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[Inhibitory effects of some traditional medicines on proliferation of HIV-1 and its protease].

In attempts to discover anti-HIV agents from natural sources, various traditional medicine extracts were tested for their inhibitory effects on HIV-1 proliferation and its protease. An extract of the seeds of Croton tiglium showed potent inhibitory effects on the proliferation of HIV-1. The active principle was determined to be phorbol esters. Several derivatives of phorbol ester were evaluated for inhibition of proliferation as well as activation of protein kinase C (PKC). Of these compounds, 12-O-acetylphorbol 13-decanoate (6) showed the most potent inhibition of proliferation without activating PKC. Some triterpenes from the stems of Cynomorium songaricum and the woody part of Xanthoceras sorbifolia showed inhibitory activity against HIV-1 protease. Various derivatives of oleanolic acid were synthesized and evaluated for their inhibitory activity against HIV-1 protease. Their inhibitory mechanism was also investigated.

Croton↗

Detection and determination of chemical groups in an extract of Allophylus cominia (L.).

The preliminary chemical characterization of the aqueous extract of Allophylus cominia (L.) Sw leaves was carried out by a phytochemical screening, the determination of the protein concentration by Lowry's method, as well as the composition of fatty acids and carbohydrates by gaseous chromatography (GC). The presence of the free amine groups, free phenolics, tannins, leucoantocianidines, saponines, triterpens, and steroids was detected. The concentration of proteins were 6.22 mg/mL. The composition of fatty acids (%) were: lauric acid (C12): 1.87; miristic acid (C14): 9.13; palmitic acid (C16): 19.87; stearic acid (C18): 8.35; and araquidic acid (C20): 7.83. The identified carbohydrates (mg/mg totals) were: arabinose: 0.06; xilose: 0.025; galactose: 0.241; and glucose: 1.2. Some members of these analyzed groups are reported in literature as potent hypoglycemic agents. For this reason, the presence of these substances in the analyzed extract may be one of the factors that contribute to the pharmacological effect of their administration in experimental diabetic models.

Humans↗

Effects of Cassia auriculata and Cardospermum halicacabum teas on the steady state blood levels of theophylline in rats.

The effects of concurrent administration of herbal tea prepared from dried flowers of Cassia auriculata or aerial parts of Cardospermum halicacabum and steady state serum levels of theophylline was investigated in Wistar rats. Results obtained demonstrate that a significant increase in the steady state levels of theophylline occur when this drug is administered concurrently with herbal tea prepared from either of the above plants. C. auriculata and C. halicacabum enhanced the steady state levels of theophylline by 32.5% (p < 0.02) and 48.2% (p < 0.02), respectively, when compared with the levels in animals receiving theophylline alone for the same time period. Herbal teas prepared from C. auriculata or C. halicacabum should therefore be avoided by patients treated with theophylline as these herbal teas have the potential to influence the bioavailability of the prescription drug.

Animals↗

[Toxicity of the ethanol extract of Magonia pubescens on larvae Aedes aegypti].

Crude ethanol extracted from Magonia pubescens trunks was utilized to prove its effect in the intestinal tract of Aedes aegypti 3rd instar larvae. Exposure times (2, 4, 6, 8, 10, 12, and 13 hours) were tested to verify when the morphological alterations begin to occur, in the intestinal tract of the larvae. The toxic effect of the extract was mainly in the midgut, beginning at the anterior midgut and followed through to posterior midgut. The main alterations observed were partial or total cell destruction, high citoplasmatic vacuolization, increase of subperitrophic space, cell hypertrophy and the epithelium did not maintain its monolayer appearance. The alterations began after four hours of exposure to M. pubescens extract. Observations of tissue sections from larvae treated for different lengths of time revealed a wide variation in the degree of damage between exposure periods and midgut larvae region. The present study provides evidence regarding the mode of action of the M. pubescens extract and suggests its potential utilization as a larvicide to control Aedes aegypti mosquito.

Aedes↗

Field infestation of rambutan fruits by internal-feeding pests in Hawaii.

