Novel formulation development from Ophiocordyceps sinensis (Berk.) for management of high-altitude maladies.

Ophiocordyceps sinensis (Berk.) is a fungus closely related to medicinal mushroom, which belongs to the family Ophiocordycipitaceae. It is a well-known and rich herbal source of bioactive active constituents. The medicinal mushroom has garnered worldwide attention owing to its multifarious bioactivities. This mushroom grows on the larva of ghost moths (Hepialidae) and produces fruiting bodies, which serve as a vital natural source of medicine and supplementary diets. On account of the diverse pharmacological and bioactive constituents present in O. sinensis, it has been established as a potential antioxidant, anticancer, antibacterial, anti-proliferative, anti-inflammatory agent that has been successfully used for treating several health issues, including hypoxia-related problems encountered by mountaineers, pilgrims, tourists and soldiers occurring at high-altitude regions such as acute mountain sickness (AMS), high-altitude pulmonary edema (HAPE), high-altitude cerebral edema (HACE), frostbite, chilblains, hypothermia, etc. The most important pharmacologically active compounds present in the O. sinensis include nucleobases and its derivatives (adenosine, cordycepin, 3-deoxyadenosine, AMP, GMP, UMP, guanosine, uridine), polysaccharides (mannose, glucose, galactose, rhamnose, arabinose, xylose, galactose), proteins, peptides and steroids. This article focuses on the various research endeavors undertaken to scientifically establish the medicinal properties of O. sinensis, highlighting the various principally active compounds, their pharmacological action, drug designing and development and future perspective for various health benefits.

Bioactive Fractions from the Chinese Caterpillar Mushroom, Ophiocordyceps sinensis (Ascomycetes), Elucidate Adaptogenic Role against Hypoxia Stress.

Ophiocordyceps sinensis, a high-altitude medicinal mushroom, is widely revered in traditional medicine for its antiproliferative, antihypercholesterolemic, energy enhancement, etc. properties. These properties are attributed to the presence of steroids, terpenoids, polyphenolics, glycosides, and glycoproteins in it. The current study presents characterization of three phenolic rich fractions (PRFs) separated from aqueous extract of O. sinensis using diethyl ether and ethyl acetate. These fractions possessed considerable antioxidant potential in terms of total phenolic content, total flavonoid content, ferric ion reducing power, and free radical scavenging efficiency. Chemical characterization of the PRFs was carried out using HPTLC and GC-MS. The diethyl ether and ethyl acetate fractions elucidated appreciable antibacterial activity against Salmonella typhi. The aqueous extract and residual phenolic fraction displayed protective effect on HEK 293 cell lines against hypoxia stress and also bestowed appreciative adaptogenic role against cold, hypoxia, and restraint stress in vivo, by decreasing levels of malondialdehyde and superoxide dismutase and incrementing reduced glutathione concentrations.

Antioxidant-Rich Peptide Fractions Derived from High-Altitude Chinese Caterpillar Medicinal Mushroom Ophiocordyceps sinensis (Ascomycetes) Inhibit Bacterial Pathogens.

Ophiocordyceps sinensis (=Cordyceps sinensis), a medicinal mushroom native to the Orient, has been extensively used for the past few centuries in traditional Chinese medicine because of its immunomodulatory, antiinflammatory, and nutraceutical properties. In the present study, three antioxidant and antibacterial Ophiocordyceps peptide fractions (COPs) were separated from the Indian variety of O. sinensis on a Sephadex G-25 resin. Amide bonds in the COPs were confirmed by Fourier transform infrared spectroscopy and nuclear magnetic resonance. Cationic and hydrophobic amino acids, which are reported to be the major constituent amino acids of antimicrobial peptides, were identified in the COPs by matrix-assisted laser desorption/ionization-mass spectrometry and high-performance liquid chromatography. Putative secondary structures were predicted by circular dichroism to be ß-sheets and random coils. The COPs demonstrated substantial antioxidant potential by scavenging 2,2-diphenyl-l-picryl-hydrazyl-hydrate (median inhibitory concentration [IC50] values, 4.79-18.7 mg/mL) and 2,2'-azino-bis-3-ethylbenzothiazoline-6-sul-phonic acid (IC50 values, 4.51-14.05 mg/mL) free radicals and also by chelating heavy metal ions. Additionally, the peptide fractions were capable of significantly inhibiting bacterial pathogens viz. Escherichia coli and Salmonella typhi. The potential antibacterial mechanisms of action were established to be generation of reactive oxygen species and intracellular protein leakage within the bacterial cells.

