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Journal articles on the topic 'Nitric oxide'

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Published: 4 June 2021

Last updated: 7 July 2024

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1

Kim, Youngsun, Donghee Choi, Hosun Jang, Changsu Na, Moonhyeon Hwang, Joohyun Cho, Kyoungin Lee, Sunmin Kim, Byoungsik Pyo, and Daehwan Youn. "Effects of Acupuncture at ST41, BL60, GB38 on Changes of Nitric Oxide and Nitric Oxide Synthase in Rats." Korean Journal of Acupuncture 30, no. 2 (June 27, 2013): 97–103. http://dx.doi.org/10.14406/acu.2013.30.2.097.

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2

Han, Ji young, Younghwa Kim, Jeehye Sung, Yurry Um, Yi Lee, and Junsoo Lee. "Suppressive Effects of Chrysanthemum zawadskii var. latilobum Flower Extracts on Nitric Oxide Production and Inducible Nitric Oxide Synthase Expression." Journal of the Korean Society of Food Science and Nutrition 38, no. 12 (December 31, 2009): 1685–90. http://dx.doi.org/10.3746/jkfn.2009.38.12.1685.

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3

Ushamohan, B. P., Aravind Kumar Rajasekaran, Yamini Keshavaprasad Belur, Judu Ilavarasu, and T. M. Srinivasan. "Nitric Oxide, Humming and Bhramari Pranayama." Indian Journal Of Science And Technology 16, no. 5 (February 5, 2023): 377–84. http://dx.doi.org/10.17485/ijst/v16i5.1212.

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4

Burke-Martindale, CH. "Inhaled nitric oxide therapy for adult respiratory distress syndrome." Critical Care Nurse 18, no. 6 (December 30, 1998): 21–27. http://dx.doi.org/10.4037/ccn1998.18.6.21.

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The selective pulmonary vasodilatory effects of inhaled nitric oxide decrease pulmonary artery hypertension and improve arterial oxygenation in patients with ARDS without causing concomitant systemic vasodilation. Inhaled nitrix oxide therapy may decrease the prevalence of pulmonary edema, pulmonary barotrauma, and oxygen toxicity that occur with current ARDS treatment. The effect of nitric oxide on oxygenation and pulmonary artery pressure may allow more time for the lungs to recover. Initial results of clinical trials are encouraging; however, the impact of inhaled nitric oxide therapy on patients with ARDS remains unclear. Further research is needed to develop safe delivery systems and monitoring techniques for routine clinical use, to determine potential adverse and toxic effects of nitric oxide therapy on patients, and to determine the effects of long-term exposure to nitric oxide among healthcare workers. Concomitant administration of other medications with inhaled nitric oxide should also be investigated.

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5

yu, Hai Bo, Li Feng Ding, Ren Fei Wang, and Liu Lian. "The Research Progress of Nitric Oxides Controlling Technology." Advanced Materials Research 955-959 (June 2014): 2481–86. http://dx.doi.org/10.4028/www.scientific.net/amr.955-959.2481.

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Because of the special physic-chemical characters of the nitric oxides, controlling of the nitric oxides which shaped during combustion is a complex technology. In this paper, the advance in emission controlling technology of nitric oxide has been reviewed.Selective catalytic reaction of the nitric oxide(SCR) and plasma process in denitration of flue gas are emphasized.

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6

Danylovych, G. V., T. V. Bohach, and Yu V. Danylovych. "The biosynthesis of nitric oxide from L-arginine. Nitric oxide formation features and its functional role in mitochondria." Ukrainian Biochemical Journal 90, no. 1 (February 15, 2018): 3–24. http://dx.doi.org/10.15407/ubj90.01.003.

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7

&NA;. "Nitric oxide." Reactions Weekly &NA;, no. 547 (April 1995): 8. http://dx.doi.org/10.2165/00128415-199505470-00026.

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8

&NA;. "Nitric oxide." Reactions Weekly &NA;, no. 465 (August 1993): 10. http://dx.doi.org/10.2165/00128415-199304650-00043.

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9

&NA;. "Nitric oxide." Reactions Weekly &NA;, no. 623 (October 1996): 10. http://dx.doi.org/10.2165/00128415-199606230-00028.

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10

&NA;. "Nitric oxide." Reactions Weekly &NA;, no. 629 (November 1996): 9. http://dx.doi.org/10.2165/00128415-199606290-00023.

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11

&NA;. "Nitric oxide." Reactions Weekly &NA;, no. 672 (October 1997): 9. http://dx.doi.org/10.2165/00128415-199706720-00025.

