USE OF KEFIR PEPTIDE FOR IMPROVING OR TREATING DEPRESSIVE BEHAVIORS AND RELATED DISEASES

Abstract

The invention discloses that a kefir peptide with an amino acid sequence of SEQ ID No: 2 or a fermentation product comprising the kefir peptide has an antidepressant activity, which means that by administering an effective amount of the kefir peptide or a composition comprising an effective amount of the kefir peptide to an individual with depressive behaviors is capable of effectively improving or alleviating the individual's depressive behaviors. Since the kefir peptide disclosed in the invention is not a chemical compound, the kefir peptide will not have side effects on the human body even taking it on a long-term basis.

Claims

1. A method for treating depression or suppressing depressive behaviors by administering an effective amount of a composition to an individual for enhancing an expression of BDNF (brain-derived neurotrophic factor) in hippocampal tissues of the individual and activating a BDNF/TrkB information channel, thereby improving or alleviating the individual's depressive behaviors or symptoms of depression; wherein: the composition comprises a kefir peptide, and an amino acid sequence of the kefir peptide comprises a sequence of SEQ ID No: 2.

2. The method as claimed in claim 1, wherein the amino acid sequence of the kefir peptide is SEQ ID No: 2.

3. The method as claimed in claim 1, wherein the composition further comprises a peptide with an amino acid sequence of SEQ ID No: 1.

4. The method as claimed in claim 1, wherein the composition further comprises another peptide with an amino acid sequence of SEQ ID No: 3.

5. The method as claimed in claim 2, wherein the composition further comprises another peptide with an amino acid sequence of SEQ ID No: 3.

6. The method as claimed in claim 3, wherein the composition further comprises another peptide with an amino acid sequence of SEQ ID No: 3.

7. The method as claimed in claim 1, wherein the composition is a BDNF (brain-derived neurotrophic factor) promoter.

8. The method as claimed in claim 1, wherein the composition is a kefir milk fermentation product.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0014] FIG. 1A is a chromatograph obtained after analyzing kefir fermentation product by HPLC.

[0015] FIG. 1B is a chromatograph obtained after analyzing peptide 1 isolated from kefir fermentation product by HPLC, wherein the retention time of peptide 1 is between 20 and 24 minutes.

[0016] FIG. 1C is a chromatograph obtained after analyzing peptide 2 isolated from kefir fermentation product by HPLC, wherein the retention time of peptide 1 is between 24 and 28 minutes.

[0017] FIG. 1D is a chromatograph obtained after analyzing peptide 3 isolated from kefir fermentation product by HPLC, wherein the retention time of peptide 1 is between 28 and 32 minutes.

[0018] FIG. 2A shows paths of a first group of mice observed by camera in an elevated plus maze test.

[0019] FIG. 2B shows paths of a second group of mice observed by camera in an elevated plus maze test.

[0020] FIG. 2C shows paths of a third group of mice observed by camera in an elevated plus maze test.

[0021] FIG. 2D shows paths of a fourth group of mice observed by camera in an elevated plus maze test.

[0022] FIG. 2E is the results of statistical analysis of the time it takes for the mice in each of the groups to enter all arm entrances of the elevated plus maze, wherein the “s” of Y axis represents second.

[0023] FIG. 2F is the results of statistical analysis of the time it takes for the mice in each of the groups to enter centers of the elevated plus maze, wherein the “s” of Y axis represents second.

[0024] FIG. 2G is the results of statistical analysis of the time it takes for the mice in each of the groups to enter open arms of the elevated plus maze, wherein the “s” of Y axis represents second.

[0025] FIG. 2H is the results of statistical analysis of the time it takes for the mice in each of the groups to enter closed arms of the elevated plus maze, wherein the “s” of Y axis represents second.

[0026] FIG. 3A shows movement paths of the first group of mice in an open field.

[0027] FIG. 3B shows movement paths of the second group of mice in an open field.

[0028] FIG. 3C shows movement paths of the third group of mice in an open field.

[0029] FIG. 3D shows movement paths of the fourth group of mice in an open field.

