Showing posts with label adjuvant therapy. Show all posts
Showing posts with label adjuvant therapy. Show all posts

Thursday, 28 August 2025

Probiotics as an Adjuvant Treatment for Psychiatric Disorders | chapter 12 | Medical Research and Its Applications Vol. 9

 

Introduction: Many psychiatric illnesses have been linked to the gut microbiome, with supplements such as probiotics showing some efficacy in alleviating the symptoms of some psychiatric illnesses. There is a well-established, bidirectional connection between the gut microbiome and the brain, known as the gut-brain-axis. Research suggests that the gut-brain-axis may influence a variety of neurological functions, including the pathology of psychiatric disorders. The aim of this chapter is to evaluate the current literature investigating the effects of adjuvant probiotic or synbiotic administration in combination with first-line treatments for psychiatric illnesses.

 

Methods: This review was carried out according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines. A systematic search of four databases was conducted using key terms related to treatments for psychiatric illnesses, the gut microbiome, and probiotics.

 

All results were then evaluated based on specific eligibility criteria.

 

Results: Ten studies met eligibility criteria and were analysed for reported changes in outcome measures used to assess the symptoms of psychiatric illness and the tolerability of treatment. All Major Depressive Disorder (MDD) (n=7) and Generalized Anxiety Disorder (GAD) (n=1) studies found adjuvant probiotic or synbiotic treatment to be more efficacious in improving the symptoms of psychiatric illness than the first-line treatment alone or with placebo. The schizophrenia studies (n=2) found adjuvant probiotic treatment to have no significant difference in clinical outcomes, but it was found to improve the tolerability of first-line antipsychotics.

 

Discussion and Conclusion: The findings of the studies included in this chapter suggest the use of adjuvant probiotic treatment with selective serotonin reuptake inhibitors (SSRIs) for MDD and GAD to be superior to SSRI treatment alone. Probiotic adjuvant treatment with antipsychotics could be beneficial for improving the tolerability of the antipsychotics, but these findings do not suggest that adjuvant probiotic treatment would result in improved clinical outcomes for symptoms of schizophrenia. Finally, it is said that the gut microbiome and the brain are clearly linked, and reviewed studies show that combining treatments that target both areas respectively is a viable and efficacious way to combat the symptoms and treat psychiatric illnesses.

 

 

Author(s) Details

E. Forth

Department of Psychiatry, Providence Care Hospital, Kingston, ON, Canada, Centre for Neuroscience Studies, Queen’s University, Kingston, ON, Canada and Department of Psychiatry, Queen’s University, Kingston ON, Canada.

B. Buehner

Centre for Neuroscience Studies, Queen’s University, Kingston, ON, Canada.

A. Storer

Centre for Neuroscience Studies, Queen’s University, Kingston, ON, Canada.

C. Sgarbossa

Department of Psychiatry, Providence Care Hospital, Kingston, ON, Canada, Centre for Neuroscience Studies, Queen’s University, Kingston, ON, Canada and Department of Psychiatry, Queen’s University, Kingston ON, Canada.

R. Milev

Department of Psychiatry, Providence Care Hospital, Kingston, ON, Canada, Centre for Neuroscience Studies, Queen’s University, Kingston, ON, Canada, Department of Psychiatry, Queen’s University, Kingston ON, Canada and Department of Psychology, Queen’s University, ON, Canada.

A. Chinna Meyyappan

Department of Psychiatry, Providence Care Hospital, Kingston, ON, Canada, Centre for Neuroscience Studies, Queen’s University, Kingston, ON, Canada and Department of Psychiatry, Queen’s University, Kingston ON, Canada.

