassy comparisons of phythoestrogen action,” Environ.Health Perspect. 109s1: 5-20 (2001).
Blaschek, W. et al., eds., “Drogen A-K”, Folgeband 2 (Springer-Verlag, Berlin, 1998), pp. 374-378 (in German).
Pschyrembel, “Wörterbuch Naturheilkunde und alternative Heilverfahren” (Walter de Gruyter, Berlin, 1996), p. 52 (in German).
Ezaki, S., “Pharmacological Effects of Tectoridin and Tectorigenin,” J. Japan Pharmacol. Assoc. (1968), 64:186-198.
S. Ezaki, “Pharmacological Studies of Tectoridin and Tectorigenin,” Nippon Yakurigaku Zasshi 64: 186-198 (1968) (original publication in Japanese), Chemical Abstracts, v. 69, p. 9822, Abstract No. 104972j.
J.X. Li et al., “Anti-Osteoporotic Activity of Traditional Medicines—Active Constituents of Cimicifugae Rhizome,” J. Tradit. Med. 12:816-817 (1995).
H. Jarry & G. Harnischfeger, “Studies on the Endocrine Effects of the Contents of Cimicifuga racemosa 1. Influence on the Serum Concentration of Pituitary Hormones in Ovariectomized Rats,” Planta Medica 1:46-49 (1985).
H. Jarry et al., “Studies on the Endocrine Effects of the Contents of Cimicifuga racemosa2: In Vitro Binding of Compounds to Estrogen Receptor,” Planta Medica 4:316-319 (1985).
E.-M. Duker et al., “Effects of Extracts of Cimicifuga racemosaon Gonadotropin Release in Menopausal Women and Ovariectomized Rats,” Planta Med. 57:420-424 (1991).
Revilla et al., “Comparison of Several Procedures Used for the Extraction of Anthocynains from Red Grapes,” J. Agric. Chem. 46:4592-4597 (1998).
Phillipson, “New Drugs from Nature—It Could Be Yew,” Phytotherapy Research 13:2-8 (1999).
Pereira et al., “Plant and Plant-Derived Compounds Employed in Prevention of Osteoporosis,” Acta. Farm. Bonaerense 21(3):223-34 (2002).
Ososki et al., “Phytoestrogens: A Review of the Present State of Research,” Phyto. Res. 174:845-869 (2003).

Hoffman, Susan C.

Catalyst Law Group, APC
Farber, Michael B.

The invention claimed is:

1. A method for alleviating a prostatic disorder selected from the group consisting of benign and malignant prostate hyperplasy comprising the step of administering an estrogen-type organoselective medicament to alleviate the prostatic disorder, the medicament comprising an extract from a Cimicifuga species.

2. The method of claim 1 wherein the Cimicifuga species is selected from the group consisting of: C. racemosa, C. foetida, C. dahurica, C. heracleifolia, C. simplex, C. japonica, C. europaea, C. acerina, C. elata, C. rubifolia.

3. The method of claim 2 wherein the Cimicifuga species is C. racemosa.

4. The method of claim 1 wherein the extract is produced from a Cimicifuga species by extraction with an organic solvent, such that the method alleviates the prostatic disorder.

5. The method of claim 1 wherein the extract is produced from a Cimicifuga species by extraction with a mixture of an organic solvent and water, such that the method alleviates the prostatic disorder.

6. The method of claim 1 wherein the extract is produced from a Cimicifuga species by extraction with supercritical CO₂, such that the method alleviates the prostatic disorder.

The present invention relates to a use of extracts from Cimicifuga species.

It is known from WO99/47 149 (=EP1064009A1) to the applicant of the present application that extracts from Cimicifuga racemosa have an estrogenic effect not on the uterus, however in the hypothalamo-hypophysary axis, in the cardiovascular system, and in the bone. Insofar extracts from Cimicifuga racemosa have been utilized in order to produce an estrogen-type, organoselective medicament having no uterotrophic effect.

