The collagen enhancement by Spirulina extract in intrinsic and extrinsic skin aging in albino rat

doi:10.21203/rs.3.rs-2481209/v2

The aging of the skin is considered a cumulative process that is classed as intrinsic or extrinsic. Environmental factors like sun exposure and air pollution are considered the main cause of extrinsic aging. Mainly, intrinsic aging reflects the genetic background and depends on time. Spirulina platensis unicellular blue-green algae have a variety of biological and nutritional activities because of their high level of nutrients. The current study aims to investigate the mechanism by which spirulina extract (SE) may act anti-aging in female albino rats. Animals were received SE only, UV radiation only and both. In addition, two intrinsic groups as control old and old rats received SE. Spirulina extract (20mg/mL) was injected subcutaneously before UVA irradiation (2.16 J/cm2), daily for 7 days. The epidermal thickness and the collagen fibers layer were stained utilizing Hematoxylin and Eosin and Masson. There were improvements in the activities of antioxidants including superoxide dismutase (SOD) and reduced glutathione (GSH), downregulating in expressions of inflammatory cytokines; Interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α). As well as the recovery of collagen density, and reducing the production of matrix metalloproteinases were presented. The results found that spirulina extract may delay the signs of skin aging by enhancing collagen.

Biological sciences/Biological techniques

Biological sciences/Cell biology

Biological sciences/Drug discovery

Biological sciences/Immunology

Biological sciences/Physiology

Health sciences/Health occupations

collagen

skin aging

Oxidation

Spirulina

Algae

Skin is the largest organ in the body and acts as the first line of defense between the body's internal organs and the outside world. The skin acts as an immune organ to detect infections preventing infringements of pathogens, ultraviolet radiation (UVR), and mechanical, thermal and physical injury [1, 2]. Therefore, caring for the skin is imperative to better health and not a luxury. There are two types of skin aging, intrinsic and extrinsic [3]. Intrinsic aging is known as chronological aging and is defined as the natural aging process depending on normal biological processes. The intrinsic aging is influenced by the internal factors that include changes in gene expression, changes in the neuroendocrine system, and development of skin disorders disrupting the cutaneous barrier functions or skin involvement in connective tissue disorders [4]. Extrinsic aging, also known as photo-aging, on the other hand, is a phenomenon that can be somewhat resisted. Our skin ages prematurely as a result of numerous extrinsic, or external, factors that frequently cooperate with natural aging. Exposure to (UVR) is the most detrimental factor for this reason [5]. UVA radiation (400-320 nm) is about 95-98% of the total UV rays that reach the surface of the earth, as well as penetrate deeper than UVB (290–320 nm), into the skin, inducing alterations of the dermal connective tissue. Therefore, UVA is considered the main culprit responsible for skin cancers and photoaging [6]. Yogianti et al. [7] revealed that the intense exposure to UV radiation is a risk factor for the development of skin cancers. Photoaged skin appears very dry, has coarse wrinkles, and has telangiectasia and pigmentations, while, intrinsic chronological aging is smooth, pale, dry, and has fine wrinkles. In general skin aging appears as many atrophy-related symptoms, such as epidermal thinning and irregular collagen and elastic fibers [8]. It is commonly acknowledged that the primary cause of intrinsic and extrinsic aging is the destruction of the antioxidant defense systems (SOD, CAT, GSH) and the accumulation of damage of reactive oxygen species (ROS) [8]. In addition, the disturbed defense mechanism include antioxidant molecules such as vitamins A, C, and E., are leading to accumulation of damage of reactive oxygen species (ROS) [9]. Excess ROS activates extracellular matrix (ECM) remodeling proteins including matrix metalloproteinases (MMPs) such as MMP-1, MMP-3, and MMP-9. MMP-1 mainly initiates directly collagen breakdown; that are considered one of the most important factors affect skin aging [10, 11]. There is a great demand for natural products to delay the effects of skin aging [12, 13]. Spirulina (Arthrospira platensis) is unicellular blue-green algae that belongs to the cyanobacteria group. Spirulina strongly induces antioxidant enzyme activity, helps to prevent lipid peroxidation and DNA damage, and scavenges free radicals [14]. Spirulina also exerts a variety of immunomodulatory and anti-inflammatory activities by regulating key cytokines, including interleukin (IL)-1β, IL-2, IL-4, IL-6, IL-10, and tumor necrosis factor (TNF)-α [14]. There are many components in Spirulina including, several minerals, proteins, essential fatty acids, polysaccharides, pigments, including β-carotene, vitamins, antioxidants, a large number of peptides, amino acids, and immunologically effective compounds [15‒17]. These components make Spirulina extract (SE) a potential pharmaceutical for cosmetic product developments and basically for skin disease resistance. The target of this study is to assess the influence of intrinsic and extrinsic factors on aging and their resistance by Spirulina extract.

