| Literature DB >> 35681343 |
Yaxi Zhou1,2, Shiqi Zhou1,2, Hao Duan1,2, Jing Wang3, Wenjie Yan1,2.
Abstract
Silkworm pupae are insects that are beneficial to human health, not only for their high nutritional value but, more importantly, for the variety of pharmacological functions they can perform when consumed. Currently, there is a lot of interest in the pharmaceutical applications of silkworm pupae. In recent years, the biological functions of domestic silkworm pupae have gradually been identified and confirmed, especially for their beneficial effects on human health. Studies have found that silkworm pupae have positive effects on liver protection, immune enhancement, antiapoptosis, antitumour, antibacterial, regulation of blood glucose and blood lipids, and lowering of blood pressure. However, the pharmacological mechanisms and systemic safety of silkworm pupae have not been systematically evaluated. In this paper, the nutritional composition of the pupae of the domestic silkworm is first summarised. The pharmacological functions of silkworm pupae and their components are then classified, and their mechanisms of occurrence are described. In addition, we provide a preliminary evaluation of the safety of silkworm pupae, analyse their application prospects, and suggest future directions for further pharmacological function studies. The aim is to generate interest in the promotion of human health through the use of silkworm pupae.Entities:
Keywords: applications; composition; functions; silkworm pupae
Year: 2022 PMID: 35681343 PMCID: PMC9180533 DOI: 10.3390/foods11111594
Source DB: PubMed Journal: Foods ISSN: 2304-8158
Figure 1The life cycle of the silkworm.
Amino acid composition of different varieties of silkworm pupae proteins [9,21,22,24].
| Amino Acid |
| Mulberry Silkworm Pupae |
| Hen Egg | |
|---|---|---|---|---|---|
| Asp | 9.1 | 9.89 | 10.9 | 6.41 | 8.92 |
| Thr | 3.9 | 4.75 | 5.4 | 4.64 | 4.47 |
| Ser | 3.7 | 5.25 | 4.7 | 4.64 | 6.72 |
| Glu | 9.5 | 12.9 | 14.9 | 12.74 | 12.13 |
| Gly | 3.6 | 4.94 | 4.6 | 4.42 | 3.02 |
| Ala | 3.9 | 6.05 | 5.5 | 6.26 | 5.03 |
| Cys | 1.4 | 0.53 | 1.4 | 1.5 | 1.90 |
| Val | 4.7 | 5.36 | 5.6 | 6.63 | 5.42 |
| Met | 3.4 | 2.31 | 4.6 | 1.47 | 2.81 |
| Ile | 3.4 | 4.42 | 5.7 | 7.95 | 4.88 |
| Leu | 6.2 | 6.63 | 8.3 | 3.24 | 8.11 |
| Tyr | 5.6 | 6.4 | 5.4 | 2.06 | 3.81 |
| Phe | 4.6 | 5.24 | 5.1 | 8.10 | 4.82 |
| Lys | 6.1 | 6.54 | 7.5 | 4.54 | 6.59 |
| His | 2.7 | 2.67 | 2.5 | 2.94 | 2.09 |
| Arg | 4.7 | 4.41 | 6.8 | 4.12 | 5.70 |
| Pro | 7.0 | 6.46 | 4.0 | 12.22 | 3.38 |
| Trp | 1.5 | NA | 0.9 | 4.05 | 1.72 |
Values are expressed as g/100 g of protein. NA: Data not available.
Fatty acid composition of different varieties of silkworm pupae oil [9,12,19,26,27,28].
| Fatty Acids | Chemical |
| Mulberry Silkworm Pupae |
| Sunflower Oil | |
|---|---|---|---|---|---|---|
| Myristic acid (C14:0) |
| 0.1 | ND | 0.18 | NA | NA |
| Palmitic acid (C16:0) |
| 24.2 | 26.98 | 23.18 | 17.25 | 5.6 |
| Palmitoleic acid (C16:1) |
| 1.7 | 1.82 | 1.07 | 1.14 | NA |
| Stearic acid (C18:0) |
| 4.5 | 4.73 | 4.69 | 2.23 | 2.2 |
| Oleic acid (C18:1) |
| 26.0 | 15.89 | 28.32 | 29.15 | 25.1 |
| Linoleic acid (C18:2) |
| 7.3 | 5.49 | 3.88 | 7.14 | 66.2 |
| α-Linolenic acid (C18:3) |
| 36.3 | 44.73 | 38.25 | 40.28 | NA |
| Saturated fatty acids | — | 28.8 | 31.71 | 28.05 | 19.48 | 7.8 |
| Monounsaturated fatty acids | — | 27.7 | 17.71 | 29.39 | 30.29 | 25.1 |
| Polyunsaturated fatty acids | — | 43.6 | 50.22 | 42.13 | 47.42 | 66.2 |
Values are expressed as a percentage of fatty acids. NA: data not available.
