Does Concurrent Use of Some Botanicals Interfere with Treatment of Tuberculosis?

Abstract:

:Millions of individuals with active TB do not receive recommended treatments, and instead may use botanicals, or use botanicals concurrently with established treatments. Many botanicals protect against oxidative stress, but this can interfere with redox-dependent activation of isoniazid and other prodrugs used for prophylaxis and treatment of TB, as suggested by results of a recent clinical trial of the South African botanical Sutherlandia frutescens (L.) R. Br. (Sutherlandia). Here we provide a brief summary of Sutherlandia's effects upon rodent microglia and neurons relevant to tuberculosis of the central nervous system (CNS-TB). We have observed that ethanolic extracts of Sutherlandia suppress production of reactive oxygen species (ROS) in rat primary cortical neurons stimulated by NMDA and also suppress LPS- and interferon γ (IFNγ)-induced ROS and nitric oxide (NO) production by microglial cells. Sutherlandia consumption mitigates microglial activation in the hippocampus and striatum of ischemic brains of mice. RNAseq analysis indicates that Sutherlandia suppresses gene expression of oxidative stress, inflammatory signaling and toll-like receptor pathways that can reduce the host's immune response to infection and reactivation of latent Mycobacterium tuberculosis. As a precautionary measure, we recommend that individuals receiving isoniazid for pulmonary or cerebral TB, be advised not to concurrently use botanicals or dietary supplements having antioxidant activity.

journal_name

Neuromolecular Med

journal_title

Neuromolecular medicine

authors

Folk WR,Smith A,Song H,Chuang D,Cheng J,Gu Z,Sun G

doi

10.1007/s12017-016-8402-1

subject

Has Abstract

pub_date

2016-09-01 00:00:00

pages

483-6

issue

3

eissn

1535-1084

issn

1559-1174

pii

10.1007/s12017-016-8402-1

journal_volume

18

pub_type

杂志文章,评审
  • Therapeutic strategies for the inherited neuropathies.

    abstract::More than 30 genetic causes have been identified for the inherited neuropathies collectively referred to as Charcot-Marie-Tooth (CMT) disease. Previous therapies for CMT were limited to traditional approaches such as rehabilitation medicine, ambulation aids, and pain management. Identification of the genes causing CMT...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1385/nmm:8:1-2:255

    authors: Shy ME

    更新日期:2006-01-01 00:00:00

  • Systematic Review by Multivariate Meta-analyses on the Possible Role of Tumor Necrosis Factor-α Gene Polymorphisms in Association with Ischemic Stroke.

    abstract::A number of studies have investigated the association between tumor necrosis factor (TNF)-α gene polymorphisms and ischemic stroke susceptibility. However, results of different individual studies are often inconsistent. To provide a more robust evaluation of the association between polymorphisms of the TNF-α gene and ...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,meta分析,评审

    doi:10.1007/s12017-015-8365-7

    authors: Niu YM,Weng H,Zhang C,Yuan RX,Yan JZ,Meng XY,Luo J

    更新日期:2015-12-01 00:00:00

  • Mitochondrial oxidative phosphorylation transcriptome alterations in human amyotrophic lateral sclerosis spinal cord and blood.

    abstract::Origins of onset and progression of motor neurodegeneration in amyotrophic lateral sclerosis (ALS) are not clearly known, but may include impairment of mitochondrial bioenergetics. We used quantitative PCR approaches to analyze the mitochondrial oxidative phosphorylation (OXPHOS) transcriptomes of spinal cord tissue a...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-014-8321-y

    authors: Ladd AC,Keeney PM,Govind MM,Bennett JP Jr

    更新日期:2014-12-01 00:00:00

  • Functional polymorphism of the human multidrug resistance gene (MDR1) and polydipsia-hyponatremia in schizophrenia.

    abstract::P-glycoprotein (P-gp), which is coded by the MDR1 gene, in the brain capillary endothelial cell limits the entry of many drugs including antipsychotics into the brain. The aim of this study is to examine whether a functional polymorphism, a C to T substitution at position 3435 in exon 26 of the MDR1 gene, is associate...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-008-8041-2

    authors: Shinkai T,De Luca V,Utsunomiya K,Sakata S,Inoue Y,Fukunaka Y,Hwang R,Ohmori O,Kennedy JL,Nakamura J

    更新日期:2008-01-01 00:00:00

  • Temporal and spatial expression of cyclin H in rat spinal cord injury.

    abstract::Cyclin H regulates cell cycle transitions; it always forms trimeric cyclin-dependent protein kinases (CDK)-activating kinase (CAK) complex with CDK7 and MAT1 that phosphorylates a threonine residue in the CDK2 T loop region. However, neither the expression nor function of cyclin H in the central nervous system (CNS) i...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-011-8150-1

    authors: Wu G,Cao J,Peng C,Yang H,Cui Z,Zhao J,Wu Q,Han J,Li H,Gu X,Zhang F

    更新日期:2011-09-01 00:00:00

  • The mammalian RNA-binding protein Staufen2 links nuclear and cytoplasmic RNA processing pathways in neurons.