Algal extract

Spirulina algal extract was purchased from (Aim Grow Biotech Co., Ltd, China) as a dark green powder that contains 67.97% dry weight proteins, β-Carotene (120 mg/100 g), 6% lipids and 10.5% phycocyanin.

Skin Photoaging Model and Treatment:

UVA lamp (F15T8/BL, Hitachi, Japan) 15W was used for UV irradiation. To achieve a UVA spectral radiance of 300 μW/cm2. The distance between the lamp and the rats was 20 cm. The dorsal hair of all rats was removed with a shaver within an area of 2.5 -3 cm2 and exposed to radiation daily for 2hs/day in one session for a week, with daily dose of 2.16 J/cm². Animals of irradiated groups were taken the doses equally as one group. A UV radiometer (TM 208, Tenmars, Taiwan) was used to measure the lamp's radiation output as described by [18].

Treatment

Spirulina extract (SE) was weighed and dissolved in 9% normal saline. A total of 200 μL of extract and vehicle (saline) were injected subcutaneously into the shaved dorsal skin for respective treatment groups at a daily dose of (20 mg/mL), SE was injected one hour before irradiation.

The animals and the design of the experiment

A number of 42 (Rattus norvegicus) female albino rats were used in the present study divided by age into 28 young females (6-8 weeks old) weighing 120-180 g and 14 old females (20 -22 months old) weighing 250-300 g. The animals of the study were obtained from the National Center for Radiation Research and Technology, Cairo, Egypt, and confirmed by Benha University committee for animal care with ethical approval: ZD/FSc/BU-IACUC/2022-13. Animals were adapted for 1 week and were kept in metal cages in a well-ventilated space. All experiments were performed in accordance with relevant named guidelines and regulations. The authors complied with the ARRIVE guidelines. Rats were allotted into 6 groups (7 animals each) as follows:

The extrinsic experiment

Group I (GI): control young rats were (only subjected to shaving).

Group II (GII): young rats received SE (20 mg/mL) daily for a week.

Group III (GIII): young rats were administered a daily dose of saline and an hour later exposed to UVR (2.16 J/cm2), daily for a week.

Group IV (GIV): young rats received SE (20 mg/ml) and an hour later exposed to UVR (2.16 J/cm2), daily for a week.

The intrinsic experiment

Group V (GV): control old rats were (only subjected to shaving), considering (GI) as a young control.

Group VI (GVI): old rats received SE (20 mg/ml) daily for a week.

Histopathological study

Forty-eight hours after the last irradiation, animals of each group were decapitated under anesthesia of

xylazine 7 mg/kg and Ketamine 100mg/kg (Alfasan, Woerden-Holland, Holland). Samples of hairless skin were obtained from the rats' backs, which were then sliced into quarter-inch strips and soaked in 10% buffered formalin for routine histology study. Slices were pigmented with Hematoxylin and Eosin stain (H&E) to investigate the thickness of the epidermis, and Masson's trichrome stain to investigate the collagen fibers' density. Masson's trichrome staining of rat skin tissue. Collagen is stained blue-green, while cytoplasm, red blood cells, and nuclei are stained red. Stained images were investigated and captured using a light microscope (Bio-med, Japan) with a digital camera (RAS-312, LAINSY Co., Egypt). The observations of skin slides were done by Omer Ghoneimy, Associate Prof of Histology, Benha University and revised by Seham Ahmed, Professor of Histology, Benha University

Homogenization:

Skin tissue samples were homogenized in phosphate buffer saline (PBS) as previously described method [19] using Laboratory Homogenizer (GLH 850, Omni International, USA).

