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1.
Environ Res ; 251(Pt 2): 118664, 2024 Jun 15.
Article in English | MEDLINE | ID: mdl-38499222

ABSTRACT

The extensive use of mineral fertilizers has a negative impact on the environment, whereas wastewater and microalgal biomass can provide crops with nutrients such as nitrogen, phosphorus, and potassium, and have the potential to be used as a source of fertilizers in circular agriculture. In this study, a step-by-step resource utilization study of algae-containing wastewater generated from microalgae treatment of swine wastewater was carried out. When wheat seedlings were cultivated in the effluent after microalgae separation, the root fresh weight, seedling fresh weight, and total seedling length were increased by 3.44%, 14.45%, and 13.64%, respectively, compared with that of the algae-containing wastewater, and there was no significant difference in seedling fresh weight, total seedling length, maximum quantum yields of PSII photochemistry (Fv/Fm), and performance index (PIABS) from that of the Hogland solution group, which has the potential to be an alternative liquid fertilizer. Under salt stress, microalgae extract increased the contents of GA3, IAA, ABA, and SA in wheat seedlings, antioxidant enzymes maintained high activity, and the PIABS value increased. Low-dose microalgae extract (1 mL/L) increased the root fresh weight, seedling fresh weight, longest seedling length, and total seedling length by 30.73%, 31.28%, 16.43%, and 28.85%, respectively. Algae extract can act as a plant biostimulant to regulate phytohormone levels to attenuate the damage of salt stress and promote growth.


Subject(s)
Biomass , Microalgae , Seedlings , Triticum , Wastewater , Triticum/growth & development , Triticum/drug effects , Microalgae/growth & development , Microalgae/drug effects , Seedlings/growth & development , Seedlings/drug effects , Animals , Wastewater/chemistry , Swine , Salt Tolerance , Fertilizers/analysis , Waste Disposal, Fluid/methods
2.
Neurosci Lett ; 735: 135232, 2020 09 14.
Article in English | MEDLINE | ID: mdl-32621948

ABSTRACT

Growing evidence suggested that energy deficiency might be involved in the pathophysiological mechanism of depression. Energy deficiency, mainly results from mitochondrial damage, can lead to the dysfunction of synaptic neurotransmission, and further cause depressive-like behavior. The antidepressant effect of resveratrol had been widely demonstrated in previous studies; however, the underlying mechanism remains poorly understood. The present study aimed to investigate whether the antidepressant effects of resveratrol involved in the energy levels and neurotransmission in the hippocampus. We found that resveratrol and fluoxetine significantly attenuated depressive-like behaviors induced by chronic unpredictable mild stress (CUMS), which evidenced by the increased sucrose preference and the reduced immobility time in a forced swimming test. In addition, resveratrol increased hippocampal ATP levels, decreased Na+-K+-ATPase and pyruvate levels, and upregulated the levels of mitochondrial DNA (mtDNA), mRNA expression of sirtuin (SIRT)1 and peroxisome proliferator-activated receptor γ coactivator (PGC)1α. Furthermore, resveratrol and fluoxetine increased serotonin (5-HT) levels and downregulated the mRNA expression of 5-HT transporter (SERT) in the hippocampus. The decreased protein expression of growth-associated protein (GAP)-43 induced by CUMS was also ameliorated by resveratrol and fluoxetine. These findings demonstrated the antidepressant effects of resveratrol and suggested that resveratrol was able to promote mitochondrial biogenesis, enhance ATP and 5-HT levels, as well as upregulate GAP-43 expression in the hippocampus.


Subject(s)
Adenosine Triphosphate/biosynthesis , GAP-43 Protein/biosynthesis , Hippocampus/metabolism , Resveratrol/therapeutic use , Serotonin/biosynthesis , Stress, Psychological/metabolism , Animals , Antidepressive Agents/pharmacology , Antidepressive Agents/therapeutic use , Chronic Disease , Dose-Response Relationship, Drug , Hippocampus/drug effects , Male , Mice , Mice, Inbred ICR , Resveratrol/pharmacology , Stress, Psychological/drug therapy , Stress, Psychological/psychology , Treatment Outcome
3.
Eur J Clin Pharmacol ; 64(10): 971-7, 2008 Oct.
Article in English | MEDLINE | ID: mdl-18548239

