GLORIA

GEOMAR Library Ocean Research Information Access

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    Online Resource
    Online Resource
    American Physiological Society ; 2023
    In:  Physiology Vol. 38, No. S1 ( 2023-05)
    In: Physiology, American Physiological Society, Vol. 38, No. S1 ( 2023-05)
    Abstract: Calcium-activated chloride (Cl Ca ) channels play a key role in generating pacemaker currents responsible for maintaining motility in the phasic smooth muscle of the gastrointestinal tract. These channels may play a similar role in the urinary bladder, resulting in the bladder exhibiting spontaneous phasic contractions. These phasic contractions are known to underlie non-voiding contractions and transient pressure events. The purpose of this study was to determine whether the putative Cl Ca channel inhibitor benzbromarone has an inhibitory effect on transient pressure events in the isolated perfused mouse urinary bladder. We hypothesized benzbromarone would abolish bladder transient pressure events. Urinary bladders were isolated from male C57Bl6/J mice (7-8 wks old, 23.2-24.5 g body weight) post-euthanasia. Isolated bladders were placed in ice-cold nominally Ca-free dissection solution. Ureters were tied off, the bladder was cannulated through the urethra, and submerged in an organ bath containing physiological saline solution (37 °C, pH 7.4). The bladder was then attached to a syringe pump and inline pressure transducer to infuse at a constant rate of 1.8 mL/hr while recording intraluminal pressure. Urinary bladders were filled until they reached an intravesical pressure of 25 mmHg, which was defined as bladder capacity. Upon reaching bladder capacity, the bladder was emptied through the urethral cannula. Three fills were performed under baseline conditions to establish a consistent pressure-volume relationship. Benzbromarone (10 μM) was applied for 20 minutes. Bladders were subsequently filled to 80 % capacity and transient pressure events allowed to stabilize for at least 5 minutes. Transient pressure events were recorded in the absence and presence of benzbromarone. Transient pressure event frequency, amplitude, and duration were analyzed using a custom MatLab algorithm. Under baseline conditions, transient pressure events occurred at a frequency of 5.2 ± 0.8 events per minute (n = 3). Inhibition of Cl Ca with benzbromarone decreased transient pressure event frequency to 2.1±1.1 events per minute (n = 3, p = 0.08, paired t-test). Similarly, benzbromarone decreased transient pressure event amplitude from a baseline value of 0.22 ± 0.02 mmHg (n = 3) to 0.06 ± 0.04 mmHg (n = 3, p = 0.17, paired t-test). Transient pressure event duration was unaffected by benzbromarone (baseline duration 5.3 ± 0.3 sec, benzbromarone duration 5.2 ± 2.7 sec, n = 3, p= 0.98, paired t-test). In summary, we found that the putativeCl Ca channel inhibitor benzbromarone disrupted the rhythmicity and amplitude of transient pressure events, while leaving the duration of these contractile events unaltered. This suggests that Cl Ca channels play a role in generating the rhythm of phasic smooth muscle contractions in the bladder. The cellualr and molecular basis underlying the involvement of Cl Ca channels in the urinary bladder remains to be explored. This work was supported by a grant from the National Institute of Diabetes and Digestive and Kidney Diseases (R01DK125543). This is the full abstract presented at the American Physiology Summit 2023 meeting and is only available in HTML format. There are no additional versions or additional content available for this abstract. Physiology was not involved in the peer review process.