[0030] FIG. 3E is the results of statistical analysis of movement distance of the mice in each of the groups in an open field.

[0031] FIG. 3F is the results of statistical analysis of movement speed of the mice in each of the groups in an open field.

[0032] FIG. 3G is the results of statistical analysis of the time it takes for the mice in each of the groups to move to a center in an open field, wherein the “s” of Y axis represents second.

[0033] FIG. 3H is the results of statistical analysis of the time of the mice in each of the groups spent at a fixed position in an open field, wherein the “s” of Y axis represents second.

[0034] FIG. 4 is the results of statistical analysis of immobility and movement time of the mice in each of the groups in a swimming test.

[0035] FIG. 5 is the results of statistical analysis of immobility and movement time of the mice in each of the groups in a tail suspension test.

[0036] FIG. 6A is the expression results of BDNF (brain-derived neurotrophic factor) and CREB (cAMP responsive element-binding protein) mRNA in hippocampal tissues of the mice in each of the groups analyzed by quantitative RT-PCR.

[0037] FIG. 6B is the results of quantifying the BDNF mRNA expression levels in the hippocampal tissues of the mice in each of the groups.

[0038] FIG. 6C is the results of quantifying the CREB mRNA expression levels in the hippocampal tissues of the mice in each of the groups.

[0039] FIG. 6D is the results of BDNF and CREB protein expressions in the hippocampal tissues of the mice in each of the groups assessed by western blot analysis.

[0040] FIG. 6E is the results of quantifying BDNF protein expression levels in the hippocampal tissues of the mice in each of the groups.

[0041] FIG. 7A is the results of protein expression levels of p-TrkB (phosphorylated-TrkB)/TrkB protein in the hippocampal tissues of the mice in each of the groups assessed by western blot analysis.

[0042] FIG. 7B is the results of quantifying the expression levels of total TrkB protein in the hippocampal tissues of the mice in each of the groups.

[0043] FIG. 7C is the results of quantifying the expression levels of p-TrkB protein relative to total TrkB protein in the hippocampal tissues of the mice in each of the groups.

[0044] FIG. 7D is the results of protein expression levels of p-Erk1/2 (phosphorylated-ERK1/2)/Erk1/2 protein in the hippocampal tissues of the mice in each of the groups assessed by western blot analysis.

[0045] FIG. 7E is the results of quantifying the expression levels of total Erk1/2 protein in the hippocampal tissues of the mice in each of the groups.

[0046] FIG. 7F is the results of quantifying the expression levels of p-Erk1/2 protein relative to total Erk1/2 protein in the hippocampal tissues of the mice in each of the groups.

DETAILED DESCRIPTION OF THE INVENTION

[0047] The invention discloses that a kefir peptide or a fermentation product comprising the kefir peptide has an antidepressant activity, which means that by administering an effective amount of the kefir peptide or a composition comprising an effective amount of the kefir peptide to an individual with depressive behaviors is capable of effectively improving or alleviating the individual's depressive behaviors, and capable of enhancing an expression of BDNF (brain-derived neurotrophic factor) in the individual's hippocampal tissues and a capability of activating the BDNF/TrkB information channel. Therefore, the kefir peptide disclosed in the invention or the composition comprising an effective amount of the kefir peptide is capable of treating or improving depressive behaviors or diseases related to depressive behaviors, and can be developed into related compositions, such as functional foods, nutritional supplements, medicines. In addition, compared with the existing clinical drugs, since the kefir peptide disclosed in the invention is not a chemical compound, the kefir peptide will not have side effects on the human body even taking it on a long-term basis.

[0048] Further, when an individual is under pressure or other external factors that cause a reduction in an expression of BDNF in the hippocampal tissues, it will lead to the occurrence of depressive behaviors, and the examples disclosed in the invention prove that by administering the kefir peptide disclosed in the invention or the composition comprising the kefir peptide to an individual is capable of enhancing an expression level of BDNF in the hippocampal tissues and its downstream targets p-TrkB/TrkB, p-Erk1/2/Erk1/2, thereby achieving efficacies of improving the individual's depressive behaviors or diseases related to depressive behaviors.