Mineral composition of different species of silkworm pupae [21,22,24,35].
| Minerals |
|
| |
|---|---|---|---|
| Phosphorus | 474 | 584 | 272 |
| Iron | 26 | 24 | 4 |
| Calcium | 158 | 74.2 | 63 |
| Zinc | 23 | 7.24 | 3.57 |
| Copper | 0.15 | 1.75 | 0.73 |
| Magnesium | 207 | 178 | 154 |
| Manganese | 0.71 | 2.54 | NA |
| Chromium | 1.69 | NA | 9.84 |
Values are expressed as mg/100 g dry weight. NA: data not available.
Pharmacological functions and mechanisms of occurrence of silkworm pupae.
| Pharmacological Functions | Species of Silkworm Pupae | Functional Ingredients | Cell Line/Animal Model or Method | In Vivo or In Vitro | Occurring Mechanism | Evaluation of Research Findings | Reference |
|---|---|---|---|---|---|---|---|
| Antitumor |
| Protein hydrolysates | Human gastric cancer SGC-7901 cells | In vitro | Inhibits the proliferation of human gastric cancer cells SGC-7901 and stimulates their abnormal morphological features; induces apoptosis and blocks the cell cycle in S phase; causes the accumulation of ROS and depolarisation of the mitochondrial membrane potential. | Silkworm pupae could be a source of anticancer drugs in the future. | [ |
|
| Protein hydrolysates | MGC-803 gastric cancer cells | In vitro | Structural changes in intracellular organelles, including mitochondrial swelling, vacuolisation and rupture. Impact on the metabolic energy supply of MGC-803 cells. | Represents a potential chemotherapy candidate for the treatment of gastric tumours. | [ | |
| Protein extracts | Breast cancer cells MCF-7 | In vitro | MCF-7 cells had significantly lower protein and nucleic acid content, as well as significantly lower IL-6, IL-1, and TNF- levels. | May provide a potential novel therapeutic target for breast cancer. | [ | ||
|
| Se-rich amino acids | Human hepatoma cells | In vitro | Significantly and dose-dependently inhibits cell viability, induces changes in cell morphology and cycle, and causes apoptosis. It induces apoptosis through the production of ROS. | It could be used as an anticancer medicine or as a food source of necessary amino acids and trace elements for everyday health. | [ | |
| Antioxidant |
| Methanolic pupae extract | — | In vitro | Free-radical scavenging activity that is dose-dependant. | — | [ |
|
| Protein hydrolysates | — | In vitro | ABTS free-radical scavenging activity is strong. | Potential usage as a natural antioxidant in functional foods to help prevent diseases caused by oxidative stress. | [ | |
|
| Protein hydrolysates | Hepatic HepG2 cells | In vitro | In HepG2 cells, the antioxidant activity was highest (ROS reduction, superoxide dismutase expression, and glutathione synthesis activity). | May have potential as natural antioxidants. | [ | |
| Polyphenols | — | In vitro | High ROS scavenging activity was observed. | Effective as a natural antioxidant in the development of protein-rich foods. | [ | ||
| — | 30% ethanol extract | HepG2 cells | In vitro | Scavenging action against DPPH and ABTS; helping remove ROS. | Silkworm pupae can be used to generate culinary ingredients and functional materials. | [ | |
| Antibacterial |
| Chitin and chitosan | In vitro | Antifungal activity is comparable to, if not superior to, commercially available chitosan. Bacterial inhibition was greatest between 1 and 2 h and began to achieve saturation after 24 h. | Silkworm pupae are a renewable and sustainable source of chitosan that may be used in both food and medicine. | [ | |
|
| Peptides | — | In vitro | The Peptide Ranker and the CAMP (Collection of Anti-Microbial Peptides) database found peptide sequences with potential bioactivity with the highest score. | It can be utilised as a high-quality protein source. | [ | |
|
| Oil | In vitro | Gram-positive | Silkworm pupae oil can be used as an effective antibacterial agent. | [ | ||
| Antiapoptotic |
| Silkworm Protein 30Kc6 | The in vitro cell apoptosis model of HUVEC that was induced by oxidised low-density lipoprotein. | In vitro | Cell-mitogen-activated protein kinases (MAPK), particularly JNK and p38, were activated by oxidised low-density lipoprotein; 30Kc6 prevented oxidised low-density lipoprotein-induced cell death in HUVEC cells by blocking MAPK signalling pathways. | It has the potential to provide crucial information for human cardiovascular disease prevention and treatment. | [ |
|
| Silkworm haemolymph | Insect cells (Sf 9) infected with baculovirus (AcNPV) | In vitro | The silkworm’s haemolymph may directly affect the baculovirus-induced apoptosis cascade or promote the expression of antiapoptotic baculovirus genes such as p35. | Antiapoptotic components can be found in silkworm haemolymph. | [ | |