    Type of Medium: Online Resource
    ISSN: 1548-9213 , 1548-9221
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2023
    detail.hit.zdb_id: 3115360-4
    detail.hit.zdb_id: 2005759-3
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Online Resource
    Online Resource
    American Physiological Society ; 2023
    In:  Physiology Vol. 38, No. S1 ( 2023-05)
    In: Physiology, American Physiological Society, Vol. 38, No. S1 ( 2023-05)
    Abstract: The urothelium is thought to exert a direct influence on urinary bladder smooth muscle (UBSM) contractility by releasing active agents such as acetylcholine, ATP, and nitric oxide. Previous studies suggest that urothelial cells express muscarinic receptors, and upon stimulation, factors released from the urothelium may modulate UBSM contractility in response to muscarinic receptor activation on UBSM. This study aimed to determine whether the urinary bladder urothelium affects the contractility of UBSM in response to muscarinic stimulation. We hypothesized that the muscarinic receptor-induced contractile response of UBSM would be attenuated in the presence of the urothelium.Urinary bladders were isolated from male C57Bl6/J mice post-euthanasia. After dissection, bladders were placed in ice-cold nominally Ca2+-free dissection solution. Urinary bladders were opened and cut into strips with and without the urothelium. Strips were placed in myograph tissue baths (DMT) with physiological saline solution for contractility analysis. Each strip was stretched to 1g and was left to equilibrate for 45 minutes (min). Strips were washed 2-3x before applying carbachol (CCh). CCh was applied at concentrations of 0.001 μM, 0.01 μM, 0.1 μM,1 μM, and 10 μM with at least a 5-min waiting period between doses. [GH1] Contractile responses were analyzed using LabChart software and GraphPad Prism. Data were analyzed using a 2-way ANOVA with Tukey’s test for multiple comparisons. P 〈 0.05 was considered statistically significant. CCh induced a biphasic contraction in UBSM strips, which consisted of a rapid initial phasic contraction followed by a smaller stable elevation in tone. In strips without the urothelium (n=16 strips from 8 mice), peak contractions were 0.069 ± 0.104, 0.087 ± 0.102, 0.335 ± 0.302, 0.992 ± 0.606, and 1.197 ± 0.636 g in concentrations 0.001 μM, 0.01 μM, 0.1 μM, 1 μM, and 10 μM of CCh, respectively. In urothelium-denuded strips (n=15 strips from 8 mice), peak contractions were 0.054 ± 0.132, 0.077 ± 0.160, 0.365 ± 0.323, 1.222 ± 0.791, 1.416 ± 1.075 g across the same CCh concentration range. There were no significant differences in peak contraction responses to CCh at any concentration between urothelium-intact and -denuded UBSM strips (P = 0.2809). Similar results were obtained when quantifying steady-state contraction amplitudes. The contractile response to the muscarinic agent CCh in UBSM strips is not altered by the presence of the urothelium. This finding is in contrast with previous studies, and it suggests that muscarinic receptor stimulation on urothelial cells does not alter the contractile response induced by the activation of muscarinic receptors in the UBSM. This work was supported by a grant from the National Institute of Diabetes and Digestive and Kidney Diseases (R01DK125543). This is the full abstract presented at the American Physiology Summit 2023 meeting and is only available in HTML format. There are no additional versions or additional content available for this abstract. Physiology was not involved in the peer review process.
    Type of Medium: Online Resource
    ISSN: 1548-9213 , 1548-9221
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2023
    detail.hit.zdb_id: 3115360-4
    detail.hit.zdb_id: 2005759-3
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Online Resource
    Online Resource
    American Physiological Society ; 2005
    In:  American Journal of Physiology-Endocrinology and Metabolism Vol. 288, No. 5 ( 2005-05), p. E1002-E1010
    In: American Journal of Physiology-Endocrinology and Metabolism, American Physiological Society, Vol. 288, No. 5 ( 2005-05), p. E1002-E1010
    Abstract: Hyperhomocysteinemia is an independent risk factor for cardiovascular disorders. Elevated plasma homocysteine (Hcy) concentration is associated with other cardiovascular risk factors. We previously reported that Hcy stimulated cholesterol biosynthesis in HepG2 cells. In the present study, we investigated the underlying mechanisms of Hcy-induced hepatic cholesterol biosynthesis in an animal model. Hyperhomocysteinemia was induced in Sprague-Dawley rats by feeding a high-methionine diet for 4 wk. The mRNA expression and the enzyme activity of 3-hydroxy-3-methylglutaryl coenzyme A (HMG-CoA) reductase were significantly increased in livers of hyperhomocysteinemic rats. There were marked hepatic lipid accumulation and an elevation of plasma cholesterol concentration in hyperhomocysteinemic rats. Three transcription factors, namely, sterol regulatory element-binding protein-2 (SREBP-2), cAMP response element-binding protein (CREB), and nuclear factor Y (NF-Y) were activated in livers of hyperhomocysteinemic rats. Upon Hcy treatment of hepatocytes, there was a significant increase in HMG-CoA reductase mRNA expression in these cells. The activation of SREBP-2, CREB, and NF-Y preceded the increase in HMG-CoA reductase expression in Hcy-treated cells. Pretreatment of hepatocytes with inhibitors for transcription factors not only blocked the activation of SREBP-2, CREB, and NF-Y but also attenuated Hcy-induced HMG-CoA reductase mRNA expression. These results suggested that hyperhomocysteinemia-induced activation of SREBP-2, CREB, and NF-Y was responsible for increased cholesterol biosynthesis by transcriptionally regulating HMG-CoA reductase expression in the liver leading to hepatic lipid accumulation and subsequently hypercholesterolemia. In conclusion, the stimulatory effect of Hcy on hepatic cholesterol biosynthesis may represent an important mechanism for hepatic lipid accumulation and cardiovascular disorder associated with hyperhomocysteinemia.