    abstract::Members of the Staufen family of RNA-binding proteins are highly conserved cytoplasmic RNA transporters associated with RNA granules. staufen2 is specifically expressed in neurons where the delivery of RNA to dendrites is thought to have a role in plasticity. We found that Staufen2 interacts with the nuclear pore prot...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1385/NMM:6:2-3:127

    authors: Monshausen M,Gehring NH,Kosik KS

    更新日期:2004-01-01 00:00:00

  • Cytochrome C and caspase-9 expression in Huntington's disease.

    abstract::There is increasing evidence implicating apoptosis-mediated cell death in the pathogenesis of neurodegenerative diseases. One important event in the apoptotic cascade is the release of cytochrome c by mitochondria into the cytoplasm, activating caspase-9, leading to the subsequent activation of downstream executioner ...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1385/NMM:1:3:183

    authors: Kiechle T,Dedeoglu A,Kubilus J,Kowall NW,Beal MF,Friedlander RM,Hersch SM,Ferrante RJ

    更新日期:2002-01-01 00:00:00

  • Perturbed autonomic nervous system function in metabolic syndrome.

    abstract::The metabolic syndrome is characterized by the clustering of various common metabolic abnormalities in an individual and it is associated with increased risk for the development of type 2 diabetes and cardiovascular diseases. Its prevalence in the general population is approximately 25%. Central fat accumulation and i...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-008-8022-5

    authors: Tentolouris N,Argyrakopoulou G,Katsilambros N

    更新日期:2008-01-01 00:00:00

  • Scutellarin Exerts Anti-Inflammatory Effects in Activated Microglia/Brain Macrophage in Cerebral Ischemia and in Activated BV-2 Microglia Through Regulation of MAPKs Signaling Pathway.

    abstract:BACKGROUND:Scutellarin, an herbal compound, can effectively suppress the inflammatory response in activated microglia/brain macrophage(AM/BM) in experimentally induced cerebral ischemia; however, the underlying mechanism for this has not been fully clarified. We sought to elucidate if scutellarin would exert its anti-i...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-019-08582-2

    authors: Chen HL,Jia WJ,Li HE,Han H,Li F,Zhang XL,Li JJ,Yuan Y,Wu CY

    更新日期:2020-06-01 00:00:00

  • Targeted Gene Resequencing (Astrochip) to Explore the Tripartite Synapse in Autism-Epilepsy Phenotype with Macrocephaly.

    abstract::The frequent co-occurrence of autism spectrum disorders (ASD) and epilepsy, or paroxysmal EEG abnormalities, defines a condition termed autism-epilepsy phenotype (AEP). This condition results, in some cases , from dysfunctions of glial inwardly rectifying potassium channels (Kir), which are mainly expressed in astrocy...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-015-8378-2

    authors: Marchese M,Valvo G,Moro F,Sicca F,Santorelli FM

    更新日期:2016-03-01 00:00:00

  • Scutellarin as a Potential Therapeutic Agent for Microglia-Mediated Neuroinflammation in Cerebral Ischemia.

    abstract::The cerebral ischemia is one of the most common diseases in the central nervous system that causes progressive disability or even death. In this connection, the inflammatory response mediated by the activated microglia is believed to play a central role in this pathogenesis. In the event of brain injury, activated mic...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-016-8394-x

    authors: Yuan Y,Fang M,Wu CY,Ling EA

    更新日期:2016-09-01 00:00:00

  • Epileptic seizures in AD patients.

    abstract::Epileptic seizures have long been recognised as a complication of the clinical syndrome of Alzheimer's disease, particularly in advanced disease, but have hitherto been viewed essentially as epiphenomena of the neurodegenerative process. Progress with animal models of Alzheimer's disease has suggested that this view m...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-009-8076-z

    authors: Larner AJ

    更新日期:2010-03-01 00:00:00

  • Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease.

    abstract::The gene encoding alpha-T-catenin, CTNNA3, is positioned within a region on chromosome 10, showing strong evidence of linkage to Alzheimer's disease (AD), and is therefore a good positional candidate gene for this disorder. We have demonstrated that alpha-T-catenin is expressed in human brain, and like other alpha-cat...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1385/NMM:5:2:133

    authors: Busby V,Goossens S,Nowotny P,Hamilton G,Smemo S,Harold D,Turic D,Jehu L,Myers A,Womick M,Woo D,Compton D,Doil LM,Tacey KM,Lau KF,Al-Saraj S,Killick R,Pickering-Brown S,Moore P,Hollingworth P,Archer N,Foy C,Wal