More than 47,000 mature fruits of nine different varieties of rambutan (Nephelium lappaceum L.) were harvested from orchards in Hawaii to assess natural levels of infestation by tephritid fruit flies and other internal feeding pests. Additionally, harvested, mature fruits of seven different rambutan varieties were artificially infested with eggs or first-instars of Mediterranean fruit fly, Ceratitis capitata (Wiedemann), or oriental fruit fly, Bactrocera dorsalis (Hendel) (Diptera: Tephritidae) to assess host suitability. When all varieties were combined over two field seasons of sampling, fruit infestation rates were 0.021% for oriental fruit fly, 0.097% for Cryptophlebia spp. (Lepidoptera: Tortricidae), and 0.85% for pyralids (Lepidoptera). Species of Cryptophlebia included both C. illepida (Butler), the native Hawaiian species, and C. ombrodelta (Lower), an introduced species from Australia. Cryptophlebia spp. had not previously been known to attack rambutan. The pyralid infestation was mainly attributable to Cryptoblabes gnidiella (Milliere), a species also not previously recorded on rambutan in Hawaii. Overall infestation rate for other moths in the families Blastobasidae, Gracillariidae, Tineidae, and Tortricidae was 0.061%. In artificially infested fruits, both species of fruit fly showed moderately high survivorship for all varieties tested. Because rambutan has such low rates of infestation by oriental fruit fly and Cryptophlebia spp., the two primary internal-feeding regulatory pests of rambutan in Hawaii, it may be amenable to the alternative treatment efficacy approach to postharvest quarantine treatment.

Animals↗

Accelerated development of quarantine treatments for insects on poor hosts.

The probit 9 standard for quarantine treatment efficacy (99.9968% mortality) was originally recommended for tropical fruits heavily infested with fruit flies and it centers on high mortality to achieve quarantine security. This standard may be too stringent for quarantine pests in commodities that are rarely infested or are poor hosts, The alternative treatment efficacy approach measures risk as the probability of a mating pair, gravid female, or parthenogenic individual surviving in a shipment. This will be a function of many factors including infestation rate and shipment volume. Applying the risk-based alternative treatment efficacy approach to pests on rarely infested or poor hosts will lower the number of required test insects needed for developing quarantine treatments; hence data for a quarantine treatment could be generated by testing 10,000 or fewer insects with no survivors, compared with 90,000-100,000 insects to demonstrate the traditional probit 9 efficacy. Several commodity/quarantine pest systems where this approach could be applied are discussed. This approach would save time and resources, and help farmers export their crop on a more-timely basis.

Animals↗

Hot water immersion to ensure quarantine security for Cryptophlebia spp. (Lepidoptera: Tortricidae) in lychee and longan exported from Hawaii.

We determined whether immersion in 49 degrees C water for 20 min, a quarantine treatment developed for disinfestation of fruit flies in lychee, Litchi chinensis Sonn., and longan, Dimocarpus longan (Lourd.) Steud., exported from Hawaii, would also disinfest fruit of two species of Cryptophlebia. The pattern of tolerance to heat in Cryptophlebia illepida (Butler) was generally eggs < neonates < early instars = late instars < pupae. No C. illepida survived immersion for 16 or 20 min. Late fourth and fifth instars were determined to be the most tolerant stage that occurs in harvested fruit. Late instars of Cryptophlebia ombrodelta (Lower) were more tolerant of hot-water immersion than those of C. illepida, but no C. ombrodelta late instars survived immersion for 16 or 20 min. The hot water immersion quarantine treatment for fruit flies should effectively disinfest lychees and longans of any Cryptophlebia.

Animals↗

Isolation, identification, and characterization of compounds from acer rubrum capable of oxidizing equine erythrocytes.

