Milk and colostrum have high biological potential, and due to their natural origin and non-toxicity, they have many uses in cosmetics and dermatology. Research is ongoing on their potential application in other fields of medicine, but there are still few results; most of the published ones are included in this rentryview. These natural products are especially rich in proteins, such as casein, β-lactoglobulin, α-lactalbumin, lactoferrin, immunoglobulins, lactoperoxidase, lysozyme, and growth factors, and possess various antibacterial, antifungal, antiviral, anticancer, antioxidant, immunomodulatory properties, etc.
1. Introduction
Although milk is known to be used as a raw material in the food industry, it is also widely used in the pharmaceutical and cosmetic industries due to its considerable biological potential. It has also been the subject of detailed analyses and discussions of its individual components and their properties
[1][2][1,2].
Milk contains the nutrients required for the growth and development of the neonate. It contains a colloidal dispersion of specific proteins as micelles, fats organized in emulsified globules, as well as lactose, various minerals, and vitamins in solution
[3].
The composition of milk varies between species. The largest differences can be found between the protein content of individual species. Sheep milk and sheep colostrum is distinguished by the highest total protein and fat content, being almost one and a half that of cow or goat milk and colostrum ().
The initial milk, or colostrum, is produced by the mammary glands during pregnancy and immediately after delivery for about five days
[4][5][6][4,5,6]. Colostrum is yellow, has a slightly acidic pH of about 6.4, and a higher density than later milk. Due to its intended use, it has a much higher content of biologically active substances that affect the immune system of neonates.
Table 1. Composition of bovine, goat, and sheep colostrum and milk (%)
[3][7][8][9][10][11][12][13][3,7,8,9,10,11,12,13].
Component |
Colostrum |
Milk |
Bovine |
Goat |
Sheep |
Bovine |
Goat |
Sheep |
Lactose |
3.6 |
3.39–4.24 a |
3.3 |
4.6 |
4.1 |
4.8; 4.9 b |
Minerals |
0.9 |
0.85–0.9 a |
0.9 |
0.7 |
0.8 |
0.94; 1 b |
Proteins |
7.1 |
3.53–5.69 a |
11.8 |
3.4 |
2.9 |
5.5 |
Fats |
5.1 |
3.88–8.21 a |
13 |
3.7 |
4.5 |
6; 7.4 b |
Bovine colostrum is several times richer in caseins, β-lactoglobulins, α-lactalbumin, immunoglobulins, GMP (glycomacropeptide) lactoferrin, and growth factors than milk. For example, the immunoglobulins content ranges from 20 to 150 g/L in colostrum, but in the milk, only from 0.5 to 1.0 g/L. Only the content of lactoperoxidase and lysozyme remains at a similar level to both raw materials. Of all the types of colostrum presented, goat colostrum is the richest source of β-lactoglobulin. In goat colostrum, as in sheep colostrum, the content of β-lactoglobulin, α-lactalbumin, IgG, IgM, IgA, and lactoferrin is much higher than in milk of the same species. Sheep milk is rich in casein in comparison to goat and bovine milk; its content, equal to 4.6 g/L, is almost twice as high as in goat’s and cow’s milk (2.5 g/L and 2.7–2.8 g/L, respectively) (). Therefore, colostrum from each of the mentioned species could be used as a raw material supplying proteins, especially those with biologically active properties.
The main source of active molecules of milk consists of casein and whey proteins, which demonstrate a range of antimicrobial, antioxidant, and immunomodulatory properties, among others
[14]. Most biologically active proteins need to undergo proteolysis to achieve their full properties
[15][16][15,16]. Proteolysis naturally occurs in the digestive tract, but it can also be initiated by the enzymes naturally found in milk, as well as by coagulants or lactic acid bacteria, which are often used in the food industry
[15].