[0049] The “kefir peptide” disclosed in the invention comprises an amino acid sequence of SEQ ID No. 2 or its amino acid sequence is SEQ ID No. 2, and the kefir peptide is prepared by artificial synthesis or a recombinant biological platform, or can be isolated from milk fermentation products.

[0050] For example, the kefir peptide disclosed in the invention can be isolated from a kefir fermentation product, wherein the kefir fermentation product is a mixture obtained by fermenting an animal milk, such as cow's milk with a kefir grain. The kefir fermentation product and the kefir peptide disclosed in the invention are analyzed with HPLC under the following conditions: the detection wavelength is 215 nm, the isolation column is a SEC column, the eluent is 100 mM phosphate buffer solution, 1M sodium chloride and 1 mM ethylenediaminetetraacetic acid (EDTA), pH 6.5, flow rate 0.5 ml/min, the results are shown in FIG. 1A and FIG. 1B, and by comparing the results in FIG. 1A with that in FIG. 1B, it can be known that the kefir fermentation product does comprise the kefir peptide disclosed in the invention.

[0051] Hereinafter, in order to verify the technical features and efficacies of the invention, a number of examples in conjunction with figures are illustrated for more detailed description as follows.

[0052] CD-1 mice used in the following examples are purchased from the National Laboratory Animal Center (NLAC), Taipei, Taiwan.

[0053] The peptide used in the following examples is isolated from kefir fermentation product, and can also be prepared by artificial synthesis.

[0054] The data in the following examples are presented in the form of average±standard deviation, and statistical analysis is performed by Duncan's test.

Example 1: Preparation of Peptide

[0055] After a milk is fermented and reacted by kefir grains, the kefir grains are removed and the fermented milk is lyophilized to obtain a kefir powder. According to calculations, the peptide content in the kefir powder is calculated as triglycine equivalent, 23.1 g/100 g.

[0056] Then, an isolation procedure is performed by HPLC, wherein the conditions used are mobile phase: 100 mM KH2PO4, 1 M NaCl, 1 mM EDTA (pH=6.5), flow rate 0.5 ml/min, detection at 215 nm; a molecular weight of the peptide is analyzed by LC-MS-MC, and the isolated peptide is confirmed and identified by using a library of known peptide sequences. The results are shown in FIG. 1A to FIG. 1D, and the amino acid sequences are shown in Table 1 below.

TABLE-US-00001 TABLE 1 The peptides and their sequences Serial number Amino acid in FIG. 1 Name Amino acid sequence sequence number 1 Peptide 1 TEIPAINTIASAEPTVH SEQ ID No: 1 3 Peptide 2 YQEPVLGPVRGPFPI SEQ ID No: 2 5 Peptide 3 KLHLPLPLVQSWM SEQ ID No: 3

[0057] In addition, the peptide 1, the peptide 2 or the peptide 3 can also be synthesized by chemical synthesis.

Example 2: Animal Test

[0058] Take 5-week-old CD-1 mice, provide standard laboratory animal feed (Altromin, Germany) and distilled water (dH2O), and keep them for 12 hours at 22-24° C. for light/dark cycles. Before starting the test, each group of mice are raised in an experimental animal room for 1 week to adapt to the environment, and then the mice are randomly divided into 4 groups, and the mice in each of the groups are treated and raised for 8 days (referred to as the first day of rearing to the eighth day of rearing) according to the following conditions:

[0059] the first group: take distilled water orally;

[0060] the second group: take 150 mg/kg milk powder orally;

[0061] the third group: take 150 mg/kg kefir fermentation product orally; and

[0062] the fourth group: take 10 mg/kg drug trazodone hydrochloride orally.

[0063] After the test, the mice in each of the groups are anesthetized and their hippocampal tissues are isolated, and frozen and preserved for use in subsequent examples.

Example 2: Elevated Plus Maze Test (EPMT)

[0064] The mice in each of the groups of Example 1 are treated for 6 hours according to the above conditions on the 7th day of rearing, and then an elevated plus maze test is performed, and paths of the mice in each of the groups within 5 minutes are observed with a camera. The results are shown in FIGS. 2A to 2D, and the time of the mice in each of the groups spent on open arms or closed arms in the elevated plus maze is analyzed, and the results are shown in FIG. 2E to FIG. 2H.