    更新日期:2004-01-01 00:00:00

  • Haplotype Study in SCA10 Families Provides Further Evidence for a Common Ancestral Origin of the Mutation.

    abstract::Spinocerebellar ataxia type 10 (SCA10) is an autosomal dominant neurodegenerative disorder characterized by progressive cerebellar ataxia and epilepsy. The disease is caused by a pentanucleotide ATTCT expansion in intron 9 of the ATXN10 gene on chromosome 22q13.3. SCA10 has shown a geographical distribution throughout...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-017-8464-8

    authors: Bampi GB,Bisso-Machado R,Hünemeier T,Gheno TC,Furtado GV,Veliz-Otani D,Cornejo-Olivas M,Mazzeti P,Bortolini MC,Jardim LB,Saraiva-Pereira ML,Rede Neurogenetica.

    更新日期:2017-12-01 00:00:00

  • Mitochondrial medicine for aging and neurodegenerative diseases.

    abstract::Mitochondria are key cytoplasmic organelles, responsible for generating cellular energy, regulating intracellular calcium levels, altering the reduction-oxidation potential of cells, and regulating cell death. Increasing evidence suggests that mitochondria play a central role in aging and in neurodegenerative diseases...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-008-8044-z

    authors: Reddy PH

    更新日期:2008-01-01 00:00:00

  • A Review of Functional Electrical Stimulation Treatment in Spinal Cord Injury.

    abstract::Functional electrical stimulation (FES) has been widely adopted to elicit muscle contraction in rehabilitation training after spinal cord injury (SCI). Conventional FES modalities include stimulations coupled with rowing, cycling, assisted walking and other derivatives. In this review, we studied thirteen clinical rep...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-019-08589-9

    authors: Luo S,Xu H,Zuo Y,Liu X,All AH

    更新日期:2020-12-01 00:00:00

  • The cell biology of alpha-synuclein: a sticky problem?

    abstract::Parkinson's disease (PD) is the most common neurodegenerative motor disorder, marked by chronic progressive loss of neurons in the substantia nigra, thereby damaging purposeful control of movement. For decades, it was believed that PD was caused solely by environmental causes. However, the discovery of genetic factors...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1385/NMM:1:2:95

    authors: Cole NB,Murphy DD

    更新日期:2002-01-01 00:00:00

  • Role of Rho Kinase and Fasudil on Synaptic Plasticity in Multiple Sclerosis.

    abstract::In addition to myelin loss and oligodendrocyte injury, axonal damage is a major cause of irreversible neurological disability in multiple sclerosis (MS). A series of studies have demonstrated that Rho kinase (ROCK) is involved in synaptic plasticity of neurons. Here, we found that ROCK activity in MS serum was elevate...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-015-8374-6

    authors: Chen C,Yu JZ,Zhang Q,Zhao YF,Liu CY,Li YH,Yang WF,Ma CG,Xiao BG

    更新日期:2015-12-01 00:00:00

  • MiR-5787 Attenuates Macrophages-Mediated Inflammation by Targeting TLR4/NF-κB in Ischemic Cerebral Infarction.

    abstract::Accumulating studies have suggested the important role of microRNA (miRNA) in ischemic cerebral infarction. However, little is known of the modifying effect of miR-5787, a newly found miRNA, in ischemic cerebral infarction. We aim to elucidate the effect and underlying molecular mechanism of miR-5787 in the pathogenes...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-020-08628-w

    authors: Bao Z,Zhang S,Li X

    更新日期:2020-11-09 00:00:00

  • The molecular basis of familial dysautonomia: overview, new discoveries and implications for directed therapies.

    abstract::Familial dysautonomia (FD) is a sensory and autonomic neuropathy that affects the development and survival of sensory, sympathetic, and some parasympathetic neurons. It is autosomally inherited and occurs almost exclusively among individuals of Ashkenazi Jewish descent. The pathological and clinical manifestations of ...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-007-8019-5

    authors: Rubin BY,Anderson SL

    更新日期:2008-01-01 00:00:00

  • Structure, Distribution, and Function of Neuronal/Synaptic Spinules and Related Invaginating Projections.

    abstract::Neurons and especially their synapses often project long thin processes that can invaginate neighboring neuronal or glial cells. These "invaginating projections" can occur in almost any combination of postsynaptic, presynaptic, and glial processes. Invaginating projections provide a precise mechanism for one neuron to...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-015-8358-6

    authors: Petralia RS,Wang YX,Mattson MP,Yao PJ

    更新日期:2015-09-01 00:00:00

  • Decreased levels of circulating adiponectin in mild cognitive impairment and Alzheimer's disease.