17β-estradiol, which is formed in women's ovaries (any mention of estradiol hereinbelow refers to physiological 17β-estradiol) [hereinafter also referred to as E ₂ ], has a generally proliferation-enhancing effect in the organism. In addition to controlling the female cycle, it i. a. also has a homeostatic effect on the functions of urethra, bladder, and vagina. In men, locally formed estradiol as well as the male sexual hormone testosterone also have a proliferation-enhancing effect in the bladder and in the prostate.

During menopause, lowering of the estradiol level takes place due to cessation of the ovarial function. This results in weakening of proliferative processes in many organs, with subsequently occurring degeneration and reduced functional capacity.

With lack of estrogen, cystitis frequently develops in the post-menopausal woman as a consequence of reduced mucous membrane in the urethra and thus facilitated ascension of germs.

Urinary incontinence frequently occurring post-menopausally is equally caused by lack of estrogen. These disorders may be prevented or alleviated, respectively, by timely administration of estradiol.

Hormonal regulation of the function of the bladder in men presumably is similar to that in women; in any case the hitherto known regulative principles in the urinary bladder of male and female rats are very similar.

The administration of estrogens having a nonselective proliferative action is particularly adverse for uterus and breast tissue, for uncontrolled growth may occur here owing to the insufficiency or lack of gestagen counter-regulation.

Up to the present, there is no medicament available from plant drugs that might be used for an organoselective prophylaxis or therapy of changes in the uro-genital tract in the event of estrogen deficiency.

Starting out from this prior art, it accordingly is an object of the present invention to furnish plant medicaments having a sexual hormone-type action while having an organoselective action with no effect or only little effect on the uterus.

This object is achieved through the use of extracts from Cimicifuga species, particularly Cimicifuga racemosa.

In particular, the present invention relates to

• • use of extracts from Cimicifuga species, particularly Cimicifuga racemosa , for producing an estrogen-type organoselective medicament having no uterotrophic effect or one that is at least negligible, wherein
  • the medicament is used for alleviating sexual hormone-related disorders of the uro-genital tract.
  • Use is preferred in the following, post-menopausally occurring disorders: cystitis and dry vagina.
  • Moreover the present invention relates to a use of extracts from Cimicifuga species, particularly Cimicifuga racemosa , for producing an estrogen-type organoselective medicament having no uterotrophic effect or one that is at least negligible, wherein
  • the medicament is utilized for alleviating benign and malignant prostate hyperplasy.

It was surprisingly found that Cimicifuga racemosa extract, for example from the rhizoma of Cimicifuga racemosa , also has effects similar to those of estradiol in the urinary bladder and in the urethra of ovarectomized rats. In the bladder both the estrogen receptor ER-alpha and ER-beta are expressed. It was found that estradiol and Cimicifuga analogously regulate down the gene expression of the estrogen receptor-alpha in the urinary bladder. Thus it appears that besides innervation, the bladder tonus may also be influenced through steroid hormones.

FIG. 1 shows a diagram which represents the differential bladder tonus of ovarectomized rats (group sizes: 12 animals). Following a three-month treatment of ovarectomized rats with Cimicifuga racemosa extract, the maximum pressure in the urinary bladder [in mm Hg] and the minimum pressure [in mm Hg] following relaxation of the bladder were determined by instillation of 1 ml of physiological saline solution.

The diagram in accordance with FIG. 1 shows on the ordinate the differential pressure [in mm Hg] between maximum and minimum pressure, which is an indication for the elasticity of the urinary bladder.

In comparison with placebo controls following a treatment with Cimicifuga extract, a significant dosage-dependent increase of bladder elasticity, measured through the pressure difference between relaxed and definedly filled bladder, is found.

In the test system, estradiol is found to be the most effective substance.

The highest Cimicifuga dose (400 mg/kg/d) triggers an effect comparable to that of the synthetic SERM (Selective Estrogen Receptor Modulator), Raloxifen.