|
| Recombinant 30 K protein | HeLa cells; Spodoptera frugiperda (Sf9) | In vitro | In human and insect cells, recombinant 30 K protein prevents apoptosis triggered by viruses or chemicals. | A number of human disorders linked to apoptosis may benefit from the use of recombinant 30 K protein. | [ | |
|
| Silkworm haemolymph | The vaccinia virus–HeLa cell system | In vitro | Silkworm haemolymph inhibited apoptosis, which reduced cell detachment from an adhering surface. | In commercial animal cell cultures, silkworm pupae haemolymph is helpful in preventing cell death. | [ | |
| Blood pressure reduction | — | Peptide hydrolysates | Spontaneously hypertensive rats | In vivo | In the treated group, there was a dose-related drop in systolic blood pressure. In normal and non-hypertensive rats, peptide hydrolysate had no effect on systolic blood pressure. | The peptide hydrolysate in silkworm pupae protein possesses antihypertensive effect that is both safe and healthy, which will aid in the investigation of silkworm protein peptides as a functional component of antihypertensive therapy. | [ |
|
| Protein hydrolysates | RP- HPLC | In vitro | Angiotensin I-converting enzyme inhibitory action is found in silkworm protein hydrolysates. | Angiotensin I-converting enzyme inhibitor medicines could come from this source. | [ | |
|
| Protein hydrolysates | RP- HPLC | In vitro | With a half-inhibitory concentration of 102.15 M, the tripeptide inhibited the angiotensin-converting enzyme; the mode of angiotensin-converting enzyme inhibition was competitive. | It can be utilised in antihypertensive supplemental therapy foods as a functional element. | [ | |
|
| Protein hydrolysates | HPLC | In vitro | By flexible docking calculation, the peptide inhibitory activity was 0.047 mg/mL in IC50, and it was bound to Asp415, Asp453, Thr282, His 353, and Glu162 in the hydrogen bond to the angiotensin-converting enzyme active pocket. | It could be a good idea to look into functional foods that have antihypertension bioactivity. | [ | |
| Blood lipid reduction; |
| Protein hydrolysates | 3T3-L1 cells | In vitro | Upregulation of GLUT4 increases glucose absorption, whereas upregulation of leptin lowers fat storage. | For the first time, silk protein hydrolysate decreased fat accumulation by affecting leptin up-regulation during 3T3-L1 preadipocyte development into fibroblasts. | [ |
|
| Peptides | 3T3-L1 preadipocytes | In vitro | Adipogenesis is inhibited when adipogenic gene expression and protein synthesis are blocked, resulting in a decrease in body weight gain. | Alternatives to reduce dietary obesity that have no negative effects could be viable options. | [ | |
| — | Oil | Sprague– Dawley rats | in vivo | Consumption of silkworm pupae stimulates fat metabolism, lowering blood lipid levels. | The consumption of silkworm pupae reduces fat storage, which is thought to be useful in the prevention of metabolic syndrome. | [ | |
| Blood glucose regulation |
| Soluble fibroin | 3T3-L1 adipocyte | in vitro | In 3T3-L1 adipocytes, fibronectin promotes glucose absorption and metabolism. | This could explain why the body’s response to fibre improves diabetic hyperglycaemia. | [ |
|
| Purified fibroin | A Spanish hybrid of silkworm races (Sierra Morena X Bagdad) | In vivo | The findings show a decrease in glucose levels in the haemolymph. | Diabetes, obesity, and other lifestyle-related disorders may benefit from this supplement. | [ | |
|
| Protein | Male C57BL/6 mice | in vivo | The protein from silkworm pupae lowers blood glucose levels considerably. | — | [ | |
| Cardiovascular protection |
| Crude extract | Male New Zealand white rabbits | in vivo | The size of the atherosclerotic plaques was reduced histopathologically. | There is a scientific basis for naming | [ |
| — | Silkworm pupae oil sodium salt | Rat VSMCs cells | In vitro | ERK1/2 phosphorylation was downregulated in PDGF-bb-stimulated VSMCs, which inhibited PDGF-bb-induced cell migration and proliferation. | As a functional food and medicine, it could be beneficial in the treatment of vascular problems. | [ | |
|
| Silkworm Protein 30Kc6 | In vivo atherosclerosis rabbit model | In vivo | It reduced serum levels of total triglycerides (TGs), high-density lipoprotein cholesterol (HDL-C), low-density lipoprotein cholesterol (LDLC), and total cholesterol (TC) in atherosclerotic rabbits, improving their condition. | Providing critical information for the prevention and treatment of human cardiovascular disease. | [ | |
| Liver protection |