Immunological study

The level of reactive oxygen species (ROS) was evaluated in the homogenate skin colorimetrically using a colorimetric kit (Biodiagnostic Company, Giza, Egypt) according to a previously described method [20]. The activities of superoxide dismutase (SOD) were measured according to a previously described method [21], using Bio-diagnostic kits (Giza, Egypt). Reduced glutathione (GSH) was measured as a previously described method [22], using Bio-diagnostic kits (Giza, Egypt). Interleukin-1β (IL-1β) and tumor necrosis factor-α (TNF-α) were evaluated using enzyme‐linked immunosorbent assay (ELISA) kits (Elabscience Company, USA) following the manufacturer's protocol using a multi-mode microplate reader (BMG Labtec, Manchester, UK) at 450 nm.

Physiological study (Collagen biosynthesis)

The activity of Hydroxyproline (Hyp) levels was evaluated in skin homogenate according to a previously described method [23], while skin matrix metalloproteinase-1 (MMP-1) was measured using a commercial ELISA kit (Elabscience Company, USA) following the manufacturer's protocol.

Statistical analysis

The values of measured and studied parameters were expressed by the mean of 7 individual values (M) ± standard deviation (SD) and correlation analysis to assess the strength of association between two variables by using the SPSS (version 25) program produced by IBM Software, Inc. (Chicago, USA). One-way analysis of variance (ANOVA) was used for statistical analysis, followed by Duncan's test as a post hoc test [24]. A p-value was considered significant if p <0.05.

Histopathological study

Hairless Rat morphology

Skin backs of control and Spirulina extract-treated groups appeared relaxed, no wrinkles or inflammation (Fig. 1A, 1B). UVA-irradiated rats showed distinct features: dark-brown color, deep wrinkle, and acutely inflamed surface (Fig. 1C). After treatment the UVA-irradiated group was treated with SE, the appearance of the skin was greatly improved as relaxed surface with mild wrinkles, recovered inflammation and wound healing (Fig. 1D). The skin of the old rats showed irregular epidermal thickening with fine wrinkles (Fig. 1E). The old-aged rats treated with SE had a greatly improved skin when compared with control rats (Fig. 1A, 1F)

Epidermal thickness

Hematoxylin and eosin (H&E) staining showed increased epidermal thickness (hyperplasia) and the formation of deep wrinkles in the UVA-irradiated group (GIII) compared with control (GI) (Fig. 2A). Irradiated rats also, showed atrophy of the sebaceous gland and thickening of the wall of blood vessels. While SE-administrated group (GIV) showed abundant photoprotective activity and retained an intact epidermal layer of the skin (Fig. 2A). On the other hand, decreased atrophy of the epidermis and relative improvement in skin wrinkle formation of the old treated group (GVI) was observed compared with control old rats (GV), which showed remarkable wrinkle formation, epidermal thickening and desquamation compared with control young (GI) (Fig. 2B).

Dermal Collagen Fiber

Using Masson’s trichrome stain, the effect of SE administration on dermal collagen fibers in the dorsal skin was assessed. In the control group (GI), collagen fibers with blue dye were abundantly found in the dermis of the dorsal skin (Fig. 3A). However, in the UVA group (GIII), collagen was apparently destructed with follicular atrophy (Fig. 3A). In contrast, UVA with SE received group (GIV), showed amelioration of the reduced collagen fibers compared to the UVA group (pale color). There was manifested clear inflammatory infiltration and hemorrhage in the whole dermis in the UVA group (GIII) compared with the other groups, however the UVA + SE received group (GIV) showed a noticeable recovery (Fig. 3A). The intrinsic aging showed no great change of collagen layer in old groups, except little destruction in the group (GV) compared to the young control group (GI) (Fig. 3B).

Immunological study

When compared to both the control group (GI) and the UVA+ SE treated group (GIV), the levels of ROS in the UVA group (GIII) significantly increased, as indicated in (Table 1, Fig. 4). Additionally, the levels of ROS in SE-treated old rats (GVI) were significantly decreased compared with the control old rats (GV) (p < 0.05), and eventually returned to the levels of control young rats (GI). Additionally, compared with the control group and UVA+ SE received group (GIV) the UVA irradiation group (GIII) showed a significant decline in SOD activities and GSH levels (p < 0.05). The same results were shown in the old control rats (GV) when compared with the old group who received SE (GVI) and the control young group (GI) (p < 0.05). On the other hand, there was a significant excess in the TNF-𝛼 and IL-1𝛽 levels of the UVA-irradiated group (GIII) group when compared with both of control group and UVA+ SE treated group (GIV) (𝑝 <0.05). Prominently, SE suppressed the (TNF-𝛼 and IL-1𝛽) levels and restore them to control levels. The same results were represented in the group of control old rats (GV) when compared with the old treated group (GVI) and control young group (GI) (p<0.05) (Table 1).