Thus an additional effect of the extract on the urinary bladder, namely, an improvement of bladder incontinence, is equally proven.

Benign prostate hyperplasy and prostate carcinoma in men may also be influenced favorably by inhibition of the local estrogen production, but also by inhibiting synthesis of the male sexual hormones.

The like active mechanisms may also be demonstrated on the male castrated rat for the Cimicifuga racemosa extract. In the course of trials by the inventors of the present application, it was found that estradiol and the Cimicifuga extract significantly inhibit gene expression of the estrogen receptor of the alpha-subtype in the prostate without having an effect on the gene expression of the estrogen receptor-beta.

Both in in-vivo experiments in the rat prostate in the whole-body model and in human prostate carcinoma cells it was surprisingly found that Cimicifuga racemosa extracts have an anti-androgenic action favorably influencing prostate carcinoma and significantly inhibiting growth of the tumor cells in vitro.

In the prostate of castrated male rats, gene expression of the proliferation-enhancing growth factor IGF1 is moreover regulated up by testosterone, however regulated down by Cimicifuga , as is desired for reducing the hyperplasy. The prostate regression induced by castration could be antagonized in the rat by testosterone. In analogy with the findings in the case of castrated rats not treated with androgen (see above), the IGF1 expression regulated up by testosterone (see above) could also be regulated down by the Cimicifuga extract. These findings clearly demonstrate that the testosterone-induced prostate growth may be inhibited by extracts from Cimicifuga species.

In experiments on the human prostate-Ca line LNCAP, 5 alpha-dihydrotestosterone-induced proliferation and the production of its prostate-specific antigen (PSA) may significantly be inhibited by Cimicifuga species, particularly Cimicifuga racemosa.

Inasmuch as IGF1 always participates in the proliferation not only of benign but also malignant tumors, the inhibitory effect of extracts from Cimicifuga species on IGF1-gene expression in conjunction with this finding is evidence for an inhibitory effect on the prostate carcinoma.

As regards manufacture of the extract in accordance with the invention, WO99/47 149 is herewith fully included herein by reference, the essential features of which are, however, presently summarized as follows:

It was found through in-vitro and in-vivo experimentation that extracts produced both from Cimicifuga species, particularly Cimicifuga racemosa , with organic solvents or mixtures of organic solvents with water or with supercritical CO ₂ have an organoselective effect on the uro-genital system, with an effect on the uterus being absent.

Thus the extracts used in accordance with the invention are suited for producing a ready-formulated medicament for the selective treatment and/or prophylaxis of sexual hormone-related disorders of the uro-genital tract.

Furthermore they are suitable for producing a ready-formulated medicament for the selective treatment and/or prophylaxis of post-menopausal urinary bladder infections.

They are moreover suited for producing a ready-formulated medicament for the treatment of benign and malignant prostate hyperplasies.

It was moreover found that enriched and/or pure ingredients or groups of ingredients from Cimicifuga species essentially have the same effects as the whole extract.

Ingredients or groups of ingredients to be particularly taken into consideration are the following: triterpenes, e.g., acteol and cimicigenol derivatives; polyphenols, such as caffeic acid and its derivatives, chlorogenic acid, piscidic acid, fucinolic acid, ferulic and isoferulic acid, cimicifugic acids; formononetine; alkaloids, e.g. cytisine and methylcytisine.

These ingredients are, besides in Cimicifuga racemosa , also found in additional Cimicifuga species such as, e.g., C. foetida, C. dahurica, C. heracleifolia, C. simplex, C. japonica, C. europaea, C. acerina, C. elata, C. rubifolia.

These further Cimicifuga species may thus also be used for producing extracts, and thus medicaments against the sexual hormone-related disorders of the uro-genital tract that are being mentioned in the context of the present invention.

Preferably rhizoma, roots, stalks, leaves and/or petals of the plants are used for producing the extracts.