2. Bioactive Proteins of Milk
2.1. Casein
It belongs to the family of milk proteins containing phosphorus (phosphoprotein) and sugar (glycoprotein) residues; it consists of about 20 protein components. Caseins precipitate from raw, skimmed milk at a temperature of 20 °C at a pH of 4.6. The proteins of the four casein fractions (α
S1-, α
S2-, β-, and κ-casein) account for 80% of the total protein content in bovine milk. While 95% of the casein content is naturally self-assembled into casein micelles, i.e., spherical colloidal particles, approximately 10% is present in the form of single molecules as soluble casein. These two states,
viz. molecular and micellar casein, exist in equilibrium
[17]. Caseins can form dual-binding models that exploit their amphiphilic nature; interactions exist between hydrophobic regions of the proteins, with calcium phosphate clusters being linked to phosphoseryl clusters
[18].
2.1.1. Biological Properties of Casein
The phosphoproteins contained in casein regulate the calcium and phosphate metabolism in the body. Improvement in bone mineralization in experimental animals was observed in postmenopausal models
[19]. In addition, casein proteins inhibit tooth decay by increasing the calcium phosphate content in the plaque
[20] (). α-Casein, β-casein, αs1-casein, αs2-casein and κ-casein can transform into biologically active molecules. For example, α-casein forms an opioid, casomorphine, and α- and β-caseins are precursors of immunopeptides. In , the bioactive peptides that are released from casein and their properties are shown
[14][16][21][14,16,21].
Table 2. Major bioactive protein components of bovine, goat, sheep colostrum, and milk.
Proteins |
Colostrum |
Milk |
[Ref] |
Bovine |
Goat |
Sheep |
Bovine |
Goat |
Sheep |
Casein (g/L) |
2.6 |
n.d. |
n.d. |
* 2.7; 2.8 |
2.5 |
4.6 |
[14], * [22] |
κ-casein (%) |
n.d. |
n.d. |
n.d. |
* 12 |
** 20.4 |
* 9.1–10.2 a |
* [23][24], ** [22] |
αS1-casein (%) |
n.d. |
n.d. |
n.d. |
* 37 |
** 5.6 |
* 33.9–39.9 a |
* [23][24], ** [22] |
αS2-casein (%) |
n.d. |
n.d. |
n.d. |
* 10 |
** 19.2 |
* 12–16.4 a |
* [23][24], ** [22] |
β-casein (%) |
n.d. |
n.d. |
n.d. |
* 35 |
** 54.8 |
* 37–42.3 a |
* [23][24], ** [22] |
β-lactoglobulin (mg/mL) |
* 7.9–30 |
* 9.3–49.8 |
** 4–19 |
*** 3.3 |
**** 3.07 |
**** 5.97 |
* [25], ** [26], *** [14], **** [27] |
α-lactalbumin (mg/mL) |
* 3 |
** 2.77 |
*** 1.5–2 |
* 1.2 |
**** 1.27 |
**** 0.95 |
* [14],** [25],*** [26],**** [27] |
Immunoglobulins (g/L) |
20–150 |
n.d. |
n.d. |
0.5–1 |
n.d. |
n.d. |
[14] |
IgG |
* 15–180 |
** 50–60 |
*** 45–69 |
* 0.35; ** 0.59 b |
** 0.1–0.4 |
**** 0.35–1.62 |
* [28][29][30][31][32][33][34], ** [22], *** [35], **** [36] |
IgM |
* 4.2; ** 5 b |
* 1.6–5.2 |
*** 1.3–21.20 |
* 0.05 |
* 0.01–0.04 |
*** 0.2 |
* [13][37],** [28][29][30][31][32][33][34],*** [38] |
IgA |
* 3.5; **3.9 b |
** 0.9–2.4 |
*** 3.5 |
** 0.14 |
** 0.03–0.08 |
*** 0.2 |
* [28][29][30][31][32][33][34],** [13][37],*** [38] |
Glycomacro-peptide (g/L) |
2.5 |
n.d. |
n.d. |
1.2 |
n.d. |
n.d. |
[14] |
Lactoferrin (g/L) |
* 0.8; ***1.5–5 b |
** 0.38 |
** 0.74 |
* 0.02–0.2; 0.02–0.75 b |
* 0.098–0.15 |
* 0.14 |
* [39][40][41][42], ** [36], *** [43] |
Lactoperoxidase (g/L) |
* 0.02; *** 0.011–0.045 b |
** 0.062–0.204 |
n.d. |
* 0.03; *** 0.013–0.03 b |
n.d. |
n.d. |
* [14], ** [8], *** [6] |
Lysozyme (mg/L) |
* 0.14–0.7 |
n.d. |
n.d. |
** 0.37–0.6 |
** 0.25 |
** 1–4 |
* [ |
. It has been reported to have comparable cytotoxic activity against lung cancer, kidney, and bladder carcinoma cell lines
[44][87][88][44,87,88]. These findings suggest that such cytotoxic aggregates of apo-alpha-lactalbumin could be potential antitumor drugs.