    Type of Medium: Online Resource
    ISSN: 0193-1849 , 1522-1555
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2005
    detail.hit.zdb_id: 1477331-4
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    In: American Journal of Physiology-Endocrinology and Metabolism, American Physiological Society, Vol. 289, No. 1 ( 2005-07), p. E30-E39
    Abstract: Insulin resistance in skeletal muscle and heart plays a major role in the development of type 2 diabetes and diabetic heart failure and may be causally associated with altered lipid metabolism. Hormone-sensitive lipase (HSL) is a rate-determining enzyme in the hydrolysis of triglyceride in adipocytes, and HSL-deficient mice have reduced circulating fatty acids and are resistant to diet-induced obesity. To determine the metabolic role of HSL, we examined the changes in tissue-specific insulin action and glucose metabolism in vivo during hyperinsulinemic euglycemic clamps after 3 wk of high-fat or normal chow diet in awake, HSL-deficient (HSL-KO) mice. On normal diet, HSL-KO mice showed a twofold increase in hepatic insulin action but a 40% decrease in insulin-stimulated cardiac glucose uptake compared with wild-type littermates. High-fat feeding caused a similar increase in whole body fat mass in both groups of mice. Insulin-stimulated glucose uptake was reduced by 50–80% in skeletal muscle and heart of wild-type mice after high-fat feeding. In contrast, HSL-KO mice were protected from diet-induced insulin resistance in skeletal muscle and heart, and these effects were associated with reduced intramuscular triglyceride and fatty acyl-CoA levels in the fat-fed HSL-KO mice. Overall, these findings demonstrate the important role of HSL on skeletal muscle, heart, and liver glucose metabolism.
    Type of Medium: Online Resource
    ISSN: 0193-1849 , 1522-1555
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2005
    detail.hit.zdb_id: 1477331-4
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    Online Resource
    Online Resource
    American Physiological Society ; 2022
    In:  American Journal of Physiology-Regulatory, Integrative and Comparative Physiology Vol. 323, No. 5 ( 2022-11-01), p. R682-R693
    In: American Journal of Physiology-Regulatory, Integrative and Comparative Physiology, American Physiological Society, Vol. 323, No. 5 ( 2022-11-01), p. R682-R693
    Abstract: Storage and voiding functions in urinary bladder are well-known, yet fundamental physiological events coordinating these behaviors remain elusive. We sought to understand how voiding function is influenced by the rate at which the bladder fills. We hypothesized that faster filling rates would increase afferent sensory activity and increase micturition rate. In vivo, this would mean animals experiencing faster bladder filling would void more frequently with smaller void volumes. To test this hypothesis, we measured afferent nerve activity during different filling rates using an ex vivo mouse bladder preparation and assessed voiding frequency in normally behaving mice noninvasively (UroVoid). Bladder afferent nerve activity depended on the filling rate, with faster filling increasing afferent nerve activity at a given volume. Voiding behavior in vivo was measured in UroVoid cages. Male and female mice were given access to tap water or, to induce faster bladder filling rates, water containing 5% sucrose. Fluid intake increased dramatically in mice consuming 5% sucrose. As expected, micturition frequency was elevated in the sucrose group. However, even with the greatly increased rate of urine production, void volumes were unchanged in both genders. Although faster filling rates generated higher afferent nerve rates ex vivo, this did not translate into more frequent, smaller-volume voids in vivo. This suggests afferent nerve activity is only one factor contributing to the switch from bladder filling to micturition. Together with afferent nerve activity, higher centers in the central nervous system and the state of arousal are likely critical to coordinating the micturition reflex.
    Type of Medium: Online Resource
    ISSN: 0363-6119 , 1522-1490
    Language: English
    Publisher: American Physiological Society
    Publication Date: 2022
    detail.hit.zdb_id: 1477297-8
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    Online Resource
    Online Resource
    American Physiological Society ; 1998
    In:  Physiology Vol. 13, No. 6 ( 1998-12), p. 287-293
    In: Physiology, American Physiological Society, Vol. 13, No. 6 ( 1998-12), p. 287-293
    Abstract: Endothelial cells exposed to inductive central nervous system factors differentiate into a blood-brain barrier phenotype. The blood-brain barrier frequently obstructs the passage of chemotherapeutics into the brain. Tissue culture systems have been developed to reproduce key properties of the intact blood-brain barrier and to allow for testing of mechanisms of transendothelial drug permeation.
    Type of Medium: Online Resource
    ISSN: 1548-9213 , 1548-9221
    Language: English
    Publisher: American Physiological Society
    Publication Date: 1998
    detail.hit.zdb_id: 3115360-4
    detail.hit.zdb_id: 2005759-3
    SSG: 12
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...