OBJECTIVE: To identify compounds in Acer rubrum that cause hemolysis or oxidation of equine erythrocytes and determine whether these toxins are found in other Acer spp. SAMPLE POPULATION: Equine erythrocytes. PROCEDURE: Washed erythrocytes were incubated with extracts and fractions of Acer spp that were separated by thin layer chromatography. Methemoglobin and hemolysis were measured spectrophotometrically. Compounds within Acer spp fractions associated with cell oxidation or hemolysis were identified by gas chromatography-mass spectrometry. RESULTS: Erythrocytes incubated separately with either A. rubrum, A. saccharum, or A. saccharinum extracts had increased methemoglobin formation, compared with extract-free control samples. Two Acer spp fractions had toxic effects on erythrocytes in vitro. A major component of the Acer fraction that caused a significant amount of methemoglobin formation was identified as gallic acid. An amount of gallic acid equivalent to that found in A. rubrum extract significantly increased methemoglobin, compared with extract-free control erythrocytes, but caused less methemoglobin formation than A. rubrum extracts did. A potential co-oxidant, 2,3-dihydro-3,5-dihydroxy-6-methoxy-4H-pyran-4-one, was found in the A. rubrum extract and may have been responsible for increasing methemoglobin formation. A second A. rubrum fraction caused methemoglobin formation and significant hemolysis. A. saccharum and A. saccharinum extracts caused hemolysis but less than the A. rubrum extracts did. CONCLUSION AND CLINICAL RELEVANCE: Oxidants in A. rubrum are also found in A. saccharum and A. saccharinum, and the ingestion of A. saccharum and A. saccharinum poses a potential threat to horses.

Animals↗

Regeneration of plantlets in Sapindus trifoiatus L.

Continuous production of healthy plantlets of Sapindus trifoliatus L. was achieved via somatic embryos from long term cultures of an embryogenic mass (EM). A highly embryogenic culture of S. trifoliatus L. was obtained by recurrent embryogenesis from somatic embryos cultured on Murashige and Skoog's (MS) medium supplemented with kinetin (2.3 microM) and benzyladenine (8.8 microM). The cultures could be maintained without reduction of embryogenic competence for more than 20 months by subculture at 4 week intervals. About 90% mature somatic embryos on transfer to basal MS medium, germinated to plantlets, of which more than 70% survived when transferred to a sand and soil mixture in green house.

Plant Leaves↗

[Effects of magnesium deficiency on senescence of Dimocarpus longana leaves].

180 days old Dimocarpus longana seedlings were grown in nutrition solution with three magnesium concentrations as 4 mmol.L-1 Mg2+ (sufficient supply), 0.4 mmol.L-1 Mg2+ (deficient supply), and Mg-free (without supply). Leaves were sampled 120 and 150 days later after treatment. With an increase in severity of Mg-deficient, the chlorophyll content, PS II activities, photosynthetic rate, protein, nucleic acid (DNA, RNA), and ZRs contents declined progressively. Whereas the content of H2O2, the rate of O2-. generation as well as the content of malondialdehyde (MDA) increased. The results suggested that magnesium deficiency had significant effect on the senescence of Dimocarpus longana leaves.

Aging↗

[Regulation function of calcium on photosynthesis of Dimocarpus longana Lour. cv. wulongling under simulated acid rain stress].

Studies on the regulation function of calcium on photosynthesis of Dimocarpus longana under simulated acid rain stress showed that the photoreduction activity of chloroplasts was activated when the concentration of calcium ion in reaction medium ranged from 0 to 5 mmol.L-1, and peaked at the 3.5 mmol.L-1, which was 41.90% higher than that of control. Conversely, the activity of chloroplasts reduced 26.06% in the reaction medium with a concentration of 2 mmol.L-1 EGTA, as compared with the control. Both Mn2+ and Mg2+ could inhibit photoreduction activity. The photophosphorylation activity increased when the concentration of calcium ion in reaction medium ranged from 0 to 6 mmol.L-1, and peaked at the 4.5 mmol.L-1, while superoxidase dismutase (SOD) activity rose from 0 to 6 mmol.L-1 and peaked at 6 mmol.L-1. Calcium ion with the concentration of both 10 mmol.L-1 and 15 mmol.L-1 could increase the content of chlorophyll(Chl), stabilize the membrane structure of leaf discs, and reduce the membrane permeability under simulated acid rain with pH value of 3.0. The effect in 15 mmol.L-1 were better than in 10 mmol.L-1. However, the injury of acid rain to leaves was strengthened when the concentration of calcium was higher than 20 mmol.L-1. Net photosynthesis rate (Pn) rose when leaves sprayed with 15 mmol.L-1 Ca(NO3)2 before treatment of acid rain stress of pH 2.5. All of the results represented the excellent protection function of calcium on D. longana leaves under simulated acid rain.