    abstract::Adiponectin, an adipocytokine released by the adipose tissue and has important roles in the metabolic regulation and inflammatory control, may play an important roles in the physiopathology of psychiatric and neurodegenerative disorders. The aim of the present work was to evaluate adiponectin serum levels in patients ...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-012-8201-2

    authors: Teixeira AL,Diniz BS,Campos AC,Miranda AS,Rocha NP,Talib LL,Gattaz WF,Forlenza OV

    更新日期:2013-03-01 00:00:00

  • The serotonergic system and anxiety.

    abstract::The wide use of serotonin reuptake inhibitors and serotonin receptor agonists in anxiety disorders has suggested a key role for the modulatory neurotransmitter in anxiety. However, serotonin's specific role is still uncertain. This article reviews the literature concerning how and where serotonergic agents modulate an...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1385/NMM:5:1:027

    authors: Gordon JA,Hen R

    更新日期:2004-01-01 00:00:00

  • Autonomic control of the aging heart.

    abstract::Cardiovascular diseases including hypertension, myocardial infarction, stroke, and heart failure continue to account for the majority of deaths in the developed world. Whilst the incidence of these clinical disorders does increase with age, outcomes in affected patients tend to be disproportionately adverse with advan...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,评审

    doi:10.1007/s12017-008-8034-1

    authors: Kaye DM,Esler MD

    更新日期:2008-01-01 00:00:00

  • Mitochondrial UCP4 mediates an adaptive shift in energy metabolism and increases the resistance of neurons to metabolic and oxidative stress.

    abstract::The high-metabolic demand of neurons and their reliance on glucose as an energy source places them at risk for dysfunction and death under conditions of metabolic and oxidative stress. Uncoupling proteins (UCPs) are mitochondrial inner membrane proteins implicated in the regulation of mitochondrial membrane potential ...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1385/NMM:8:3:389

    authors: Liu D,Chan SL,de Souza-Pinto NC,Slevin JR,Wersto RP,Zhan M,Mustafa K,de Cabo R,Mattson MP

    更新日期:2006-01-01 00:00:00

  • Epigenome-wide association study for Parkinson's disease.

    abstract::A methylation-based EWAS on carefully phenotyped individuals with Parkinson's disease (PD) was conducted to reveal prioritised genes and pathways with statistically significant and sizable changes in PD and in the anxiety that often accompanies it. This was followed by subsequent replication of top-ranked CpG sites. U...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-014-8332-8

    authors: Moore K,McKnight AJ,Craig D,O'Neill F

    更新日期:2014-12-01 00:00:00

  • Renalase gene polymorphisms in patients with type 2 diabetes, hypertension and stroke.

    abstract::Renalase is a novel, recently identified, flavin adenine dinucleotide-dependent amine oxidase. It is secreted by the kidney and metabolizes circulating catecholamines. Renalase has significant hemodynamic effects, therefore it is likely to participate in the regulation of cardiovascular function.The aim of our study w...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-011-8158-6

    authors: Buraczynska M,Zukowski P,Buraczynska K,Mozul S,Ksiazek A

    更新日期:2011-12-01 00:00:00

  • Synaptogenesis: Modulation by Availability of Membrane Phospholipid Precursors.

    abstract::Phospholipids are the main constituents of brain membranes. Formation of new membranes requires that uridine, the omega-3 polyunsaturated fatty acids such as docosahexaenoic acid (DHA), and choline, the three circulating precursors of major phospholipids, interact via the Kennedy pathway. Supplementation of laboratory...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-016-8414-x

    authors: Cansev M

    更新日期:2016-09-01 00:00:00

  • Association Between NOS1 Gene Polymorphisms and Schizophrenia in Asian and Caucasian Populations: A Meta-Analysis.

    abstract::Schizophrenia is a complex psychiatric disorder characterized by memory impairments with delusions and hallucinations. Several investigations have focused on determining the association between NOS1 (nitric oxide synthase-1) polymorphisms and risk of schizophrenia (SZ). However, the association of rs2682826, rs3782206...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章,meta分析

    doi:10.1007/s12017-017-8460-z

    authors: Ahmed SSSJ,Akram Husain RS,Suresh Kumar,Ramakrishnan V

    更新日期:2017-09-01 00:00:00

  • Disregulation of Autophagy in the Transgenerational Cc2d1a Mouse Model of Autism.

    abstract::Autism spectrum disorder (ASD) is a heterogeneously childhood neurodevelopmental disorder, believed to be under development of various genetic and environmental factors. Autophagy and related pathways have also been implicated in the etiology of ASD. We aimed to investigate autophagic markers by generating the transge...

    journal_title:Neuromolecular medicine

    pub_type: 杂志文章

    doi:10.1007/s12017-019-08579-x

    authors: Dana H,Bayramov KK,Delibaşı N,Tahtasakal R,Bayramov R,Hamurcu Z,Sener EF

    更新日期:2020-06-01 00:00:00