Physician
Internal Medicine
Dr. Pawel Olszewski, MD
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Pawel Olszewski works in the field of Internal Medicine. He went to Jagiellonian University Medical College. He received 1 awards: "CMS Meaningful Use Stage 1 Certification". Dr. Pawel Olszewski is a published MD. He has 50 publications published. The most current publication "Oxytocin: a conditional anorexigen whose effects on appetite depend on the physiological, behavioral and social contexts." Pawel Olszewski accepts Medicare payments and is registered with Medicare.gov.
Publications
- Oxytocin: a conditional anorexigen whose effects on appetite depend on the physiological, behavioral and social contexts.
- Effect of oxytocin receptor blockade on appetite for sugar is modified by social context.
- A non-peptide oxytocin receptor agonist, WAY-267,464, alleviates novelty-induced hypophagia in mice: Insights into changes in c-Fos immunoreactivity.
- Functional relationship between oxytocin and appetite for carbohydrates versus saccharin.
- Oxytocin receptor blockade reduces acquisition but not retrieval of taste aversion and blunts responsiveness of amygdala neurons to an aversive stimulus.
- Inverse association of high-fat diet preference and anxiety-like behavior: a putative role for urocortin 2.
- Role of alpha-MSH in the regulation of consummatory behavior: immunohistochemical evidence.
- Identification of central sites involved in butorphanol-induced feeding in rats.
- Evidence of interactions between melanocortin and opioid systems in regulation of feeding.
- Paraventricular hypothalamic alpha-melanocyte-stimulating hormone and MTII reduce feeding without causing aversive effects.
- Opioids affect acquisition of LiCl-induced conditioned taste aversion: involvement of OT and VP systems.
- The effect of [Phe(1)psi(CH(2)-NH)Gly(2)]-nociceptin(1-13)NH(2) on feeding and c-Fos immunoreactivity in selected brain sites.
- Nocistatin inhibits food intake in rats.
- Fos expression in feeding-related brain areas following intracerebroventricular administration of orphanin FQ in rats.
- Dopamine D1 receptor gene expression decreases in the nucleus accumbens upon long-term exposure to palatable food and differs depending on diet-induced obesity phenoty...
- Functional coupling analysis suggests link between the obesity gene FTO and the BDNF-NTRK2 signaling pathway.
- Expression levels of genes encoding melanin concentrating hormone (MCH) and MCH receptor change in taste aversion, but MCH injections do not alleviate aversive responses.
- Comprehensive analysis of localization of 78 solute carrier genes throughout the subsections of the rat gastrointestinal tract.
- Opioids as facilitators of feeding: can any food be rewarding?
- Fto colocalizes with a satiety mediator oxytocin in the brain and upregulates oxytocin gene expression.
- Fto immunoreactivity is widespread in the rodent brain and abundant in feeding-related sites, but the number of Fto-positive cells is not affected by changes in energy...
- Molecular, immunohistochemical, and pharmacological evidence of oxytocin's role as inhibitor of carbohydrate but not fat intake.
- Oxytocin as feeding inhibitor: maintaining homeostasis in consummatory behavior.
- [Early results of proximal femoral fractures treated with FENIX modular hemiarthroplasty].
- Central nociceptin/orphanin FQ system elevates food consumption by both increasing energy intake and reducing aversive responsiveness.
- Chronic sugar intake dampens feeding-related activity of neurons synthesizing a satiety mediator, oxytocin.
- The obesity gene, TMEM18, is of ancient origin, found in majority of neuronal cells in all major brain regions and associated with obesity in severely obese children.
- Glutamate, aspartate and nucleotide transporters in the SLC17 family form four main phylogenetic clusters: evolution and tissue expression.
- Molecular mechanisms underlying anorexia nervosa: focus on human gene association studies and systems controlling food intake.
- Hypothalamic FTO is associated with the regulation of energy intake not feeding reward.
- Complexity of neural mechanisms underlying overconsumption of sugar in scheduled feeding: involvement of opioids, orexin, oxytocin and NPY.
- Analysis of the network of feeding neuroregulators using the Allen Brain Atlas.
- Ghrelin in the CNS: from hunger to a rewarding and memorable meal?
- The obesity gene, FTO, is of ancient origin, up-regulated during food deprivation and expressed in neurons of feeding-related nuclei of the brain.
- Alpha-melanocyte stimulating hormone and ghrelin: central interaction in feeding control.
- Intraventricular ghrelin activates oxytocin neurons: implications in feeding behavior.
- Central ghrelin induces feeding driven by energy needs not by reward.
- Central opioids and consumption of sweet tastants: when reward outweighs homeostasis.
- Effect of opioid receptor ligands injected into the rostral lateral hypothalamus on c-fos and feeding behavior.
- Functional interaction between nociceptin/orphanin FQ and alpha-melanocyte-stimulating hormone in the regulation of feeding.
- Intra-amygdalar injection of DAMGO: effects on c-Fos levels in brain sites associated with feeding behavior.
- Minireview: Characterization of influence of central nociceptin/orphanin FQ on consummatory behavior.
- Hypothalamic paraventricular injections of ghrelin: effect on feeding and c-Fos immunoreactivity.
- Neural basis of orexigenic effects of ghrelin acting within lateral hypothalamus.
- Agouti-related protein: appetite or reward?
- Effects of intracerebroventricular ethanol on ingestive behavior and induction of c-Fos immunoreactivity in selected brain regions.
- Peptides that regulate food intake: effect of peptide histidine isoleucine on consummatory behavior in rats.
- Effect of Agouti-related protein on development of conditioned taste aversion and oxytocin neuronal activation.
- Effect of nociceptin/orphanin FQ on food intake in rats that differ in diet preference.
Schools
Jagiellonian University Medical College Faculty Of Medicine
Henry Ford Hospital
Doctors Specialties
- Internal Medicine
Accepted Insurances
Awards
- CMS Meaningful Use Stage 1 Certification
Education
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Henry Ford Hospital - Wayne State University -
Jagiellonian University Medical College
Hospital
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Beloit Health System
Drug Facts
| NPI NUMBER | 1679582043 | |
| NPPES Provider LastName | OLSZEWSKI | |
| NPPES Provider FirstName | PAWEL | |
| NPPES Provider ZIPCode | 535111842 | |
| NPPES Provider State | WI | |
| Specialty Description | Internal Medicine | |
| Total Claim Count | 11060.0 | |
| Distinct Opioid Count | 5.0 | |
| Opioid Claim Count | 417.0 | |
| Percent Opioid Claims | 3.77 |
Helpful Reviews
Medicare Facts
| National Provider Identifier [NPI] | 1679582043 |
| Last Name Of The Provider | OLSZEWSKI |
| First Name Of The Provider | PAWEL |
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