Physiological study (Collagen biosynthesis)

As shown in Table (1), Figure (5A), the levels of Hyp were significantly decreased in the UVA-irradiated group (GIII) compared to the control group (GI) (P <0.05). Meanwhile, compared to the UVA-irradiated group and the control old group, young and old rats administered SE (GII, GVI) exhibited significantly higher levels of Hyp (P <0.05). The MMP-1 content of skin tissue homogenate increased significantly in the UVA group (GIII) when compared with the control group (GI) while decreasing significantly in the UVA+ SE group (GIV) (Table 1, Fig. 5B). Dramatically reduced levels of MMP-1 in old rats treated with SE (GVI) than in the old untreated group (GV) returned to levels of control young rats (GI) (P<0.05).

Correlation analysis:

To determine how strongly two quantitative variables are associated. The correlation coefficient (r) describes how one variable moves in relation to another. Its values can range from -1 to 1. When the points are near the line of best fit, r > 0.5 or -0.5 denotes a strong correlation. The strongest relationships between the biomarkers that were found in our investigation, which were represented by ROS, TNF-α and MMP-1, deserve special attention (Fig. 6A&B). SOD showed a significant negative correlation with IL1β and MMP-1 (Fig. 6C&G). Significant negative correlation between GSH and TNF-α was demonstrated (Fig. 6E). Hyp showed a significant negative correlation with MMP-1 (Fig. 6F).

Skin is considered the first immune barrier to prevent infection and invading foreign organisms. Aging is associated with wrinkles, a thinning of the skin, loss of elasticity, delayed wound healing, and dryness [6]. There is a demand for the identification of novel sustainable raw materials and active compounds with moisturizing and wrinkle-reduction properties for a youthful appearance. Recently, studies on the anti-aging impacts of algae, such as Spirulina, have received great interest [25]. There were no toxic impacts in many species of Spirulina on different organs by using acute or chronic doses [26]. According to our results, the use of the extract of Spirulina could suppress defects of skin aging due to its anti-inflammatory and antioxidant properties [14]. The current study found that both types of aging induce the production of ROS. This may deteriorate the antioxidant defense system and disturb the redox balance, resulting in oxidative stress, which is supported with previous studies [9, 27]. Although there are antioxidant systems in the skin, the high level of ROS induced by aging exceeds their capacity. However, we found the activity of SOD and levels of GSH were improved in irradiated and the old rat groups with SE treatment. These radical-scavenging and antioxidant properties of SE may be mainly due to its phycocyanin content (10.5 %) which is Spirulina major antioxidant component as determined by its action against H₂O₂and generated OH radicals. Phycocyanin had shown wound healing, antimicrobial, and anti-inflammatory properties [28]. Spirulina contains additional vitamins and minerals in addition to the antioxidant and anti-inflammatory effects of β-Carotene (120mg/100g) [14]. Skin inflammation is known to be caused by an imbalance between the production of ROS and the antioxidant defense system throughout complex pathways [29]. ROS activates mitogen-activated protein kinase (MAPK) which in turn activates nuclear factor (NF)-κB and activator protein-1 (AP-1), which leads to the release of inflammatory cytokines such as TNF-α and IL-1β [27, 30]. These inflammatory cytokines stimulate the growth of keratinocytes in the epidermis and lead to hyperplasia of the epidermal cells as shown in the UVA group, as observed by Pillai et al. [31]. Similar to previous research, in the current study, the contents of IL-1𝛽, and TNF-𝛼 were significantly increased following UV exposure. However, after administration of SE, IL-1𝛽, and TNF-𝛼 contents were remarkably reduced to approximately the control level. Our results showed that after UV irradiation, the epidermal thickness was dramatically increased and the collagen fiber bundles were degraded and tangled. The abnormal histological alterations were explained due to the overproduction of MMPs, such as interstitial collagenase-1 (MMP-1) breaking down elastin, fibrillar collagens, and other connective components, therefore the skin loses its ability to resist the stretching [32]. Berthon et al. [33] reported that the cumulating of ROS and inflammatory responses resulted in excessive MMPs. In the current study, SE suppressed the levels of MMP-1. Besides, the analysis of hydroxyproline content of skin tissue, which was regarded as characteristic amino acid of collagen and represents changes in collagen content [34].