2.3. β-Lactoglobulin
β-Lactoglobulin belongs to whey proteins and constitutes about 50% of these proteins
[89]. Its content in colostrum is much higher than in milk and amounts to 7.9–30 mg/mL
[6]. Structurally, it is a globular protein containing five cysteine residues, four of which are involved in the formation of disulfide bridges stabilizing the quaternary structure
[44]. β-Lg is a rich source of calcium ion binding peptides
[90].
Regarding its thermal stability, a temperature of 72 °C did not cause significant changes in the structure of the β-Lactoglobulin molecule in mixtures of other substances derived from milk; however, heating for 30 s at 100 °C resulted in significant changes, i.e., partial denaturation of particles
[91]. This globulin is a carrier of retinol and fatty acids and is known to bind vitamin D and stimulate lipase activity
[40][41][42][40,41,42]. In addition, when heated to 70–80 °C, it loses the ability to actively bind palmitic acid, vitamin D, and retinol
[92].
Biological Properties of β-Lactoglobulin
Hernandez-Ledesma et al. isolated several antioxidant peptides by hydrolysis with Corolase PP. Their antioxidant activity was slightly higher than that of butylated hydroxyanisole (BHA)
[93].
The β-Lg molecule also demonstrates significant antioxidant activity in milk, which, among others, has been attributed to the presence of sulfur-containing amino acids such as methionine
[89][90][91][89,90,91]. These amino acids are also believed to exert antitumor effects
[94]. Their activity is believed to be associated with the fact that methionine is a precursor of cysteine, which is needed for the formation of glutathione (GSH): a thiol antioxidant that scavenges reactive oxygen species, resulting in the formation of oxidized glutathione. Decreased amounts of GSH and a decreased GSH/GSSG ratio in tissues are biomarkers of oxidative stress. Chronic oxidative stress may lead to chronic inflammation and cancer development and progression
[95].
The protein demonstrates antimicrobial effects by inhibiting the adhesion of pathogens to surfaces and thus preventing their colonization
[80][96][80,96]. Bactericidal activity has been shown against both Gram-positive bacteria, such as
B. subtilis and
S. aureus, and Gram-negative ones, such as
E. coli and
Bordetella bronchiseptica [80]. Other studies also indicate that β-Lg chemically modified with 3-hydroxyphthalic anhydride, may be effective in inhibiting
Chlamydia trachomatis infection; in addition, 3-HP-β-lactoglobulin is active against herpes simplex virus HSV-1 and -2
[97].
2.4. Lactoferrin
One of the bioactive whey proteins is Lactoferrin (LF). It was first isolated in 1939 from cow milk and later from human milk in 1960
[98]. It demonstrates a similar iron-binding capacity to transferrin proteins
[44]. Lactoferrin is a monomeric glycoprotein; its polypeptide chain consists of two spherical lobes connected by a hinge region
[99].
It is resistant to high temperatures and proteolytic enzymes
[100]. LF can be found in saliva, bile, pancreatic fluid, amniotic fluid, and tears, but the highest concentration is found in human or porcine milk
[44]. It is a component of neutrophils, from which it is released into the bloodstream during trauma, infection, and inflammation
[101][102][103][101,102,103].
In milk, LF is mainly synthesized by glandular epithelial cells
[103]. Its concentration ranges from 20 to 200 mg/L in cow milk, 140 mg/L in sheep milk, and 98–150 mg/L in goat milk
[13][39][40][13,39,40]. Higher levels are found in the colostrum than in milk; for example, the level is around 0.8 g/L in cow colostrum
[41].