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12

&NA;. "Nitric oxide." Reactions Weekly &NA;, no. 898 (April 2002): 10. http://dx.doi.org/10.2165/00128415-200208980-00031.

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13

Fernández-Marcos, María, Luis Sanz, and Óscar Lorenzo. "Nitric oxide." Plant Signaling & Behavior 7, no. 2 (February 2012): 196–200. http://dx.doi.org/10.4161/psb.18895.

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14

Yang, Zhi-Lu, Qiang Zhao, and Qian-Jun He. "Nitric oxide." Medical Gas Research 9, no. 4 (2019): 0. http://dx.doi.org/10.4103/2045-9912.273953.

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15

&NA;. "Nitric oxide." Reactions Weekly &NA;, no. 511 (July 1994): 9. http://dx.doi.org/10.2165/00128415-199405110-00038.

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16

&NA;. "Nitric oxide." Reactions Weekly &NA;, no. 1338 (February 2011): 27–28. http://dx.doi.org/10.2165/00128415-201113380-00090.

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17

Papadakos, Peter J. "Nitric Oxide." Critical Care Medicine 27, no. 4 (April 1999): 847. http://dx.doi.org/10.1097/00003246-199904000-00054.

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18

Dellinger, R. Phillip, Janice L. Zimmerman, Robert W. Taylor, and Richard C. Straube. "Nitric Oxide." Critical Care Medicine 27, no. 4 (April 1999): 847–48. http://dx.doi.org/10.1097/00003246-199904000-00055.

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19

Toda, Noboru, Hiroshi Toda, Yoshio Hatano, and David C. Warltier. "Nitric Oxide." Anesthesiology 107, no. 5 (November 1, 2007): 822–42. http://dx.doi.org/10.1097/01.anes.0000287213.98020.b6.

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There has been an explosive increase in the amount of interesting information about the physiologic and pathophysiologic roles of nitric oxide in cardiovascular, nervous, and immune systems. The possible involvement of the nitric oxide-cyclic guanosine monophosphate pathway in the effects of anesthetic agents has been the focus of many investigators. Relaxations of cerebral and peripheral arterial smooth muscle as well as increases in cerebral and other regional blood flows induced by anesthetic agents are mediated mainly via nitric oxide released from the endothelium and/or the nitrergic nerve and also via prostaglandin I2 or endothelium-derived hyperpolarizing factor. Preconditioning with volatile anesthetics protects against ischemia-reperfusion-induced myocardial dysfunction and cell death or neurotoxicity, possibly through nitric oxide release. Inhibition of nitric oxide synthase decreases the anesthetic requirement. Involvement of nitric oxide in the effects of volatile, intravenous, and local anesthetics differs. This review article includes a summary of information about the sites and mechanisms by which various anesthetic agents interact with the nitric oxide-cyclic guanosine monophosphate system.

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20

GIACOIA, GEORGE P. "Nitric Oxide." Southern Medical Journal 88, no. 1 (January 1995): 33–41. http://dx.doi.org/10.1097/00007611-199501000-00004.

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21

Kubes, Paul. "NITRIC OXIDE." Shock 5, no. 2 (February 1996): 156. http://dx.doi.org/10.1097/00024382-199602000-00014.

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22

Matsuyama, Yukihiro, Koji Sato, Mitsuhiro Kamiya, Jyunji Yano, Hisashi Iwata, and Ken-ichi Isobe. "Nitric Oxide." Journal of Spinal Disorders 11, no. 3 (June 1998): 248???252. http://dx.doi.org/10.1097/00002517-199806000-00013.

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23

Laughlin, M. Harold. "NITRIC OXIDE." Medicine & Science in Sports & Exercise 35, Supplement 1 (May 2003): S2. http://dx.doi.org/10.1097/00005768-200305001-00005.

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24

MOHANAKUMAR, KOCHUPURACKAL P., BOBBY THOMAS, SUDARSHANA M. SHARMA, DHANASEKHARAN MURALIKRISHNAN, RUKHSANA CHOWDHURY, and CHUANG C. CHIUEH. "Nitric Oxide." Annals of the New York Academy of Sciences 962, no. 1 (May 2002): 389–401. http://dx.doi.org/10.1111/j.1749-6632.2002.tb04083.x.

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25

Salvemini, Daniela, Emanuela Masini, Alessandra Pistelli, Pier Francesco Mannaioni, and John Vane. "Nitric Oxide." Journal of Cardiovascular Pharmacology 17, Supplement (1991): 258???264. http://dx.doi.org/10.1097/00005344-199100001-00046.