[0065] Comparing the results of FIG. 2A to FIG. 2D, it can be known that compared with the mice in the first group, the mice in the second group almost move to the open arms, the mice in the third group and the mice in the fourth group move to the open arms, and the paths of the mice in the third group in the open arms are more than that of the mice in the fourth group; also, from the results of FIG. 2F, it can be known that although the time it takes for the mice in the second to fourth groups to move to centers is longer than that of the mice in the first group, from the results of FIG. 2G and FIG. 2H, it can be known that compared with the mice in the second and fourth groups, the time of the mice in the third group on the open arms is significantly increased, and is shorter than the time on the closed arms. Therefore, the results from FIG. 2A to FIG. 2H show that by administering the composition comprising an effective amount of the kefir peptide of the invention to an individual is capable of effectively alleviating the individual's anxiety behaviors, and its effect of improving anxiety behaviors is better than that of antidepressant drugs used clinically.

Example 3: Open Field Test (OFT)

[0066] The mice in each of the groups in Example 2 are treated according to the above conditions for 30 minutes on the 8th day of rearing, and then an open field test is carried out. Specifically, the mice in each of the groups are first placed in an open field (45×45×40 cm) for 5 minutes, their travel paths and travel speeds are observed respectively, and the time it takes to reach the centers and the time spent at a fixed position are calculated. The results are shown in FIGS. 3A to 3H.

[0067] From the results of FIG. 3A to FIG. 3D, the behavior pattern of the mice in each of the groups in a new environment can be observed, and the third group of mice and the fourth group of mice are less anxious than the first group of mice; from the results of FIG. 3E to FIG. 3H, it can be known that compared with the first group of mice, the third and fourth groups of mice move a longer distance and move faster, and they are willing to spend time moving to the centers and spend less time at a certain fixed position without moving, indicating that the depressive behaviors of the third and fourth groups of mice have been improved.

[0068] From the results of this example, it can be known that the composition comprising an effective amount of the kefir peptide disclosed in the invention does have the capability to improve an individual's depressive behaviors, so the kefir peptide disclosed in the invention can be used as an active ingredient in antidepressant drugs or functional compositions.

Example 4: Forced Swimming Test (FST)

[0069] The mice in each of the groups of Example 2 are treated for 30 minutes according to the above conditions on the 7th day of rearing, and then a swimming test is carried out, testing time is 6 minutes. Movement and immobility time are measured and analyzed with a camera. The results are shown in FIG. 4, wherein the immobility time is a period of time without active movement but only floating in the water; the movement time is a period of time with active movement or circular movement.

[0070] From the results in FIG. 4, it can be known that the immobility and movement time of the first group of mice are 1.5±0.3 minutes and 2.5±0.3 minutes, respectively; the immobility and movement time of the third group of mice are 0.7±0.2 minutes and 3.3±0.3 minutes, respectively; the immobility and movement time of the fourth group of mice are 0.9±0.2 minutes and 3.1±0.3 minutes, respectively.

[0071] Comparison of the above results shows that compared with the first group of mice, the immobility time of the third and fourth groups of mice is significantly reduced (P<0.05), and the movement time is significantly increased (P<0.05); it can be known that by administering the composition comprising an effective amount of the kefir peptide disclosed in the invention to an individual with depressive behaviors is capable of improving the individual's depressive behaviors, and the improvement effect is close to that of antidepressant drugs used clinically.

Example 5: Tail Suspension Test (TST)

[0072] Refer to the steps of Example 2, the CD-1 mice are randomly divided into five groups and raised under the following conditions:

[0073] the first group: take distilled water orally;

[0074] the second group: take 150 mg/kg kefir fermentation product orally;

[0075] the third group: take the peptide 1 (10 mg/kg) disclosed in Example 1 orally, and the amino acid sequence is SEQ ID No: 1;

[0076] the fourth group: take the peptide 2 (10 mg/kg) disclosed in Example 1 orally, and the amino acid sequence is SEQ ID No: 2; and

[0077] the fifth group 5: take the peptide 3 (10 mg/kg) disclosed in Example 1 orally, and the amino acid sequence is SEQ ID No: 3.

