COMPOSITIONS CONTAINING A PEPTIDE ABLE TO STIMULATE THE GPRC6A-DEPENDENT SIGNALING PATHWAY

Abstract

Disclosed are pharmaceutical or nutraceutical compositions comprising the peptide having the sequence NMYLPPVPPP PVVPTF or extracts containing it, in admixture with suitable excipients.

Claims

1. Pharmaceutical or nutraceutical compositions comprising a peptide having sequence NMYLPPVPPPPVVPTF (SEQ ID NO:1) in isolated form or isolated proteins containing said sequence or extracts containing said sequences or isolated proteins.

2. Compositions according to claim 1 wherein the peptide is contained in extracts of Phaseolus vulgaris.

3. Compositions according to claim 1 further comprising additional active ingredients having complementary or synergic activity.

4. Method of treating conditions benefiting from stimulation of the GPRC6A-dependent signalling pathway with the compositions according to claim 1 in patients in need thereof, said method comprising administering said compositions to said patient.

5. The method according to claim 4 wherein the conditions comprise male hypogonadism, osteopenia/osteoporosis, erectile dysfunction and metabolic syndrome.

Description

DESCRIPTION OF THE INVENTION

[0005] It has now been discovered that an amino-acid sequence exhibits close homology (62.5% amino-acid identity; 75% structural similarity) with domain 141-161 of SHBG (SHBG.sub.141-161), corresponding to a protein loop with high flexibility responsible for the interaction between ucOCN and GPRC6A.

[0006] It has also been found that said peptide sequence (NMYLPPVPPPPVVPTF, SEQ ID 1, P80762) stimulates insulin and testosterone release in experimental models of cell line cultures.

[0007] The object of the invention is therefore pharmaceutical or nutraceutical compositions comprising the peptide having the sequence NMYLPPVPPP PVVPTF in isolated form or isolated proteins containing said sequence or extracts containing said sequences or isolated proteins, in admixture with suitable excipients.

[0008] The compositions according to the invention are useful in the treatment of conditions that benefit from stimulation of the GPRC6A-dependent signalling pathway. Examples of such conditions include male hypogonadism, osteopenia/osteoporosis, erectile dysfunction and metabolic syndrome.

[0009] As well as the peptide having the sequence indicated, the invention also comprises the use of peptides that exhibit at least 75%, preferably at least 80%, and more preferably at least 90% homology, compared with sequence P80762 (SEQ ID 1). For example, peptides wherein sequence NMYLPPVPPPPVVPTF has been modified with conservative substitutions of amino acids and/or deletions of 1-4 amino acids can be used according to the invention.

[0010] The peptide NMYLPPVPPPPVVPTF and its homologues can be prepared by conventional peptide synthesis methods. Alternatively, a natural source containing said peptides, in particular Phaseolus vulgaris extracts containing the protein fraction of said species, can be used.

[0011] The extracts can be obtained from varieties of Phaseolus vulgaris subjected to suitable enzymatic hydrolysis processes followed by extraction with aqueous or alcohol-based solvents.

[0012] The compositions according to the invention can be administered orally, transdermally or parenterally.

[0013] Examples of suitable forms of administration include capsules, tablets, solutions, suspensions, gels, transdermal patches and the like. The peptides contained in the Phaseolus extract can be combined with other ingredients having complementary or otherwise useful activity such as vitamins, amino acids and antioxidants, minerals such as zinc and magnesium salts, and phytotherapeutic extracts (such as Panax ginseng, Ginkgo biloba, green tea, Vitis vinifera, Vaccinium myrtillus, Serenoa repens, Aloe vera, Cynara scolymus, Citrus aurantium and Zingiber officinalis).

[0014] The effective doses of the peptides will be determined by the skilled person on the basis of pre-clinical and clinical tests. The doses will depend on various factors, such as the type and severity of the patient's disorder or condition, and the patient's weight, sex and age. However, an average daily dose could range from 10 to 1000 mg of peptide, or the equivalent of the extract containing it.

[0015] The efficacy of the formulations according to the invention can be deduced from in vitro studies conducted on INS-1 rat insulinoma and MA-10 mouse Leydig cell tumour cell lines, using kidney bean flour of commercial origin. The results, reported in the experimental section below, demonstrated the release of insulin (FIG. 2) and testosterone (FIGS. 1 and 3). Expression of GPRC6A was confirmed in both cell lines [Brar Diabetes. 2017; De Toni Endocrinology. 2014].

[0016] The following examples illustrate the invention in greater detail.

Example 1 Testosterone Release from MA-10 Mouse Leydig-Cell Tumour Cell Cultures

[0017] MA-10 mouse Leydig-cell tumour cells, cultured to 90% confluence in 24-well multiwell plates, were stimulated with different agonists for 12 hours at 37° C. under sterile conditions, according to an already validated protocol [Cormier Cell Biol Toxicol. 2018]. The control (CTRL) contained no agonists. The results relate to testosterone release, expressed as ng of testosterone (T) per μg of total protein, obtained from cell extract. The histograms show the effect on testosterone release of uncarboxylated osteocalcin (OCN, 3 ng/mL) and peptide SEQ ID 1 (Peptide, 10.sup.−6M). Significance: *=P<0.05 vs. CTRL.

Example 2 Insulin Release from INS-1 Murine Insulinoma Cell Cultures

[0018] INS-1 rat insulinoma cells, cultured to 90% confluence in 24-well multiwell plates, were stimulated with different combinations of secretagogue agonists for 2 hours at 37° C. under sterile conditions, according to an already validated protocol [Hohmeier Diabetes. 2000]. The results relate to insulin release, expressed as the normalised variation in low-concentration glucose (Gluc 3 mM) at the baseline control. Stimulation with the phosphodiesterase inhibitor IBMX (Gluc 1 mM+IBMX) represents the maximum secretagogue stimulation and positive control of the experiment. The four histograms in FIG. 2a show the effect on insulin release of arginine (Arg, at concentrations ranging from 2.5 to 20 mM), a known GPRC6A agonist, while the release of three Phaseolus extracts (Ph1400179, Ph31721 and Ph32046, at concentrations ranging from 0.0005 to 5 mg/mL), is shown in FIGS. 2b-d respectively. Significance: *, ** and ***=P<0.05, 0.01 and 0.001 respectively vs the baseline control.

Example 3 Testosterone Release from MA-10 Mouse Leydig-Cell Tumour Cell Cultures

[0019] MA-10 mouse Leydig-cell tumour cells, cultured to 90% confluence in 24-well multiwell plates, were stimulated with different agonists for 12 hours at 37° C. under sterile conditions, according to an already validated protocol [Cormier Cell Biol Toxicol. 2018]. The control (CTRL) contained no agonists The results relate to testosterone release, expressed as normalised variation vs the CTRL. The four histograms in FIG. 3a show the effect on testosterone release of arginine (Arg, at concentrations ranging from 2.5 to 20 mM), a known GPRC6A agonist, while the release of three Phaseolus extracts (Ph1400179, Ph31721 and Ph32046, at concentrations ranging from 0.0005 to 5 mg/mL), is shown in FIGS. 3b-d respectively. Significance: *, ** and ***=P<0.05, 0.01 and 0.001 respectively vs the baseline control.

REFERENCES

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