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26

Garcia, Xiomara, and Fernando Stein. "Nitric Oxide." Seminars in Pediatric Infectious Diseases 17, no. 2 (April 2006): 55–57. http://dx.doi.org/10.1053/j.spid.2006.04.002.

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27

Cutrer, F. Michael. "Nitric Oxide." Headache Currents 1, no. 1 (July 2004): 14–15. http://dx.doi.org/10.1111/j.1743-5013.2004.10101b.x.

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28

Schroeder, Rebecca A., and Paul C. Kuo. "Nitric Oxide." Anesthesia & Analgesia 81, no. 5 (November 1995): 1052–59. http://dx.doi.org/10.1097/00000539-199511000-00027.

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29

Schroeder, Rebecca A., and Paul C. Kuo. "Nitric Oxide." Anesthesia & Analgesia 81, no. 5 (November 1995): 1052–59. http://dx.doi.org/10.1213/00000539-199511000-00027.

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30

Buisson, A., N. Lakhmeche, C. Verrecchia, M. Plotkine, and R. G. Boulu. "Nitric oxide." NeuroReport 4, no. 4 (April 1993): 444–46. http://dx.doi.org/10.1097/00001756-199304000-00027.

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31

Shen, Weiqun, Thomas H. Hintze, and Michael S. Wolin. "Nitric Oxide." Circulation 92, no. 12 (December 15, 1995): 3505–12. http://dx.doi.org/10.1161/01.cir.92.12.3505.

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32

Farrell, A. J., and D. R. Blake. "Nitric oxide." Annals of the Rheumatic Diseases 55, no. 1 (January 1, 1996): 7–20. http://dx.doi.org/10.1136/ard.55.1.7.

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33

Neufeld, Arthur H. "Nitric Oxide." Survey of Ophthalmology 43 (June 1999): S129—S135. http://dx.doi.org/10.1016/s0039-6257(99)00010-7.

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34

Huang, Emily P. "Nitric oxide." Current Biology 9, no. 2 (January 1999): R42. http://dx.doi.org/10.1016/s0960-9822(99)80004-9.

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35

Robbins, Richard A., and Matthew B. Grisham. "Nitric oxide." International Journal of Biochemistry & Cell Biology 29, no. 6 (June 1997): 857–60. http://dx.doi.org/10.1016/s1357-2725(96)00167-7.

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36

Norman, Jane E., and Foo Y. Liew. "Nitric oxide." Molecular Medicine Today 1, no. 8 (November 1995): 358. http://dx.doi.org/10.1016/s1357-4310(95)93796-x.

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37

Falkos, Sheryl A., Thomas A. Nakagawa, Anne P. M. C. De Jaegere, Frans I. M. Jacobs, Nico G. C. Laheij, John N. van den Anker, Jörg Dötsch, et al. "Nitric oxide." Intensive Care Medicine 22, S2 (June 1996): S175—S176. http://dx.doi.org/10.1007/bf03216379.

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38

Markhorst, D. G., T. Leenhoven, A. J. van Vught, J. López-Herce, A. Carrillo, A. Alcaraz, R. Moral, et al. "Nitric oxide." Intensive Care Medicine 22, S2 (June 1996): S224—S226. http://dx.doi.org/10.1007/bf03216399.

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39

Star, Robert A. "Nitric Oxide." American Journal of the Medical Sciences 306, no. 5 (November 1993): 348–58. http://dx.doi.org/10.1097/00000441-199311000-00015.

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40

Salvemini, Daniela, Emanuela Masini, Alessandra Pistelli, Pier Francesco Mannaioni, and John Vane. "Nitric Oxide." Journal of Cardiovascular Pharmacology 17, Supplement 3 (1991): S258—S264. http://dx.doi.org/10.1097/00005344-199117003-00047.

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41

Piedrafita, D., and F. Y. Liew. "Nitric oxide." Reviews in Medical Microbiology 9, no. 4 (October 1998): 179–90. http://dx.doi.org/10.1097/00013542-199810000-00001.

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42

Young, Duncan. "Nitric oxide." BJA CEPD Reviews 2, no. 6 (December 2002): 161–64. http://dx.doi.org/10.1093/bjacepd/02.06.161.

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43

MURRELL, GEORGE A. C., MARTIN M. DOLAN, DANIEL JANG, CSABA SZABO, RUSSELL F. WARREN, and JO A. HANNAFIN. "Nitric Oxide." Journal of Bone & Joint Surgery 78, no. 2 (February 1996): 265–74. http://dx.doi.org/10.2106/00004623-199602000-00014.