ABSTRACT

OBJECTIVE: The findings of numerous studies have suggested that both genetic and environmental influences are involved in the pathogenesis of allergic disease and atopy. We studied the polymorphisms in the interferon (IFN)-gamma (gamma) and IFN-gamma receptor 1 (IFNR1) gene with the aim of clarifying the relationships among these polymorphisms, penicillin allergy and anti-penicillin antibodies. METHODS: A restriction endonuclease fragment length polymorphism (RFLP)-PCR analysis and sequencing were used to study the IFNR1 and IFN-gamma polymorphisms. The presence and level of eight specific immunoglobulin (Ig)E and IgG antibodies were determined by the radioallergosorbent test (RAST) and enzyme-linked immunosorbent assay (ELISA), respectively. RESULTS: The positive rates of specific IgE and IgG were 61.11 and 53.92%, respectively. There was no significant difference in the whole-allele of IFN-gamma distribution between patients with a penicillin allergy and control subjects. Allele 7 (18CA repeat) was significantly less frequent in the urticaria group (3.19 vs. 11.93%) than in the controls. There was no difference in IFN-gamma production among different alleles in IFN-gamma. The frequency of G/A (Val/Met) in the IFNR1 gene in allergic patients was significantly less than that in the controls (P < 0.05). There were no significant differences in the positive rate of IgE among different alleles of IFN-gamma. The same was true for the positive rate of IgG. CONCLUSIONS: The Met/Val allele in IFNR1 gene may have a protective role in the non-penicillin allergic population. The allele 18CA repeat in IFN-gamma gene may be associated with urticaria.


Subject(s)
Immunoglobulin E/blood , Immunoglobulin G/blood , Interferon-gamma/genetics , Penicillins/adverse effects , Receptors, Interferon/genetics , Adolescent , Adult , Aged , Aged, 80 and over , Case-Control Studies , Cohort Studies , Drug Hypersensitivity/blood , Drug Hypersensitivity/etiology , Drug Hypersensitivity/genetics , Female , Humans , Male , Middle Aged , Skin Tests/methods , Young Adult , Interferon gamma Receptor
4.
Chin Med J (Engl) ; 119(6): 458-66, 2006 Mar 20.
Article in English | MEDLINE | ID: mdl-16584643

ABSTRACT

BACKGROUND: Because of the pivotal role of the human leukocyte antigen (HLA) class II molecules in regulating the immune response and their extensive polymorphism, it is not surprising that particular HLA class II alleles have been implicated in susceptibility to allergic diseases and in restriction of the IgE responses to a variety of allergens. We investigated the relationship between HLA-DRB genotype and allergies to various penicillins and explored HLA-DRB restriction of IgE responses to these derivatives of penicillin. METHODS: Radioallergosorbent test was used to examine 8 kinds of specific IgE antibodies (4 major and 4 minor antigenic determinants) in the sera of 248 patients with an allergy to penicillins and 101 healthy subjects without any allergic reaction. Some (113 patients and 87 healthy control subjects) were chosen from all subjects to type for HLA-DRB alleles by sequence specific primer-polymerase chain reaction. RESULTS: Compared with control subjects, a significantly increased frequency of DR9 was present in 77 patients with allergic reactions, with immediate hypersensitive reaction and with urticaria (P = 0.011; P = 0.019; P = 0.005 respectively). Conversely, a significantly decreased frequency of DR14.1 was found in 80 patients with positive IgE antibodies, with immediate reaction and with urticaria compared with control group (P = 0.024; P = 0.038; P = 0.038). A possible excess of HLA-DR17 was found in subjects who were responsive to benzylpenicilloyl compared with those were not (chi(2) = 5.134, P = 0.023), and of HLA-DR4 was found in subjects responsive to phenoxomethylpenicillanyl (PVA, chi(2) = 4.057, P = 0.044). CONCLUSION: HLA-DRB gene may be involved in allergy to penicillins through modulating specific serum IgE to penicillins.


Subject(s)
Drug Hypersensitivity/genetics , HLA-DR Antigens/genetics , Immunoglobulin E/blood , Penicillins/immunology , Adolescent , Adult , Aged , Aged, 80 and over , Alleles , Child , Child, Preschool , Drug Hypersensitivity/immunology , Female , Genotype , Humans , Male , Middle Aged , Penicillins/adverse effects
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