 

Please see the book here:- https://doi.org/10.9734/bpi/mria/v9/1103

Thursday, 11 March 2021

An Assessment of Mistletoe-Based Drugs Work in Synergy with Radio-Chemotherapy in the Treatment of Glioma in vitro and in vivo in Glioblastoma Bearing Mice | Chapter 3 | Technological Innovation in Pharmaceutical Research Vol. 2

 In Europe, extracts from the mistletoe plant Viscum album L. (VE) have long been used in complementary cancer therapy. Several compounds, such as mistletoe lectins (ML) 1-3 and viscotoxins (VT), are contained in VE, as well as a few minor ingredients. ML-1 is thought to be the primary anti-tumor component of VE, VT causes cell death, and some minor compounds may enhance ML-1's anti-tumor function. ML can stimulate the immune system, cause cytotoxicity, change the expression of cancer-related genes, and influence tumour cell proliferation and motility. The anti-tumor effects of the VE ISCADOR Qu, recombinant ML-1 (Aviscumine), and native ML-1 in the treatment of glioblastoma (GBM), the most common brain tumour in adults, are investigated in this research. We also wanted to see whether a mistletoe-based therapy could have synergistic results when combined with temozolomide (TMZ) or irradiation as an adjuvant treatment. The drug-induced cytotoxicity is well correlated with the expression of the ML receptor CD75s, which is expressed in GBM specimens and cells but not in the normal brain. The drugs cause cell death in GBM cells in a concentration-dependent manner, trigger a G2/M phase arrest, and have synergistic and additive anti-tumor effects. GBM mice survived longer after a single intratumoral injection of Aviscumine than after tumour irradiation, and even better when combined with radio-chemotherapy. This suggests that using ML-containing drugs as an adjuvant therapy for glioma patients may be helpful.

Author (s) Details

Sonja Schötterl
Department of Science in Biochemistry, University Tuebingen, Germany.

Jennifer T. Miemietz
Molecular Neuro-Oncology, Hertie Institute for Clinical Brain Research and Center Neurology, University of Tübingen, Otfried-Müller-Str. 27, 72076 Tübingen, Germany.

Elena I. Ilina
Luxembourg Centre of Neuropathology (LCNP), Luxembourg; 1, Rue Louis Rech, L-3555 Dudelange, Luxembourg and NORLUX Neuro-Oncology Laboratory, Luxembourg Institute of Health, Luxembourg; 84, Rue Val Fleuri, L-1526 Luxembourg, Luxembourg.

Naita M. Wirsik
Neurological Institute (Edinger Institute), Goethe University Frankfurt, Heinrich-Hoffmann-Str. 7, 60528 Frankfurt/Main, Germany.

Ingrid Ehrlich
Learning and Memory, Hertie Institute for Clinical Brain Research and Center Neurology, University of Tübingen, Otfried-Müller-Str. 27, 72076 Tübingen, Germany.


Andrea Gall
Learning and Memory, Hertie Institute for Clinical Brain Research and Center Neurology, University of Tübingen, Otfried-Müller-Str. 27, 72076 Tübingen, Germany.

Stephan M. Huber
Department of Radiation Oncology, University Tübingen, Hoppe-Seyler-Str. 3, 72076 Tübingen, Germany.

Hans Lentzen
MELEMA Pharma GmbH, Hamburg, Germany.

Michel Mittelbronn
Luxembourg Centre of Neuropathology (LCNP), Luxembourg; 1, Rue Louis Rech, L-3555 Dudelange, Luxembourg and NORLUX Neuro-Oncology Laboratory, Luxembourg Institute of Health, Luxembourg; 84, Rue Val Fleuri, L-1526 Luxembourg, Luxembourg and Neurological Institute (Edinger Institute), Goethe University Frankfurt, Heinrich-Hoffmann-Str. 7, 60528 Frankfurt/Main, Germany and Laboratoire Nationale de Santé, Dudelange, 1, Rue Louis Rech, L-3555 Dudelange, Luxembourg and Luxembourg Centre for Systems Biomedicine (LCSB), University of Luxembourg, 7 Avenue des Hauts-Fourneaux, 4362 Esch-sur-Alzette, Luxembourg.

Prof. Dr. Ulrike Naumann
Molecular Neuro-Oncology, Hertie Institute for Clinical Brain Research and Center Neurology, University of Tübingen, Otfried-Müller-Str. 27, 72076 Tübingen, Germany.

View Book :- https://stm.bookpi.org/TIPR-V2/issue/view/55