The results indicated that the levels of Hyp were significantly improved in the SE-treated groups maintaining intact structures in the dermis and epidermis and a tight arrangement of cells. In agreement with Ragusa et al. [35], this change in collagen content can be attributed to the SE content of several bioactive compounds, particularly proteins (67.6%), which are involved in many physiological processes, including inflammation, immune response, and skin remodeling, and they also stimulate the synthesis of structural proteins (collagen and elastin). For the same purpose, a Spirulina peptide extract showed obvious dermatological effects on the inducement of fibroblast reproduction as well as on the biosynthesis of glycosaminoglycans and collagen [36]. Additionally, it has been reported that peptides extracted from Spirulina platensis have anti-skin aging effects [17].

In conclusion, the subcutaneous injection of SE significantly showed anti-aging effects, mediated by anti-oxidation, anti-inflammation and MMP-1 inhibition in chronological and photo-aged skin of albino rats. Additionally, for the first time SE was demonstrated to increase the production of collagen on both intrinsic and extrinsic aging. This suggests that SE could relieve inflammation response and promote immune protection against skin aging in addition to enhancing collagen biosynthesis. These results suggest that SE is a useful material for application in dermo-cosmetic formulations for the improvement of the epidermis structure and to conserve the skin from the devastating effects of aging and UV exposure.

Data availability

The datasets generated during and/or analyzed during the current study are available from the corresponding author on reasonable request.

Funding

The authors have not received any funds.

Consent for publication

All authors have agreed to publish this manuscript.

Competing interests

The author(s) declare no competing interests.

Author contributions statement:

K S create the idea and supervise all steps. All authors wrote the main manuscript text and H M prepared figures and tables. K H and A M reviewed the manuscript. S S saved lab space and equipment.

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Table 1 Effects of Spirulina extract (SE) on the biochemical markers of skin tissue

	GI	GII	GIII	GIV	GV	GVI
ROS	0.175±0.017^ab	0.170±0.007^b	0.214±0.003^c	0.193±0.013^a	0.202±0.016^c	0.169±0.019^b
SOD	0.545±0.020^a	0.539±0.011^a	0.382±0.048^b	0.482±0.012^c	0.502±0.044^c	0.541±0.20^a
GSH	22.406±0.947^a	21.264±1.841^a	15.880±1.548^b	22.20±1.358^a	15.954±1.914^b	20.686±1.555^a
TNF	24.256±7.801^a	21.486±6.576^a	33.278±7.320^b	22.628±4.490^a	36.258±6.637^b	17.096±3.540^a
IL-1	8.400±1.908^a	0.7.408±1.050^acd	13.972±3.554^b	9.256±2.144^a	7.780±1.068^ac	7.122±1.1148^d
Hyp	99.60±2.61^a	119.72±10.63^a	98.44±2.31^b	115.84±4.90b^ad	119.20±6.18^b	109.42±1.33^d
MMP-1	1.31±0.06^a	1.06±0.03^a	1.46±0.20^b	1.11±0.04^a	1.08±0.02^c	1.16±0.06^a

Data are presented as means ± standard deviations (n = 7). In the same raw, values with similar letters mean a non-significant difference, and values with different letters mean a significant difference. GI (Group I): control young rats, GI (Group II): young rats received SE (20 mg/ml), GIII (Group III): young rats were administered a daily dose of saline and an hour later exposed to UVR (2.16 J/cm2), GIV (Group IV): young rats received SE (20mg/ml) and an hour later exposed to UVR (2.16 J/cm2), GV (Group V): control old rats, GVI (Group VI): old rats received SE (20 mg/ml). ROS: reactive oxygen species level, SOD: The activities of superoxide dismutase, GSH: Reduced glutathione, IL-1β: Interleukin-1β, TNF-α: tumor necrosis factor-α, Hyp: the activity of Hydroxyproline and MMP-1: matrix metalloproteinase-1.

No competing interests reported.

The collagen enhancement by Spirulina extract in intrinsic and extrinsic skin aging in albino rat

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Abstract

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Introduction

Methods

Results

Discussion

Declarations

References

Tables

Additional Declarations

Status:

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