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44

Nahavandi, Masoud, Melville Q. Wyche, Keith Hunter, and Iroka J. Udeinya. "NITRIC OXIDE." Anesthesiology 89, Supplement (September 1998): 197A. http://dx.doi.org/10.1097/00000542-199809050-00009.

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45

Lindsay, Gregory, Louis Diamond, David C. Thompson, Sue M. Cibulsky, and Ralph J. Altiere. "Nitric Oxide." Chest 107, no. 3 (March 1995): 125S. http://dx.doi.org/10.1378/chest.107.3_supplement.125s.

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46

Wang, Ping. "Nitric Oxide." Archives of Surgery 129, no. 11 (November 1, 1994): 1137. http://dx.doi.org/10.1001/archsurg.1994.01420350035003.

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47

Milner, Anthony David. "Nitric oxide." European Journal of Pediatrics 153, S2 (February 1994): S7—S11. http://dx.doi.org/10.1007/bf02179666.

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48

Misra, A. N., M. Misra, and R. Singh. "Nitric oxide ameliorates stress responses in plants." Plant, Soil and Environment 57, No. 3 (March 4, 2011): 95–100. http://dx.doi.org/10.17221/202/2010-pse.

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Nitric oxide (NO) is a gaseous diatomic molecule with a wide variety of physiological and pathological implications in plants. Presence of unpaired electron in its molecular orbital makes it highly reactive; it can react directly with metal complexes, radicals, DNA, proteins, lipids and other biomolecules. Nitric oxide (NO) and reactive oxygen species (ROS) are known to play essential role in a number of important plant physiological processes. This manuscript reviews the role of NO on these processes during various biotic and abiotic stresses.  

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49

Li, J., B. Shi, S. Yan, L. Jin, Y. Guo, and T. Li. "Effects of chitosan on nitric oxide production and inducible nitric oxide synthase activity and mRNA expression in weaned piglets." Czech Journal of Animal Science 60, No. 8 (April 9, 2018): 359–66. http://dx.doi.org/10.17221/8405-cjas.

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The effects of chitosan on nitric oxide (NO) production and inducible nitric oxide synthase (iNOS) activity and gene expression in vivo or vitro were investigated in weaned piglets. In vivo, 180 weaned piglets were assigned to five dietary treatments with six replicates. The piglets were fed on a basal diet supplemented with 0 (control), 100, 500, 1000, and 2000 mg chitosan/kg feed, respectively. In vitro, the peripheral blood mononuclear cells (PBMCs) from a weaned piglet were cultured respectively with 0 (control), 40, 80, 160, and 320 µg chitosan/ml medium. Results showed that serum NO concentrations on days 14 and 28 and iNOS activity on day 28 were quadratically improved with increasing chitosan dose (P < 0.05). The iNOS mRNA expressions were linearly or quadratically enhanced in the duodenum on day 28, and were improved quadratically in the jejunum on days 14 and 28 and in the ileum on day 28 (P < 0.01). In vitro, the NO concentrations, iNOS activity, and mRNA expression in unstimulated PBMCs were quadratically enhanced by chitosan, but the improvement of NO concentrations and iNOS activity by chitosan were markedly inhibited by N-(3-[aminomethyl] benzyl) acetamidine (1400w) (P < 0.05). Moreover, the increase of NO concentrations, iNOS activity, and mRNA expression in PBMCs induced by lipopolysaccharide (LPS) were suppressed significantly by chitosan (P < 0.05). The results indicated that the NO concentrations, iNOS activity, and mRNA expression in piglets were increased by feeding chitosan in a dose-dependent manner. In addition, chitosan improved the NO production in unstimulated PBMCs but inhibited its production in LPS-induced cells, which exerted bidirectional regulatory effects on the NO production via modulated iNOS activity and mRNA expression.

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50

Lee, Alexandra, and Warwick Butt. "Nitric oxide: a new role in intensive care." Critical Care and Resuscitation 22, no. 1 (March 2, 2020): 72–79. http://dx.doi.org/10.51893/2020.1.sr1.

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Inhaled nitric oxide has been used for 30 years to improve oxygenation and decrease pulmonary vascular resistance. In the past 15 years, there has been increased understanding of the role of endogenous nitric oxide on cell surface receptors, mitochondria, and intracellular processes involving calcium and superoxide radicals. This has led to several animal and human experiments revealing a potential role for administered nitric oxide or nitric oxide donors in patients with systemic inflammatory response syndrome or ischaemia–reperfusion injury, and in patients for whom exposure of blood to artificial surfaces has occurred.

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