| Oil | Acetaminophen-induced acute | In vivo | Silkworm pupa oil reduced MDA levels while enhancing SOD and GSH-Px activity, preventing APAP-induced oxidative stress. Overall, silkworm pupa oil protected against APAP-induced liver injury, which was related to the suppression of the oxidative stress-mediated NF-B signalling pathway; SPO also protected against APAP-induced liver injury. | Silkworm pupa oil supplementation could be a viable treatment option for acute liver damage. | [ |
|
| Fermented silkworm powder | Sprague–Dawley rats | In vivo | It significantly reduces hepatic alcohol dehydrogenase and acetaldehyde dehydrogenase activity and significantly increases serum AST, g-GTP, and LDH activity, as well as blood alcohol and acetaldehyde levels. | A promising pharmacological candidate for the prevention of hepatotoxicity and oxidative stress caused by alcohol. | [ | |
| Treatment of gastric ulcers |
| Oil | Hydrochloric acid/ethanol-induced | In vivo | Gastric ulcer area and secretions were reduced by silkworm pupae oil, but gastric pH increased. SOD, CAT, GSH-Px, SST, and VIP serum levels increased, while IL-6, IL-12, TNF-α, IFN-γ, MTL, and GT serum levels dropped. Meanwhile, EGF, EGFR, VEGF, and eNOS expressions were increased, while NF-κB, Bcl-2, COX-2, and iNOS expressions were decreased. | In mice, silkworm pupa oil decreased oxidative damage and inflammation. | [ |
| Immune regulation |
| Polysaccharide | Penaeid prawns | In vivo | Innate immunity is turned on. | In penaeid prawns, it effectively inhibits vibriosis. | [ |
|
| Peptides | Mouse spleen cells | In vitro | Immune-related factors such as interleukin-6 and interleukin-12, nuclear factor-B, cyclin D1, and cyclin-dependent kinase 4 are all stimulated. | Silkworm pupae polysaccharides have an immunomodulatory function and may have medicinal promise. | [ | |
| Antigenotoxic |
| — | Normal human leukocytes; Comet assay | In vitro | At a dosage of 1 mg/mL, pupae extract protects against hydrogen peroxide-induced DNA damage. | The inclusion of polyphenolic groups and fatty acids such as linoleic acid may explain pupae’s antigenotoxic activity. | [ |
| As bioreactor |
| — | Silkworm pupae | In vivo | Silkworm nucleopolyhedrosis virus was used to successfully express the human granulocyte-macrophage colony-stimulating factor in silkworm pupae. | For heterologous protein expression, the silkworm pupa is a convenient and low-cost bioreactor. | [ |
| Antifatigue |
| Powders of silkworm, pupae, dongchunghacho, and silk powder | ICR mice | in vivo | Increases swimming time and muscle mass in mice while reducing tiredness. | It has antifatigue properties and may help athletes perform better. | [ |
| Anti-Alzheimer’s disease |
| Silkworm pupa vaccine | Transgenic mouse model of AD | In vivo | Recombinant proteins synthesised in domestic silkworm pupae reduced brain deposition, lowered malondialdehyde levels, and improved memory and cognitive performance in mice. | The very nutritious CTB-A15 silkworm pupae vaccine could be used to prevent Alzheimer’s disease in the future. | [ |
|
| Silkworm pupae Powder | Male Wistar rats | Hippocampal memory deficit was significantly reduced in vivo, as was hippocampal neuron density. | Silkworm pupae appear to be a potentially useful meal for Alzheimer’s disease prevention. Hippocampal memory deficit was significantly reduced, as was hippocampal neuron density. | [ | ||
| Alcohol detoxification |
| Extracts | Imprinting Control Region (ICR) mice | In vivo | There is a significant increase in alcohol dehydrogenase activity in the livers of mice given 0.5 mg/mL silkworm pupae extract orally. | The positive effect of silkworm pupae extract on animal alcohol detoxification suggests that the extract could be employed as a therapeutic substance to help people avoid hangovers. | [ |
| Antiageing |
| Oils and sericin | — | Oils and sericin have tyrosinase inhibitory and free-radical scavenging properties in vitro. | Antiaging and whitening cosmetics are possible applications. | [ | |
| Inhibits the proliferation of fibroblasts | — | Carboxymethyl chitosan | Mouse L929 fibroblasts | In vitro | SP-carboxymethyl chitosan suppresses cell growth and drastically reduces TGF-β1/Smads signalling pathway gene and protein expression. | Through the TGF-β1/Smads signalling pathway, SP-carboxymethyl chitosan may impact L929 cell proliferation and inhibit postoperative adhesion. | [ |
“—” indicates not stated in the literature.
Figure 2Function and physiological mechanisms of silkworm pupae proteins.
Figure 3Function and physiological mechanisms of silkworm pupae oils.