Acid Rain↗

[The relationship between the desiccation-induced browning and the metabolism of active oxygen and phenolics in pericarp of postharvest longan fruit].

Longan (Dimocarpus longan Lour.) fruits are very susceptible to water loss and pericarp browning, and postharvest pericarp browning is the most important factors degrading the quality of longan fruit and shorting storage life. Pericarp browning has been attributed to desiccation, chilling, heat stress, senescence and pest or pathogen attack. Desiccation is the most main factor of induced-pericarp browning in longan. The relationship between water loss from pericarp and pericarp browning in longan cv. Fuyan fruits using open plastic punnets and sealed polyethylene bags at 10 degrees C +/-1 degrees C and 50% relative humidity, and the effect of pericarp water loss of the fruit on active oxygen metabolism and phenolics metabolism were investigated. Water loss resulted in rapid pericarp browning. Development of pericarp browning was higher with higher rate of water loss from pericarp and storage time (from 0 to 6 days). Water loss from pericarp was positively correlated with pericarp browning index significantly (P<0.01). Water loss from pericarp resulted in reduced activities of reactive-oxygen-scavenging enzymes (SOD, CAT, APX and GR), decreased amounts of endogenous antioxidant substances (AsA and GSH), and increased rates of O(-.)(2) production, MDA content and relative leakage rate, which showed that membrane structure was broken. Water loss from pericarp resulted in an increase in activity of PPO, and obvious reductions in total phenolic and flavonoid contents, whereas there was not obvious change in anthocyanin content. These results show that phenolics and flavonoids are the main substrates for PPO during desiccation-induced browning. Water loss from pericarp caused a significant increase in activity of POD, which also plays an important role in desiccation-induced browning in pericarp of longan fruit. Water loss from pericarp caused an increase in pH value, which resulted in changes in anthocyanin structure and color, the degradation of anthocyanin became easier. The results suggest that desiccation-induced browning of longan pericarp may be due to a decrease in activities of reactive-oxygen-scavenging enzymes and amounts of endogenous antioxidant substances, an accumulation of active oxygen, an increase in membrane lipid peroxidation, an injury of the integrity of cellular membrane structure, which, in turn, may cause cellular decompartmentation, resulted in PPO and POD, located in plastid and other organelle, to come into contact with phenolic and flavonoid substrates, located in vacuole, to form brown polymers.

Catalase↗

Biochemical studies of embryogenic and non-embryogenic callus of Cardiospermum halicacabum L.

Some physiological and biochemical changes were measured between embryogenic and non-embryogenic callus obtained from Cardiospermum halicacabum. Combination of auxin with cytokinin was more favourable for high amount of callus formation. 2,4-D played a key role in triggering somatic embryo formation. Embryogenic callus had more total carbohydrate and starch contents, total free amino acids, nucleic acids, phenols and ascorbic acid. Non-embryogenic callus exhibited high chlorophyll content, total soluble sugar, protein, ammonia and enzymes like peroxidase and polyphenol oxidase. Thus, the present study indicated that the process of somatic embryogenesis was characterized by some biochemical and physiological changes induced by plant growth regulators.

Carbohydrates↗

[The extraction and identification of total flavanone from longan pericarp].

OBJECTIVE: In order to make use of the resources of total flavanone in pericarp of longan. METHODS: The flavonids were extracted with ethanol. Used spectrophotometry to check the flavanone. RESULTS: The total flavanone in the pericarp was 1.101 mg/ml and the rate of recovery was 99.98%. CONCLUSION: The extraction and purifying methods in this experiment can get the outcome and the purity of the flavanone very high. This method is a purely physical process and has not any pollution. It is an ideal way to extract the flavanone of longan skin.

Drugs, Chinese Herbal↗