Phenolic Rich Fractions from Mycelium and Fruiting Body of Ganoderma lucidum Inhibit Bacterial Pathogens Mediated by Generation of Reactive Oxygen Species and Protein Leakage and Modulate Hypoxic Stress in HEK 293 Cell Line.

Ganoderma lucidum (G. lucidum) fungus (Family Ganodermataceae) is widely used as a traditional medicine in China, Japan, and many Asian countries on account of its numerous medicinal properties such as antioxidant, anticancer, antimicrobial, energy enhancing, and immunostimulatory. This broad spectrum of therapeutic effects exhibited by G. lucidum is ascribed to its abundance in several classes of chemical constituents, namely, carbohydrates, flavonoids, minerals, phenolics, proteins, and steroids which possess substantial bioactivities. The aim of the current study was to prepare phenolic rich fractions (PRFs) from aqueous extract of the Indian variety of G. lucidum mycelium and fruiting body. These fractions were assessed for their antioxidant capacity by TPC (total phenolic content), TFC (total flavonoid content), FRAP (ferric reducing antioxidant power), and ABTS [2,2-azino-bis(3-ethylbenzothiazoline)-6-sulfonic acid] assays. Quantification of flavonoids and nucleobases present in the fractions was carried out by high-performance thin layer chromatography (HPTLC). The antibacterial activity of the fractions was evaluated against Escherichia coli, Salmonella typhi, and Staphylococcus aureus. The antibacterial mechanism of action of the PRFs was established to be generation of reactive oxygen species and leakage of proteins within bacterial cells. Additionally, the protective effect of the PRFs in counteracting hypoxia was observed in HEK 293 cell lines.

Augmentation of humoral and cellular immunity in response to Tetanus and Diphtheria toxoids by supercritical carbon dioxide extracts of Hippophae rhamnoides L. leaves.

Hippophae rhamnoides L. commonly known as Seabuckthorn (SBT), a wild shrub of family Elaegnacea, has extensively used for treating various ailments like skin diseases, jaundice, asthma, lung troubles. SBT leaves have been reported to possess several pharmacological properties including immunomodulatory, antioxidant, anti-inflammatory, antimicrobial and tissue regeneration etc. The present study was undertaken to evaluate the adjuvant property of supercritical carbon dioxide extracts (SCEs 300ET and 350ET) of SBT leaves in balb/c mice immunized with Tetanus and Diphtheria toxoids. The dynamic changes in the immune response were measured in terms of humoral and cell-mediated immune responses. We have seen the effect of SCEs on immunoglobulin subtypes and secondary immune response generation. In addition, the effect of SCEs on antigen specific cellular immunity was evaluated. Our results show that SCEs 300ET and 350ET significantly enhanced antibody titers in response to both TT and DT antigens. The secondary immune response generated was significantly increased in case of TT immunized animals. SCEs also enhanced cytokine levels (IFN-γ, IL-4, TNF-α and IL-1ß) and increased lymphoproliferation. Besides, both SCEs did not show any toxic effects. Therefore, the study suggests that SCEs are safe and have potent immunostimulatory activity and hence, seems to be a promising balanced Th1 and Th2 directing immunological adjuvant for various veterinary as well as human vaccines.