2.4.1. Biological Properties of Lactoferrin
Lactoferrin is a protein that is found in many body fluids such as colostrum, milk, tears, nasal secretions, saliva, and genital secretions. It is also produced in large quantities in neutrophils
[42]. Lactoferrin demonstrates bactericidal, bacteriostatic, antiviral, antifungal, antiparasitic, anticancer and antioxidant properties
[41][100][104][105][106][107][108][109][110][111][112][113][114][41,100,104,105,106,107,108,109,110,111,112,113,114]. In addition, several clinical studies have confirmed that bovine lactoferrin is an immune modulator that stimulates the phagocytic activity of multinucleated leukocytes
[107] and reduces the production of interleukin (IL)-6 and tumor necrosis factor (TNF)-α in cell cultures
[106]. The mechanisms of action of lactoferrin related to individual types of its activity were presented in .
Table 3. Mechanisms of lactoferrin action.
Kind of Activity |
Mechanism of Action |
[Ref.] |
Antibacterial |
- Reducing the concentration of iron ions that are necessary to bacterial growth and proliferation (chelation of iron via LF) - Interacting with lipoteichoic acid (LTA) of the cell walls of G(+) bacteria, disintegrating them and increasing their permeability |
[102][115][116] |
|
- Binding to lipopolysaccharide (LPS) of the walls of G(−) bacteria and disintegrating them. |
|
Antifungal |
- Damaging cell membranes of fungi and altering their permeability |
[117][118][119] |
- Sequestration of iron |
- Membrane destabilization |
Antiviral |
- Blocking the host’s cell surface receptors due to the LF’s affinity for glycosaminoglycans- Direct interacting with capsid or viral envelope proteins |
[113][120][121] |
Antiparasitic |
- Targets the host cell entry |
[122][123][124][125][126] |
|
- Sequestration of iron- Probably linked to sequestration of iron |
|
|
- Acts additively or synergistically with the antiparasitic compounds used in therapy |
|
Antioxidant |
- Inhibiting the propagation of hydroxyl radicals by sequestering cationic iron and copper |
[109][115][127] |
Anticancer |
- Reducing the production of tumor necrosis factor (TNF)-α in cell cultures |
[104] |
Immunomodulatory |
- Stimulating the phagocytic activity of multinucleated leukocytes |
[98][103][104] |
- Reducing the production of interleukin (IL) -6 in cell cultures |
- T-cell maturation |
- Stimulation of NK (natural killer cells) cells | 44 | ] | , ** | [ | 13 | ] |
Serum albumin (g/L) |
* 1.3 |
n.d. |
n.d. |
* 0.3 |
** 0.26–0.3 |
** 0.55–0.6 |
* [14], ** [45] |
Growth factors (µg/L) |
50 µg–40 mg/L |
n.d. |
n.d. |
<1 µg–2 mg/L |
n.d. |
n.d. |
[14] |
IGF-I |
* 0.049–2 a |
n.d. |
*** 0.199–0.265; ** 50–500 b |
* <0.002–0.101 |
**** 11–16.8 a |
** “low” |
* [46][47][48][49][50][51][52][53][54][55][56][57][58],** [59],*** [60],**** [61][62][63] |
IGF-II |
** 0.15–0.6 a |
n.d. |
n.d. |
** 0.002–0.1 a |
* 106 |
n.d. |
* [62], ** [46][51][56] |
EGF |
* 0.004–0.008; 0.3242 b |
n.d. |
** 1.7–2.3 |
<0.002; 0.155 b |
n.d. |
** <0.0008 |
* [64][65], ** [66] |
TGF-β1 |
0.0124–0.0426 |
n.d. |
n.d. |
0.0008–0.0035 |
n.d. |
n.d. |
[49] |
TGF-β2 |
0.15–1.15; 0.3 b |
n.d. |
n.d. |
0.013–0.07; 0.066 b |
n.d. |
n.d. |
[48][67] |