[0078] When the mice in each of the groups are raised to the 7th day, after 30 minutes of treatment according to the following conditions, a tail suspension test is carried out for 6 minutes, and the immobility time is measured in the last 4 minutes. The results are shown in FIG. 5, wherein the immobility time refers to a period of time in which the mice are suspended and completely still.

[0079] From the results in FIG. 5, it can be known that the immobility and movement time of the first group of mice are 2.2±0.3 minutes and 1.8±0.3 minutes, respectively, while the immobility and movement time of the second, third, fourth, and fifth groups of mice are 2.0±0.3 minutes/2.0±0.3 minutes, 1.5±0.3 minutes/2.5±0.3 minutes, 1.0±0.2 minutes/3.0±0.2 minutes, and 1.8±0.3 minutes/2.2±0.3 minutes, respectively. The results in FIG. 5 show that compared with the first group of mice, the immobility time of the second group of mice administered with the kefir fermentation product is slightly reduced and the movement time is slightly increased, but comparing the data of the third group to the fifth group of mice, the immobility time (P<0.05) of only the fourth group of mice administered with the peptide 2 (i.e., the band 3 in FIG. 1A) is significantly reduced, and the movement time (P<0.05) of the mice is increased.

[0080] From the results of Examples 2 to 4, it can be clearly known that by administering the kefir fermentation product is capable of effectively improving the depressive behaviors and related diseases of a depressive individual, and the results of this example further confirm that the peptide 2 in the kefir fermentation product has an antidepressant activity, which means that by administering an effective amount of the peptide 2 (that is, the kefir peptide disclosed in the invention) is capable of achieving an efficacy of treating or preventing depressive behaviors and diseases related to depressive behaviors.

Example 6: Protein Expression Analysis

[0081] Expressions of protein and mRNA in the hippocampal tissues of the mice in each of the groups in Example 2 are assessed by quantitative RT-PCR method and western blot analysis, and the results are shown in FIG. 6 and FIG. 7, respectively.

[0082] From the results in FIG. 6A to FIG. 6C, it can be known that CREB (cAMP responsive element-binding protein) mRNA in the hippocampal tissues of the mice in each of the groups has not changed significantly, and compared with the first group of mice, expressions of BDNF mRNA in the third and fourth groups of mice can be significantly improved; further, from the results in FIG. 6D, it can be known that compared with the first group of mice, expression levels of BDNF protein in the hippocampal tissues of the third and fourth groups of mice are both increased by more than 2 times.

[0083] Furthermore, it can be known from the results of FIG. 7B and FIG. 7D that compared with the first group of mice, expression levels of TrkB and Erk1/2 protein in the hippocampal tissues of the third and fourth groups of mice have not change significantly, but it can be known from the results of FIG. 7C and FIG. 7E that a phosphorylation status of p-Erk1/2/Erk1/2 and p-TrkB/TrkB in the hippocampal tissues of the third and fourth groups of mice increases significantly (P<0.05).

[0084] The results of FIGS. 6 and 7 show that by administering the composition comprising the kefir peptide disclosed in the invention, such as the kefir fermentation product, is capable of effectively enhancing an expression level of BDNF protein in the hippocampal tissues of an individual, and enhancing an expression level of phosphorylation of p-Erk1/2/Erk1/2, and p-TrkB/TrkB, thus confirming that the kefir peptide disclosed in the invention or the composition comprising the kefir peptide disclosed in the invention is capable of effectively preventing or improving depressive behaviors and diseases related to depressive behaviors.

[0085] It is to be understood that the above description is only the embodiments and examples of the invention and is not used to limit the present invention, and changes in accordance with the concepts of the present invention may be made without departing from the spirit of the present invention. For example, the equivalent effects produced by various transformations, variations, modifications and applications made to the configurations or arrangements shall still fall within the scope covered by the appended claims of the present invention.